Cobas U 601 Urine Analyzer: Operator's Manual Version 2.4 Software Version 2.3
Cobas U 601 Urine Analyzer: Operator's Manual Version 2.4 Software Version 2.3
Document information
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
3
Instrument approvals The cobas u 601 urine analyzer meets the requirements
laid down in:
• Directive 98/79/EC of the European Parliament and of
the Council of 27 October 1998 on in vitro diagnostic
medical devices
• Directive 2011/65/EU of the European Parliament and
of the Council of 8 June 2011 on the restriction of the
use of certain hazardous substances in electrical and
electronic equipment
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
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Contact address
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
Table of contents 5
Table of contents
7 Maintenance
Safety 283
Routine maintenance 284
Miscellaneous maintenance actions 287
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
6 Table of contents
Troubleshooting
8 Troubleshooting
Exceptional situations 301
Screenshots 303
Log files 304
No photometer calibration can be
generated 306
No measuring cell calibration can be
generated 306
Detached barcode labels 307
Recovering from an irregular stop 308
Emergency stop 309
When you have accidentally pulled the waste
drawer during operation 311
Recovering from a power outage 312
Safety interlock 314
Clogged inlet water filter 314
Blocked floats 317
Glossary
9 Glossary
Index
Index 327
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
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Preface
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cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
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Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
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Symbol Explanation
o List item.
Tip. Extra information on correct use or useful
q
hints.
Start of a procedure.
I Extra information within a task.
f Result of an action within a task.
d Materials that are required for a task.
j Prerequisites of a task.
Topic. Used in cross-references to topics and
u for related topics containing further
information.
Figure. Used in figure titles and cross-
w
references to figures.
Table. Used in table titles and cross-references
y
to tables.
y Symbols used in the publication
Symbol Comment
Safety alert.
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
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Symbol Comment
Global trade item number
Date of manufacture
Serial number
Abbreviation Explanation
A ampere
BIL bilirubin
CLA clarity
COL color
CSA Canadian Standards Association
CSV character separated values
e.g. exempli gratia – for example
EC European Community
EMC electromagnetic compatibility
EN European standard
ERY erythrocytes and hemoglobin
GLU glucose
Hz hertz
i.e. id est – that is to say
IEC International Electrical Commission
IVD in vitro diagnostic directive
KET ketones
LEU leukocytes
LAS laboratory automation system
LIS laboratory information system
max. maximum
min. minimum
mm millimeter
n/a not applicable
NIT nitrite
nm nanometer
PRO protein
QC quality control
y Abbreviations
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
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Abbreviation Explanation
RD Roche Diagnostics
RFID radio frequency identification
SG specific gravity
STAT short turn around time
UBG urobilinogen
UL Underwriters Laboratories Inc.
UPS uninterrupted power supply
V volt
VA volt-ampere
VAC volt alternating current
W watt
y Abbreviations
New control unit version The control unit was replaced with a new version (version
2).
Windows 10 operating system The internal PC uses the Windows 10 operating system.
Upgraded test strip tray and transporter The test strip tray and test strip transporter were
enhanced.
Replacing of reference plate The reference plate can only be replaced by a Roche
Service representative.
Illustrations and screenshots Illustrations and screenshots were adapted to reflect the
latest hardware and software.
Optional components Colored labels for Roche 5-position racks are now
available.
u Optional components (114)
Working with Sample sequence number mode The procedure for working with Sample sequence
number mode has been improved.
u Defining the sample sequence number ranges (156)
u Rerunning tests when working with Sample sequence
number mode (185)
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cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
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STAT and routine results are marked when If you work with Sample sequence number mode,
working with Sample sequence number mode sample IDs for routine test results are marked with an “N”
preceding the sample sequence number, and “E” for
STAT test results.
u Validating results (172)
Invalid SG results You can now search for invalid SG results and edit them
manually.
u Managing invalid SG results (176)
Working with Sample sequence number mode The information on defining the validation method has
been adapted.
u Defining the validation method (250)
Illustrations and screenshots Illustrations and screenshots were adapted to reflect the
latest hardware and software.
Automatic rack feed, input connection unit You can optionally connect the analyzer to a laboratory
automation system by replacing the input buffer with an
input connection unit. This allows automatic rack feed to
the analyzer.
u Input connection unit (76)
u Operation with input connection unit (164)
u To load a priority rack when working with an
LAS (167)
u To perform a QC measurement when working with an
LAS (225)
u To clean the inlet water filter (external water
supply) (316)
u To loosen the floats in the water container for external
water supply (318)
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cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
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External water supply You can optionally connect the analyzer to an external
laboratory water supply system. When using this feature,
the liquid waste is drained off directly to the laboratory
liquid waste system.
u Water container for external water supply (84)
u Liquid waste with external water supply (86)
u To clean the inlet water filter (external water
supply) (316)
u To loosen the floats in the water container for external
water supply (318)
Overview work area • The categorizing of the task list has been improved.
• An emergency stop button (E. Stop) was added. Use
this function if, for some reason, all activities on the
analyzer must be stopped immediately or if the
analyzer is stuck in either the Operating or Init
status.
• When working with a laboratory automation system,
the Priority rack button is available on the Overview
work area.
u Emergency stop (309)
u To load a priority rack when working with an
LAS (167)
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cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
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Printing and exporting information The feature was adapted and applied consistently.
Some changes:
• Screenshots are no longer part of the problem report,
instead, you can save them separately.
u Printing and exporting information, generating
reports (237)
Replacing the reference plate The description of how to replace the reference plate was
adjusted.
Warning intervals You can now define how long before the event a warning
is issued for expiry of materials and maintenance actions.
u Defining when notifications should be
generated (268)
Defining QC materials using the RFID reader The procedure for defining QC materials using the RFID
reader was adapted.
u To define a new QC material by reading the RFID
tag (227)
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cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
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Range tables and cross-check rules The procedures for defining range tables and cross-
check rules were simplified.
u Defining range tables (254)
u Defining cross-check rules (251)
Color ranges for COL You can now adjust the color ranges for COL to achieve
full correspondence with the actual color.
u Defining the ranges for the colors of COL (261)
Importing system settings You can now import system settings that were generated
using software versions other than the current one.
u Importing and exporting system settings (273)
Adjusting the probe action To enable the use of different racks and tubes, a function
is now provided to adjust the probe action to the changed
dimensions.
u To adjust the probe action (278)
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cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
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Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
System description
1 Safety .......................................................................................................................... 19
2 Introduction .............................................................................................................. 41
3 Hardware ................................................................................................................... 59
4 Software ...................................................................................................................117
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cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
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Table of contents
Safety 1
In this chapter 1
Safety classification . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Safety precautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
Operator qualification . . . . . . . . . . . . . . . . . . . . . . . 22
Safe and proper use of the analyzer . . . . . . . . . . . 22
Personal safety . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Personal protective equipment . . . . . . . . . . . . . 23
Accuracy and precision of measured results . 23
Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Environmental conditions . . . . . . . . . . . . . . . . . 24
Approved parts . . . . . . . . . . . . . . . . . . . . . . . . . . 24
Third-party software. . . . . . . . . . . . . . . . . . . . . . 24
Miscellaneous safety precautions . . . . . . . . . . . . . 24
Safety summary . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 26
Warning messages . . . . . . . . . . . . . . . . . . . . . . . . . . 26
Electrical safety . . . . . . . . . . . . . . . . . . . . . . . . . . 26
Biohazardous materials . . . . . . . . . . . . . . . . . . . 27
Waste . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
Barcode readers . . . . . . . . . . . . . . . . . . . . . . . . . 28
Foam, bubbles or films on sample . . . . . . . . . . 28
Data security . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
Caution messages . . . . . . . . . . . . . . . . . . . . . . . . . . 30
Mechanical safety. . . . . . . . . . . . . . . . . . . . . . . . 30
1 Safety
Working solutions . . . . . . . . . . . . . . . . . . . . . . . . 30
Insoluble contaminants in samples . . . . . . . . . 31
Influence of vibrations . . . . . . . . . . . . . . . . . . . . 31
Excessive ambient humidity . . . . . . . . . . . . . . . 31
Malfunction due to interfering
electromagnetic fields . . . . . . . . . . . . . . . . . . . . 32
Fatigue due to long hours of operation . . . . . . 32
Notices . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 32
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cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
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Table of contents
Moving parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
Fuses . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
Spillage. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
Excessive ambient humidity . . . . . . . . . . . . . . . 33
Influence of vibrations . . . . . . . . . . . . . . . . . . . . 34
Safety labels on the equipment . . . . . . . . . . . . . . . . . . 34
Analyzer views . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 34
Front view . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
Back view. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 36
Solid waste compartment . . . . . . . . . . . . . . . . . 37
Input connection unit . . . . . . . . . . . . . . . . . . . . . 38
Disposal of the equipment . . . . . . . . . . . . . . . . . . . . . . 39
1 Safety
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
Safety classification 21
Safety classification
This section explains how precautionary information is
presented in this manual.
! WARNING
Warning
r Indicates a hazardous situation which, if not avoided,
could result in death or serious injury.
! CAUTION
Caution
r Indicates a hazardous situation which, if not avoided,
could result in minor or moderate injury.
NOTICE
Notice
r Indicates a hazardous situation which, if not avoided,
could result in damage to equipment.
q Tip
1 Safety
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
22 Safety precautions
Safety precautions
! Generic hazard statements
In this section
Operator qualification (22)
Safe and proper use of the analyzer (22)
Miscellaneous safety precautions (24)
Operator qualification
Insufficient knowledge and skills Operators are required to have a sound knowledge of
relevant guidelines and standards as well as the
information and procedures contained in the Operator’s
Manual.
r Do not carry out operation and maintenance unless
you have been trained by Roche. Carefully follow the
procedures specified in the Operator’s Manual for the
operation and maintenance of the analyzer. Leave
maintenance, installation or service that is not
described in the Operator’s Manual to trained Roche
Service representatives. Follow Good Laboratory
Practices especially when working with biohazardous
material.
Installation (23)
Environmental conditions (24)
Approved parts (24)
Third-party software (24)
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
Safety precautions 23
Personal safety
Personal injury and infection due to sharps, r Good Laboratory Practice can reduce the risk of injury.
rough edges, and/or moving parts r Be aware of your laboratory environment, well-
prepared, and follow the instructions for use.
r Some areas of the instrument may have sharps, rough
edges, and/or moving parts.
Wear personal protective equipment to minimize the
risk of injury from bodily contact with such parts,
especially in less accessible areas, or while cleaning
the instrument.
r Your personal protective equipment should be
appropriate to the degree and type of potential
hazard, e.g. suitable lab gloves, eye protection, lab
coat, and footwear.
Installation
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
24 Safety precautions
Environmental conditions
Approved parts
Third-party software
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cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
Safety precautions 25
Analyzer unused for an extended period of If the analyzer is not used for an extended period of time,
time the power switch must be set to the off position. Observe
the onboard stability values for test strips.
1 Safety
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cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
26 Safety summary
Safety summary
This safety summary contains the most important and
general warning, caution, and notice messages.
Additionally, you will find specific safety information at
the beginning of chapters and with procedures.
In this section
Warning messages (26)
Caution messages (30)
Notices (32)
Warning messages
Electrical safety
Electrical shock by electronic equipment Removing the covers of electronic equipment can cause
electric shock, as there are high voltage parts inside.
r Do not attempt to work in any electronic
compartment.
r Do not remove any cover of the analyzer other than
those specified in this Operator’s Manual.
r Installation, service, and repair must only be
performed by personnel authorized and trained by
1 Safety
Roche.
r Observe the safety labels on the equipment.
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
Safety summary 27
Biohazardous materials
Infection by samples and associated Contact with samples containing material of human origin
materials may result in infection. All materials and mechanical
components associated with samples of human origin are
potentially biohazardous.
r Follow Good Laboratory Practices, especially when
working with biohazardous material.
r Keep the cover closed and in place during operation.
r Be sure to wear appropriate protective equipment,
including, but not limited to, eye protection with side
shields, fluid resistant lab coat, and approved lab
gloves.
r Wear a face shield if there is a chance of splash or
splatter.
r If any biohazardous material is spilled, wipe it up
immediately and apply disinfectant.
r If sample or liquid waste comes into contact with your
skin, wash it off immediately with soap and water and
apply disinfectant. Consult a physician.
Infection by injury due to sharp objects r When wiping probes, use several layers of tissue and
wipe from the top down.
r Be careful to not puncture yourself.
r Be sure to wear appropriate protective equipment, for
example gloves. Take extra care when working with
lab gloves; these can easily be pierced or cut, which
can lead to infection.
Waste
Infection by liquid waste Contact with liquid waste may result in infection. All
materials and mechanical components associated with
the waste systems are potentially biohazardous.
r Be sure to wear protective equipment. Take extra care
when working with lab gloves; these can easily be
pierced or cut, which can lead to infection.
1 Safety
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
28 Safety summary
Contamination of the environment by liquid The waste of the analyzer is potentially biohazardous and
and solid waste must be treated in accordance with the relevant laws and
regulations.
r When disposing of any waste, do so in accordance
with the appropriate local regulations.
r Any substances contained in QC materials and other
working materials, which are legally regulated for
environmental protection, must be disposed of in
accordance with the relevant water discharge facility
regulations. For the legal regulations on water
discharge, please contact the suppliers of the
materials.
Barcode readers
Barcode readers using LED technology with very low
output power are used to scan the barcodes on samples
and racks.
Loss of sight The intense light of the LEDs may damage your eyes.
r Do not stare into the LEDs.
Incorrect results due to incorrect sample Foam, bubbles or films on a sample or inside a sample
volume container may cause pipetting volume shortage and lead
to deterioration in measurement accuracy.
r When loading samples or QC materials on the
instrument, ensure that they do not contain foam,
bubbles or films.
1 Safety
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
Safety summary 29
Data security
Unauthorized access and data loss due to External storage devices can be infected with and
malicious software and hacker attacks transmit computer malware, which may be used to gain
unauthorized access to data or cause unwanted changes
to software.
The cobas u 601 urine analyzer is not protected against
malicious software and hacker attacks.
The customers are responsible for IT security of their IT
infrastructure and for protecting it against malicious
software and hacker attacks. Failure to do so may result
in data loss or render the cobas u 601 urine analyzer
unusable.
r Roche recommends the following precautions:
o Allow connection to authorized external devices
only.
o Ensure that all external devices are protected by
appropriate security software.
o Ensure that access to all external devices is
protected by appropriate security equipment.
Roche strongly recommends the use of a firewall
of Roche.
o Do not copy or install any software on the
cobas u 601 urine analyzer unless it is part of the
system software or you are instructed to do so by a
Roche Service representative.
o If additional software is required, contact your
Roche Service representative to ensure validation
of the software in question.
o Do not use the USB ports to connect other storage
devices unless you are instructed to do so by
official user documentation or a Roche Service
representative.
o Exercise utmost care when using external storage
devices such as CDs, or DVDs. Do not use them on
public or home computers while connecting to the
cobas u 601 urine analyzer.
o Keep all external storage devices in a secure place
and ensure that they can be accessed by
authorized persons only.
1 Safety
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
30 Safety summary
Caution messages
Mechanical safety
Personal injury due to contact with moving r Keep the main cover closed and in place while the
parts analyzer is operating.
r During operation and maintenance, proceed
according to the instructions contained in the
Operator’s Manual.
r Observe the safety labels on the equipment.
u Safety labels on the equipment (34)
Working solutions
Skin inflammation or injury caused by Direct contact with cleaning solutions or other working
working solutions solutions may cause skin irritation, inflammation, or
burns.
r If a cleaning solution or other working solution comes
into contact with your skin, wash it off immediately
with water and apply disinfectant. Consult a physician.
1 Safety
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
Safety summary 31
Incorrect results and interruption of analysis Insoluble contaminants in samples and bubbles or films
due to contaminated samples inside a sample container may cause clogging or
pipetting volume shortage and lead to a deterioration in
measurement accuracy.
r Ensure that samples contain no insoluble
contaminants such as fibrin or dust.
Influence of vibrations
Incorrect results due to vibrations or Strong vibrations or knocking the instrument may
knocking the analyzer influence the positioning of the measuring devices and
lead to false results.
Strong vibrations or knocking the instrument may lead a
rack being moved to the rack entry position, which may
lead to incorrect sample identification.
r Ensure that no vibrations influence the surface the
analyzer stands on and take care not to knock the
analyzer while processing tests.
Incorrect results due to high ambient humidity Excessive ambient humidity may influence the chemical
reactions of test strips and lead to incorrect results.
r Always operate the analyzer in environmental
conditions defined in the technical specifications.
r Do not store test strip cassettes in their protective
packaging once the latter was opened.
r After removing them from their protective packaging,
always load the test strip cassettes in the test strip
cassette compartment within the time defined in their
Instructions for Use.
1 Safety
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
32 Safety summary
Malfunction of analyzer and incorrect results This analyzer has been designed and tested to CISPR 11
due to interfering electromagnetic fields Class A. In a domestic environment it may cause radio
interference, in which case, you may need to take
measures to mitigate the interference.
r The electromagnetic environment should be evaluated
prior to operation of the device.
r Do not operate this analyzer in close proximity to
sources of strong electromagnetic fields (for example
unshielded intentional RF sources), as these may
interfere with the proper operation.
Fatigue due to long hours of operation Looking at the monitor screen over an extended period of
time may lead to eye strain or body fatigue.
r Avoid spending long periods looking at the monitor
screen.
Notices
! List of notices
r Before operating, read the notices contained in this
summary carefully. Failure to observe them may result
in damage to equipment.
In this section
Moving parts (33)
Fuses (33)
Spillage (33)
Excessive ambient humidity (33)
Influence of vibrations (34)
1 Safety
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
Safety summary 33
Moving parts
Damage to the analyzer due to contact with Contact with moving parts may bend the sample probe or
moving parts damage some other component. If the analyzer detects a
collision, an alarm is issued and operation stops
immediately.
r Keep all covers closed and in place during operation.
r Do not touch any parts of the analyzer other than
those specified. Keep away from moving parts during
operation.
Fuses
Damage to the analyzer due to improper use r Should one of the fuses blow, do not attempt to
operate the analyzer before contacting your Roche
Service representative.
Spillage
Malfunction due to spilled liquid Any liquid spilled on the analyzer may result in
malfunction or damage.
r Do not place samples or any other liquid on the
surface of the analyzer.
r If liquid does spill on the analyzer, wipe it up
immediately and apply disinfectant. Be sure to wear
protective equipment.
Malfunction due to high ambient humidity Excessive ambient humidity may cause condensation
inside the analyzer and lead to short-circuiting in
electrical components.
r Always operate the analyzer in environmental
1 Safety
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
34 Safety labels on the equipment
Influence of vibrations
Analyzer malfunction due to sample spillage Strong vibrations or knocking the instrument may lead to
spillage of sample, which may lead to malfunction of the
analyzer.
r Ensure that no vibrations influence the surface the
analyzer stands on and take care not to knock the
analyzer while processing tests.
In this section
Analyzer views (34)
Analyzer views
In this section
Front view (35)
Back view (36)
Solid waste compartment (37)
1 Safety
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
Safety labels on the equipment 35
Front view
Safety labels on the test strip analyzer
(front view)
A D C
B
C
C
B
C
C
C
E
C C
C E
B ESD sensitivity
This label indicates a part that is electromagnetically sensitive.
Do not operate this analyzer in close proximity to sources of strong
electromagnetic fields (for example unshielded intentional RF sources), as these
may interfere with the proper operation.
C Moving parts
This label indicates that there is a danger of moving parts within the vicinity of
this label. Keep hands away from moving parts.
E Biohazard warning
This label indicates that there are potential biohazards within the vicinity of this
label.
The user is responsible for cleaning the area if biohazardous material was
spilled.
Follow Good Laboratory Practices for working with biohazardous materials.
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
36 Safety labels on the equipment
Back view
Safety labels at the rear of the test strip
analyzer
w Safety labels at the rear of the test strip analyzer (control unit version 1)
w Safety labels at the rear of the test strip analyzer (control unit version 2)
A Warning
This label indicates that there are hazardous situations arising within the vicinity
1 Safety
of this label, which may result in death or serious injury. Refer to the Operator’s
Manual for instructions on safe operation.
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
Safety labels on the equipment 37
A Biohazard warning
This label indicates that there are potential biohazards within the vicinity of this
label.
The user is responsible for cleaning the area if biohazardous material was
spilled.
Follow Good Laboratory Practices for working with biohazardous materials.
1 Safety
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
38 Safety labels on the equipment
A Electrical warning
Contact with electrical components can cause an electric shock. This label
indicates that there is a danger of coming into contact with electrical
components, when gaining access to parts of the system marked with this label.
Refer to the Operator’s Manual for instructions on safe operation.
A B
A Moving parts
This label indicates that there is a danger of moving parts within the vicinity of
this label. Keep hands away from moving parts.
B Biohazard warning
This label indicates that there are potential biohazards within the vicinity of this
label.
The user is responsible for cleaning the area if biohazardous material was
spilled.
Follow Good Laboratory Practices for working with biohazardous materials.
1 Safety
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
Disposal of the equipment 39
1 Safety
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
40
1 Safety Disposal of the equipment
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cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
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Table of contents
Introduction 2
In this chapter 2
General description . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 43
Introducing the analyzer . . . . . . . . . . . . . . . . . . . . . 45
Operator assistance . . . . . . . . . . . . . . . . . . . . . . . . . 46
Principles of operation . . . . . . . . . . . . . . . . . . . . . . . 47
Checking the analyzer status . . . . . . . . . . . . . . . . . 49
Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 50
Quality control (QC) . . . . . . . . . . . . . . . . . . . . . . . . . 50
Daily operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51
Short guide to a typical work session . . . . . . . . . . 51
Result handling . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 54
Viewing results . . . . . . . . . . . . . . . . . . . . . . . . . . 55
Validating results. . . . . . . . . . . . . . . . . . . . . . . . . 56
Printing and exporting results. . . . . . . . . . . . . . 56
End of shift . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57
Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 57
2 Introduction
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Table of contents
2 Introduction
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cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
General description 43
General description
In this section
Overview (43)
Introducing the analyzer (45)
Operator assistance (46)
Principles of operation (47)
Checking the analyzer status (49)
Calibration (50)
Quality control (QC) (50)
Overview
The cobas u 601 urine analyzer (called test strip analyzer
in this documentation) is a fully automated urine analysis
system intended for in vitro qualitative or semi-
quantitative determination of urine analytes.
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General description 45
F G H I
J
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46 General description
Operator assistance
The main tools for assisting with operation are wizards
that guide you through selected tasks, and the user
documentation.
w Assistance tab
2 Introduction
u Related topics
• Wizards (135)
• Online help (139)
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cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
General description 47
Principles of operation
The analyzer is basically designed to operate with rack
and sample barcodes, but you can use the system without
sample barcodes. Rack barcodes are used to identify the
various rack types; dedicated racks are used for
performing patient tests, QC tests, and wash actions of
the fluid system. This allows a high degree of automation,
whereby the tests and activities start automatically when
you load the corresponding rack.
2 Introduction
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cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
48 General description
(1) The minimal sample volume required depends on the test profile. See
Minimal sample volumes (dependent on test profile) (112)
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cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
General description 49
Task indicator
Color Meaning
Red The task requires immediate operator intervention. Operation may have stopped.
When such a task is generated, an acoustic signal is sounded as well, unless this
function is turned off.
Orange The task requires early operator intervention, operation may otherwise stop.
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50 General description
Task list The task list contains the task buttons. Choosing such a
button either leads to a list of all messages of the
category or to a panel that contains information and
functions related to the issue mentioned in the task
button (supplies, orders, results).
Calibration
In order to ensure proper functioning of the photometer
unit, a calibration needs to be performed every 4 weeks. It
consists of measuring the pads of a dedicated calibration
strip and of the built-in reference plate.
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Daily operation 51
Daily operation
In this section
Overview (51)
Short guide to a typical work session (51)
Result handling (54)
End of shift (57)
Maintenance (57)
Overview
Daily operation consists of the following phases:
1. Preparing the system
- Ensure that all consumables are available, the
water container is full, and the liquid waste
container is empty.
- Address the issues of all red or orange entries in
the task list.
2. Performing tests and ongoing maintenance
- Load the samples.
- Clean up spills, replenish consumables as needed.
- Validate the results.
- Print results and save as PDF files as required.
- Unload the samples.
3. Keeping the data safe
- Archive the results according to your laboratory
procedures.
4. Keeping the analyzer clean
- Empty the liquid and solid waste containers.
- Perform the daily wash action and shut down the
system.
- Clean the input and output buffers.
- Clean the rack conveyors.
- Clean the test strip tray, test strip transporter, and
the test strip pipetting area.
2 Introduction
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52 Daily operation
5 Loading the samples and o Ensure that the sample barcodes point towards
racks that long side of the rack where the rack barcode
is affixed.
o Ensure that the rack barcodes point outwards and
towards the back of the analyzer when placed on
the input buffer.
The analyzer detects the presence of the rack tray or
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Daily operation 53
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cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
54 Daily operation
12 Performing end of shift If the next shift does not follow immediately after,
maintenance and shutting perform the following tasks:
down the analyzer 1. Archive the results according to your laboratory
procedures, if required.
2. Empty the liquid and solid waste containers.
3. Perform the daily wash action and shut down the
system.
4. Clean the input and output buffers.
5. Clean the rack conveyors.
6. Clean the test strip tray, test strip transporter, and
the test strip pipetting area.
7. Clean the probe bend detector.
8. Remove spills and soiling from the analyzer
housing.
y Short guide for performing tests
Result handling
In this section
Overview (54)
Viewing results (55)
Validating results (56)
Printing and exporting results (56)
2 Introduction
Overview
You can set up the analyzer to automatically validate all
results or to exclude results from automatic validation if
they have certain data alarms associated with them. You
can also choose to validate all results manually.
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Daily operation 55
Viewing results
Results are displayed in a dedicated panel, and both full-
screen and split-screen displays are available. Exactly
which results are displayed can be defined with the help
of so-called views; for example you can display only
results that have not been validated yet. You can also
search for specific results or a group of results by
entering part of the sample ID in the Search field.
2 Introduction
w Result display
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56 Daily operation
Validating results
Value ranges and limits are used to determine whether a
result is positive or negative and whether to trigger data
alarms and actions such performing additional tests. If
these ranges and values are exceeded data alarms are
generated and the results are marked accordingly; these
indications help you identify critical results and point to
possible actions that need to be taken.
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Daily operation 57
End of shift
If the next shift does not follow immediately after, Roche
recommends to perform the following tasks:
1. Archive the results according to your laboratory
procedures.
2. Empty the liquid and solid waste containers.
3. Perform the daily wash action and shut down the
system.
4. Clean the input and output buffers.
5. Clean the rack conveyors.
6. Clean the test strip tray, test strip transporter, and the
test strip pipetting area.
7. Clean the probe bend detector.
8. Remove spills and soiling from the analyzer housing.
Maintenance
For routine operation, all maintenance actions can be
performed using wizards, which are sets of interactive
step-by-step instructions. You are informed by a message
in the message list when a maintenance action is due,
choosing such a message leads to detailed information
and to the appropriate wizard.
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2 Introduction Daily operation
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59
Table of contents
Hardware 3
In this chapter 3
Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 61
Main components. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 63
Covers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 64
Connectors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 66
About connectors . . . . . . . . . . . . . . . . . . . . . . . . . . . 66
Liquid connectors. . . . . . . . . . . . . . . . . . . . . . . . . . . 69
About liquid connectors . . . . . . . . . . . . . . . . . . 69
With external water supply . . . . . . . . . . . . . . . . 71
Power switches . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 72
Input and output buffers . . . . . . . . . . . . . . . . . . . . . . . . 74
Input buffer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 75
Output buffer. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 76
Input connection unit. . . . . . . . . . . . . . . . . . . . . . . . 76
Tubes, racks, and rack trays . . . . . . . . . . . . . . . . . . . . . 78
Tubes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 78
Racks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 79
Rack trays . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 81
3 Hardware
Liquid containers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 83
Water container. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 83
Water container for external water supply . . . . . . 84
Liquid waste container. . . . . . . . . . . . . . . . . . . . . . . 85
Liquid waste with external water supply . . . . . 86
Solid waste container. . . . . . . . . . . . . . . . . . . . . . . . . . . 87
Rack transport unit. . . . . . . . . . . . . . . . . . . . . . . . . . . . . 88
Fluid system. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 89
About the fluid system . . . . . . . . . . . . . . . . . . . . . . . 89
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Table of contents
Pipetting unit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 91
About the pipetting unit. . . . . . . . . . . . . . . . . . . 92
Probe calibration. . . . . . . . . . . . . . . . . . . . . . . . . 92
Rinse station . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 93
Sample handling. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 94
Test strip handling . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 95
About test strip handling . . . . . . . . . . . . . . . . . . . . . 95
Test strip cassette . . . . . . . . . . . . . . . . . . . . . . . . . . . 98
Test strip cassette compartment. . . . . . . . . . . . . . . 99
Test strip processing . . . . . . . . . . . . . . . . . . . . . . . . 101
Reflectance photometric measuring . . . . . . . . . . . 102
About reflectance photometric measuring . . . 102
Compensation measurement . . . . . . . . . . . . . . 103
Measuring cell . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 104
Barcode reader . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 105
Barcodes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 106
Radio frequency identification . . . . . . . . . . . . . . . . . . . 107
Technical specifications . . . . . . . . . . . . . . . . . . . . . . . . . 109
List of technical specifications . . . . . . . . . . . . . . . . 109
Storage conditions . . . . . . . . . . . . . . . . . . . . . . . 110
Environmental conditions . . . . . . . . . . . . . . . . . 110
Physical dimensions . . . . . . . . . . . . . . . . . . . . . . 110
Effective footprint . . . . . . . . . . . . . . . . . . . . . . . . 110
Allowed tilt. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 111
Power requirements . . . . . . . . . . . . . . . . . . . . . . 111
Uninterruptible power supply (UPS) . . . . . . . . 111
Heat output . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 111
Noise level . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 111
Measurement principles . . . . . . . . . . . . . . . . . . 112
Interfaces . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 112
Throughput . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 112
Minimal sample volumes (dependent on test
profile) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 112
Water quality . . . . . . . . . . . . . . . . . . . . . . . . . . . . 112
Wash solution . . . . . . . . . . . . . . . . . . . . . . . . . . . 113
Cleaning solutions . . . . . . . . . . . . . . . . . . . . . . . 113
Waste handling . . . . . . . . . . . . . . . . . . . . . . . . . . 113
Display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 113
Keyboard . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 114
Mouse . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 114
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Safety 61
Safety
! Read and understand the information in the
Safety chapter
! CAUTION
Personal injury and damage to the analyzer due to
improper handling
Touching the probe with bare fingers may leave residues
on its surface and consequently influence the accuracy of
the results.
The analyzer is quite heavy. Attempting to move it without
the appropriate resources, tools and techniques may lead
to personal injury and to damage to the analyzer by
dropping it from some height.
r Do not attempt to lift the analyzer by yourself.
r To move the analyzer, always use the resources, tools
and techniques in accordance with the regulations
that apply to you locally.
NOTICE
Malfunction due to inappropriate placing of the
analyzer
Placing the analyzer on an uneven or slanting surface
may impair its proper functioning.
Placing the analyzer on a surface that cannot be reached
comfortably by all operating personnel may lead to
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62 Safety
NOTICE
Malfunction due to incompatible monitor drivers
For proper functioning of the monitor, the appropriate
drivers must be installed.
r Do not replace the monitor yourself. If it needs
replacing, contact your Roche Service representative.
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Main components 63
Main components
The following illustration highlights the main components.
F G H I
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A
K
B
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64 Covers
Covers
All covers must be kept closed during processing. They
should only be opened when instructed to do so by on-
screen instructions or as part of maintenance and
troubleshooting activities.
! WARNING
Personal injury due to contact with moving parts
r Keep the main cover closed and in place while the
analyzer is operating.
r During operation and maintenance, proceed
according to the instructions contained in the
Operator’s Manual.
r Observe the safety labels on the equipment.
! CAUTION
Personal injury due to incorrect handling of the
main cover
If the main cover is not fully opened, it may fall back to its
closed position and possibly trap your fingers in the
process.
r Always open the main cover fully to its upright
position.
r When closing the main cover, be sure not to position
your hands or fingers on the side frame of the
analyzer.
! CAUTION
Loss of data and sample due to opening covers or
drawers
Opening the main cover during operation interrupts the
power supply to all units, processing stops immediately
and no status information can be stored. Incomplete tests
and other activities will have to be redone.
Opening a waste drawer interrupts the current measuring
activities. No results are generated for the tests that have
3 Hardware
been started.
r Do not open any cover while the analyzer is
performing some activity. Only do so in an emergency.
For information on how to recover from such a
situation, see the following topics:
u When you have accidentally pulled the waste drawer
during operation (311)
u Recovering from an irregular stop (308)
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Covers 65
w Covers
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66 Connectors
Connectors
In this section
About connectors (66)
Liquid connectors (69)
About connectors
At the rear of the analyzer, there are connectors for mains
electricity, liquids, and data.
! CAUTION
Damage to the analyzer due to connecting
inappropriate devices
Connecting external devices that are not intended to be
used with the analyzer may damage the analyzer or
impair its functioning.
r Only connect external devices to the analyzer that are
intended to be used with the analyzer and mentioned
in the Operator’s Manual.
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Connectors 67
I J K
A N
O
B
P
Q
C
D E F G H
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68 Connectors
I J K L M
A P
Q
B R
S
C T
U
D E F G H
NOTICE
Operating complications due to simultaneous use of
virtual keyboard and external keyboard
The system is designed to be operated using the touch
screen, but you can use the supplied external keyboard
instead.
Setting up the instrument to work with the virtual
keyboard and at the same time connecting the external
keyboard may lead to operating complications.
r Only work with either the virtual keyboard or the
3 Hardware
external keyboard.
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Connectors 69
A B
Liquid connectors
In this section
About liquid connectors (69)
With external water supply (71)
! CAUTION
Incorrect results due to air in the tubing
If liquid connectors are not properly connected, air may
enter the tubing and consequently incorrect amounts of
liquid may be aspirated and dispensed, which can lead to
incorrect results.
r Be sure to screw on all liquid connectors properly,
place the connectors square on when connecting
them.
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70 Connectors
F G H I J
A
B
D
E
K
F G H I J
A
B
D
E
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Connectors 71
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72 Power switches
Power switches
q The analyzer automatically adjusts to 100 to 240 V
and 50 to 60 Hz mains electricity.
A D
A D
C
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Power switches 73
! CAUTION
Loss of data and sample due to turning off the
analyzer using the on/off switch
Pressing the on/off switch for several seconds stops all
processing and shuts down the internal PC. No status
information can be stored. Incomplete tests and other
activities will have to be redone.
r Do not use the on/off switch to turn off the analyzer
except in an emergency, e.g. when the screen is
“frozen” and analyzer does not react to any user
action on-screen or otherwise.
u For information on recovering from such an emergency
situation, see To recover from a forced shutdown (309).
! CAUTION
Loss of data and sample and damage to equipment
due to switching off power
Switching off the power using the power switch stops all
processing and no status information can be stored.
Incomplete tests and other activities will have to be
redone. Equipment may be damaged.
r Do not switch off power during operation.
r Ensure that the mains cables are placed safely away
from areas where personnel might pass through.
r Roche recommends using an uninterruptible power
supply.
u Uninterruptible power supply (UPS) (111)
u For information on recovering from such an emergency
situation, see To recover from a power outage (312).
3 Hardware
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74 Input and output buffers
! CAUTION
Personal injury due to contact with moving parts
Racks are moved automatically on the input and output
buffers by the rack pusher. If you place your hands or
fingers on a buffer while racks are moved you may get
your fingers caught.
r Do not place your hands on the input or output buffer
or the racks while the analyzer moves racks.
r Do not load racks while the analyzer moves racks on
the input buffer.
r Do not unload racks while the analyzer moves racks
on the output buffer.
In this section
Input buffer (75)
Output buffer (76)
Input connection unit (76)
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Input and output buffers 75
Input buffer
The space is divided into the area for the input rack tray
with up to 15 racks, the single rack slot and the priority
rack slot.
A B
w Input buffer
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76 Input and output buffers
Output buffer
There is space for up to 15 racks on the output rack tray.
A message is generated in the message list when the
output rack tray is full. No new racks can be processed
when the rack is full.
w Output buffer
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Input and output buffers 77
! CAUTION
Incorrect results and damage to the analyzer due to
use of non-recommended type of rack
Using racks that do not conform to the established
dimensions may lead to malfunction or pipetting errors
and consequently to incorrect results.
Racks with unsuitable colors may lead to barcode reading
errors.
r Only use racks defined in the following table:
u Supported tube types for allowed rack types y (78)
NOTICE
Malfunction due to placing items on the ICU
r Do not place anything on the ICU.
r Always make sure that the rack conveyor belt of the
input connection unit is unobstructed.
B C
A Rack conveyor belt of the input connection unit C Input connection unit
B Connection line
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78 Tubes, racks, and rack trays
In this section
Tubes (78)
Racks (79)
Rack trays (81)
Tubes
The following table lists the supported tube types for the
allowed rack types.
Rack type Round bottom tube Conical bottom tube False bottom tube
ø 13 mm ø 16 mm ø 13-16 mm ø 13 mm ø 16 mm ø 13 mm ø 16 mm
Standard RD 5 rack l l l x l l l
(gray)
RD 5 wash rack (green) l l l x l x x
RD 5 QC rack (white) l l l x l l l
URISYS rack (yellow) x l x x l x x
y Supported tube types for allowed rack types
installation.
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Tubes, racks, and rack trays 79
! CAUTION
Malfunction or incorrect results due to using
inappropriate tubes
The analyzer has been designed and tested for the use of
specific types of tubes.
Using tubes that do not conform to the specified
dimensions and that are not defined for this analyzer may
lead to malfunction or pipetting errors and consequently
to incorrect results.
r Only use the tubes defined for this analyzer.
Racks
The analyzer is designed to handle the racks defined in
the following table:
u Tubes (78)
! CAUTION
Malfunction or incorrect results due to using
inappropriate racks
Using racks that do not conform to the established
dimensions may lead to malfunction or pipetting errors
and consequently to incorrect results.
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80 Tubes, racks, and rack trays
! CAUTION
Malfunction or incorrect results due to using
inappropriate rack rubber disks
Using rack rubber disks that differ in height from the
original ones may lead to malfunction or pipetting errors
and consequently to incorrect results.
r Do not replace individual rack rubber disks, if one is
damaged, replace the whole rack.
A B
B
Sample rack All racks that are not specifically defined as STAT racks,
wash racks, or QC racks are treated as sample racks.
STAT rack The STAT rack is a dedicated sample rack for performing
STAT tests.
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Tubes, racks, and rack trays 81
Wash rack The wash rack is a dedicated rack for performing the
daily wash maintenance action. It contains the required
wash solution.
u For information on how to define a wash rack and how
to assign it to the analyzer, see Managing racks (276).
Rack trays
A rack tray can hold up to 15 racks. Generally, racks are
loaded onto rack trays for loading on and unloading from
the analyzer. For processing single racks there is a priority
rack slot and a single rack slot.
3 Hardware
You can load one rack tray on the input buffer and one
on the output buffer. The analyzer monitors the fill level of
the output buffer and whether there is a rack tray or
individual racks on the input buffer.
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82 Tubes, racks, and rack trays
NOTICE
Malfunction due to damaged rack tray
A rack tray that is dented or bent or damaged in any other
way may impede the locking mechanism.
r Be sure to use undamaged rack trays only.
NOTICE
Malfunction due to unsupported rack trays
Using unsupported rack trays can cause the analyzer to
block or the sensor to malfunction.
r Only use supported rack trays.
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Liquid containers 83
Liquid containers
The water containers and the liquid waste containers are
positioned under the table on which the analyzer is
placed. Their fill levels are monitored and messages in the
message list inform you when certain levels have been
reached or when a container is full or empty.
In this section
Water container (83)
Water container for external water supply (84)
Liquid waste container (85)
Water container
The white water containers hold up to 5 L of water.
C
D
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84 Liquid containers
! CAUTION
Incorrect results due to incorrect water pressure in
the external water supply
Working with incorrect water pressure may lead to
hardware malfunction and consequently insufficient or
irregular water supply to the analyzer and possibly air
bubbles in the fluid system.
r The water pressure at the water inlet on the water
container must not exceed 4 bar.
r Use water of the specified quality:
u Water quality (112)
! CAUTION
Contamination due to deposits of algae and bacteria
In the inside of the bottle where it is exposed to air,
deposits of algae and bacteria may build up over time.
r Clean the water container once a month.
u To clean the water container for external water
supply (288)
! CAUTION
Overfilling of the water container when the analyzer
is switched off
When the analyzer is switched off, the water level sensors
do not work and consequently cannot warn the operator
if the water container accidentally becomes too full.
r Turn off the external water supply when you switch off
the analyzer.
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Liquid containers 85
! CAUTION
Infection by liquid waste
Contact with liquid waste may result in infection. All
materials and mechanical components associated with
the waste systems are potentially biohazardous.
r Be sure to wear protective equipment. Take extra care
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86 Liquid containers
! CAUTION
Spilling and infection by liquid waste
If you work with external water supply, the waste outlets
are directly connected to the laboratory waste system,
and no liquid waste container is required. Connecting the
liquid waste container could lead to overflow of the liquid
waste container, because the liquid level sensors are
disabled.
r Never install the liquid waste container if you work
with external water supply.
! CAUTION
Incorrect results due to inefficient wash actions
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Solid waste container 87
NOTICE
Analyzer damage due to overfilled solid waste
container
If the solid waste container is full, test strips may get
stuck in the waste chute or the test strip tray and the may
interfere with the measuring mechanism.
r Be sure to empty the solid waste container when you
are alerted by a message in the task list.
r Roche recommends emptying the solid waste
container whenever you load a new test strip cassette.
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88 Rack transport unit
A F
B C
position.
All samples on the rack are pipetted.
4. When all tubes on the rack are processed, the rack
conveyor moves the rack to the rack exit position on
the output buffer.
5. The rack pusher moves the rack onto the rack tray on
the output buffer.
6. The operator removes the rack, either by itself or by
removing the rack tray.
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Fluid system 89
Fluid system
In this section
About the fluid system (89)
Pipetting unit (91)
Rinse station (93)
A
G
B
H
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A Transfer head E Water level sensor connector and liquid waste level sensor
connector at the back of the analyzer
B Measuring cell F External liquid connectors at the back of the analyzer
C Pipetting unit with probe G Peristaltic pumps
D Rinse station H Syringes
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90 Fluid system
A
G
B
A Transfer head E Water level sensor connector and liquid waste level sensor
connector at the back of the analyzer
B Measuring cell F External liquid connectors at the back of the analyzer
C Pipetting unit with probe G Peristaltic pumps
D Rinse station H Syringes
Pipetting unit The pipetting unit moves the probe to the appropriate
positions for aspirating and dispensing liquid. It is
equipped with liquid detection and probe crash
prevention mechanisms.
u Pipetting unit (91)
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Fluid system 91
! WARNING
Incorrect results due to touching the probe
Touching the probe with bare fingers may leave residues
on its surface and consequently influence the accuracy of
the results.
r Do not touch the probe except for maintenance as
described on screen or in this documentation.
Rinse station The rinse station serves to clean the probe after each
pipetting action to prevent carryover between samples.
u Rinse station (93)
Fluid system The fluid system with its syringes and pumps controls the
aspiration and dispensing of sample. It also controls the
supply of system water and wash solution. The probe is
rinsed with system water after every pipetting action to
prevent carryover between samples.
External liquid connectors There is a water and two waste connections, one of them
being a safety outlet for cases when the tubing of the
main connection is blocked.
Pipetting unit
In this section
About the pipetting unit (92)
Probe calibration (92)
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92 Fluid system
Probe calibration
During initialization of the analyzer the probe positioning
is automatically calibrated and its position adjusted. This
is done by moving the probe in the horizontal and vertical
plane along a reference block.
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Fluid system 93
Rinse station
The probe is rinsed after each pipetting. It is lowered in
the probe chamber of the rinse station and then water is
pumped through the probe to wash it in and outside.
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94 Sample handling
Sample handling
Before urine is pipetted, it is mixed to ensure even
distribution of particles. This process is performed by
aspirating and dispensing urine in the sample tube on the
sampling position.
H
B
I
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C D E
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Test strip handling 95
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96 Test strip handling
B C D E
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Test strip handling 97
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98 Test strip handling
A Groove
A Hook
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Test strip handling 99
NOTICE
Diminished test strip stability due to excessive
ambient humidity
Excessive ambient humidity will limit the effectiveness of
the desiccant in the test strip cassette and may render the
test strips unsuitable for use.
r Use the analyzer only in the environmental conditions
defined in:
u Environmental conditions (110)
r Open this compartment only for replacing the test
strip cassette.
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100 Test strip handling
! CAUTION
Incorrect results due to excessive ambient humidity
Excessive ambient humidity will limit the effectiveness of
the desiccant in the test strip cassette and consequently
may influence the test pad constituents in a manner that
incorrect results are generated.
r Use the analyzer only in the environmental conditions
defined in:
u Environmental conditions (110)
r Always load the test strip cassette immediately after
removing it from its airtight packaging. Follow the
instructions defined in the cobas u pack Method
Sheet.
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Test strip handling 101
B C D E
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102 Test strip handling
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Test strip handling 103
C D C
w Schematic of photometer
Compensation measurement
Intrinsic coloring of the urine influences the reflectance
value and may lead to false results. For this reason, a
white reagent-free compensation pad is measured to
establish a correction algorithm. When calculating the
measurement results of the test pads, this algorithm is
used to compensate for the intrinsic urine coloring.
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104 Test strip handling
Measuring cell
The measuring cell establishes the specific gravity and
clarity of the sample. Sample is passed through a
transparent tube in the measuring cell, where a
refractometer determines the specific gravity and the
turbidimeter determines the clarity. Specific gravity and
clarity are not affected by the intrinsic color of the urine.
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Barcode reader 105
Barcode reader
Barcode readers using LED technology with very low
output power are used to scan the barcodes on samples
and racks.
! WARNING
Loss of sight
The intense light of the LEDs may damage your eyes.
r Do not stare into the LEDs.
w Barcode reader
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106 Barcodes
Barcodes
Barcodes are used on racks and sample tubes. The
minimum resolution of a barcode line is 0.2 mm and the
maximum barcode length is 72 mm. The barcode must be
at least 35 mm away from the bottom of the rack.
A Barcode line resolution min. 0.2 mm C Distance from rack bottom min. 35 mm
B Barcode length max. 72 mm
! WARNING
Unidentified samples due to undetected reading
errors
Barcode reading errors could potentially go undetected if
a checksum is not used, which could lead to sample
mismatch.
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Radio frequency identification 107
A RFID reader for QC materials B RFID reader for test strip cassette
w RFID readers
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108 Radio frequency identification
QC material o QC level
o Target ranges
o Lot number
o Expiry date
y RFID tag information
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Technical specifications 109
Technical specifications
q Technical specifications may change without
notice
Every effort has been made to ensure that all the
information contained in these specifications is correct at
the time of publication. However, Roche reserves the right
to make any changes necessary without notice as part of
ongoing product development.
In this section
List of technical specifications (109)
Standard supplies (114)
Optional components (114)
Concentration ranges (International) (115)
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110 Technical specifications
Storage conditions
Environmental conditions
Physical dimensions
Effective footprint
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Technical specifications 111
Allowed tilt
Incline < 3º
y Allowed tilt
Power requirements
Heat output
y Heat output
Noise level
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112 Technical specifications
Measurement principles
Reflectance photometry
Refractometry
Turbidimetry
y Measurement principles
Interfaces
Throughput
Water quality
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Technical specifications 113
Wash solution
Cleaning solutions
Waste handling
Solid waste container for test strips Capacity: 400 test strips
Inside dimensions: (W x D x H): 8.34 cm x 13.34 cm x 11.82 cm (3.28 in x 5.25 in
x 4.65 in)
Liquid waste container Capacity: 5 L
Dimensions: (diameter x H): 16.2 cm x 32.5 cm (6.38 in x 12.80 in)
Water container Capacity: 5 L
Dimensions: (diameter x H): 16.2 cm x 33.5 cm (6.38 in x 13.19 in)
Water container for external water supply Capacity: 5 L
Dimensions: (diameter x H): 16.2 cm x 32.5 cm (6.38 in x 12.80 in)
y Waste handling
Display
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114 Technical specifications
Keyboard
Mouse
Standard supplies
The analyzer has been tested for the following Roche
supplies:
• cobas u pack
• cobas u calibration strip
Optional components
The following optional components are available:
• cobas® 6500 installation kit for LAS
• Colored labels for Roche 5-position racks:
- Label for Std-rack, color yellow
- Label for Std-rack, color light blue
- Label for Std-rack, color dark blue
- Label for Std-rack, color light green
- Label for Std-rack, color orange
- Label for Std-rack, color pink
- Label for Std-rack, color brown
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Technical specifications 115
150/μL 150/μL 4+
250/μL 250/μL 5+
COL p. yel. p. yel. p. yel.
yellow yellow yellow
amber amber amber
brown brown brown
orange orange orange
red red red
green green green
other other other
y International concentration ranges for the cobas u 601 urine analyzer
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116
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117
Table of contents
Software 4
In this chapter 4
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 119
Key screen elements . . . . . . . . . . . . . . . . . . . . . . . . . . . 119
Key work areas . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 125
Tabs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 127
Displaying information . . . . . . . . . . . . . . . . . . . . . . . . . . 129
About displaying information . . . . . . . . . . . . . . . . . 129
Working with lists (tables) . . . . . . . . . . . . . . . . . . . . . . . 130
About sorting lists. . . . . . . . . . . . . . . . . . . . . . . . . . . 130
About filtering table information . . . . . . . . . . . . . . 130
About selecting table items. . . . . . . . . . . . . . . . . . . 130
Entering information. . . . . . . . . . . . . . . . . . . . . . . . . . . . 131
Working with QC charts. . . . . . . . . . . . . . . . . . . . . . . . . 133
External keyboard and mouse . . . . . . . . . . . . . . . . . . . 134
Wizards . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 135
About wizards . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 135
Examples . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 135
Example: Starting a wizard . . . . . . . . . . . . . . . . 136
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Table of contents
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Introduction 119
Introduction
q Throughout this documentation, images of screens
are included for illustration purposes. They are not
necessarily identical with what you see on your analyzer.
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120 Key screen elements
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Key screen elements 121
A
H
I
E
F G
D Tabs representing work areas I Routine tab in split-screen mode display (two panels)
E Navigation bar with back and forward buttons and
navigation path
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122 Key screen elements
A B C D E F G H I
Color Meaning
Red The task requires immediate operator intervention. Operation may have stopped.
When such a task is generated, an acoustic signal is sounded as well, unless this
function is turned off.
Orange The task requires early operator intervention, operation may otherwise stop. When
such a task is generated, an acoustic signal is sounded as well, unless this function
is turned off.
Gray Ongoing task. If operator intervention is required, perform it.
Task list, message list, and buttons Use the task buttons to display a list of all messages of a
given category and severity (message list). Choose a
message to display details of the message. These could
for example contain a button for starting a wizard that
guides you through the various steps of dealing with the
issue.
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Key screen elements 123
C D E
Tabs
Navigation bar
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124 Key screen elements
Assistance
Callouts
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Key work areas 125
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126 Key work areas
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Tabs 127
Tabs
When choosing a tab, a list is displayed with the buttons
for the items dealt with in this work area (A). Choosing
one of these buttons displays two panels next to each
other (B); the panel on the left (the main panel) usually
contains a list whose elements can be selected. It may
also contain buttons for starting tasks and features for
preselecting the type of information that should be
contained in the list. The panel on the right (the detail
panel) contains information related to the item selected in
the left panel, and it may also contain buttons.
4 Software
Display modes Another feature of some tabs is the fact that they can be
displayed in either full-screen or split-screen mode.
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128 Tabs
1 2 1
1 1 2
1 2 2
2 1 2
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Displaying information 129
Displaying information
In this section
About displaying information (129)
B Tabs D Panels
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130 Working with lists (tables)
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Entering information 131
Entering information
Normally the virtual keyboard is displayed whenever you
need to enter information. (The system is designed to be
operated using the touch screen, but you can use the
supplied external keyboard and mouse instead. If you do
so ensure that the virtual keyboard is not displayed
(Administration > Basic configuration 2)).
A Close the keyboard callout B Go to the next input field or to the next tab
q Keyboard layout
The virtual keyboard layout corresponds to the US English
QWERTY keyboard layout. This cannot be changed.
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132 Entering information
A B
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Working with QC charts 133
Choose this button to move back the displayed time interval by one month.
To continuously move back the displayed time interval, keep the button pressed.
Use this button to move forward the displayed time interval by one month.
To continuously move forward the displayed time interval, keep the button pressed.
Use this button to double the size of the displayed items, i.e. to increase the scale.
You can increase the scale four times.
Use this button to half the size of the displayed items, i.e. to decrease the scale.
You can decrease the scale until normal view is displayed (100%).
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134 External keyboard and mouse
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Wizards 135
Wizards
In this section
About wizards (135)
Examples (135)
About wizards
A wizard is an interactive set of step-by-step instructions
for performing a certain task. The instructions that are
currently displayed depend on checks the analyzer
performs continuously and on user input, for example a
confirmation that a certain step has been completed or
on entering data.
Examples
In this section
Example: Starting a wizard (136)
Example: Using a wizard for performing a task that is
due (136)
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136 Wizards
r To start a wizard
2
2 Choose the button for the task you want to perform,
for example for filling the water container.
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Wizards 137
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138 Color coding
Color coding
The color of buttons and other display items inform you
about the status of the display item or the item it
represents.
Color Meaning
Light gray You cannot currently select this element.
Red Pathological.
Color Meaning
Yellow For this sample, the SG parameter could not be measured in the measuring cell.
4 Software
Red No result could be generated by the measuring cell for the SG parameter. (Instead of a
result, "–" is displayed.)
y Color concept for severity of measurement errors in the measuring cell
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Online help 139
Online help
The analyzer provides online user information and
assistance, which can be accessed in the following ways:
A
E
B
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140 Online help
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Operation
5 Operation.................................................................................................................143
6 Configuration .........................................................................................................241
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Table of contents
Operation 5
In this chapter 5
Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 147
Short guide to routine testing . . . . . . . . . . . . . . . . . . . . 149
Routine operating tasks. . . . . . . . . . . . . . . . . . . . . . . . . 152
Starting the analyzer . . . . . . . . . . . . . . . . . . . . . . . . 152
Logging on . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 153
Preparing the analyzer . . . . . . . . . . . . . . . . . . . . . . . 154
Managing sample sequence numbers . . . . . . . . . 155
Defining the sample sequence number
ranges . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 156
Defining the next sample sequence number
to be used . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 157
Defining orders . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 157
Defining orders . . . . . . . . . . . . . . . . . . . . . . . . . . 158
Defining an order manually when working
with Sample sequence number mode . . . . . . . 159
Loading racks . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 160
About loading racks . . . . . . . . . . . . . . . . . . . . . . 160
Priority racks . . . . . . . . . . . . . . . . . . . . . . . . . . . . 163
Starting the testing process . . . . . . . . . . . . . . . . . . 165
Starting sample testing . . . . . . . . . . . . . . . . . . . 165
5 Operation
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Table of contents
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Table of contents
5 Operation
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Table of contents
5 Operation
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Safety 147
Safety
! Read and understand the information in the
Safety chapter
Warning messages:
u Biohazardous materials (27)
u Waste (27)
Caution messages:
u Mechanical safety (30)
u Working solutions (30)
u Influence of vibrations (31)
Notice messages:
u Spillage (33)
u Excessive ambient humidity (33)
! CAUTION
Incorrect results due to extreme ambient
temperatures
High ambient temperatures may cause sample
evaporation during incubation of the test strip, which may
lead to incorrect results.
Low ambient temperatures may slow the chemical
reactions on the test strips, which may lead to incorrect
results.
r Always operate the analyzer in the specified ambient
conditions:
u Environmental conditions (110)
! CAUTION
Incorrect results due to contaminated samples
Solid particles in the sample may influence the
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148 Safety
! CAUTION
Incorrect results due to carryover of samples
Hands that are contaminated with urine can transfer
urine to the touch screen monitor or mouse, from where it
may be transferred to samples, leading to carryover.
r Avoid getting into contact with urine.
r If you get into contact with urine, either dispose of the
lab gloves immediately or clean them using one of the
recommended cleaning solutions.
! CAUTION
Incorrect results due to foamy and contaminated
samples
Foam in samples may lead to incorrect amounts of liquid
being aspirated and dispensed, which can lead to
incorrect results.
Insoluble contaminants in samples may cause clogging or
pipetting volume shortage and lead to deterioration in
measurement accuracy.
r Ensure that samples are clear of foam and insoluble
contaminants such as fibrin or dust.
! CAUTION
Loss of data and analyzer damage due to
disconnection of mains power
Disconnecting the mains cable while the analyzer is
processing may lead to loss of data and hardware
damage.
r Do not disconnect the mains cable while the analyzer
has not been shut down properly.
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Short guide to routine testing 149
5 Loading the samples and o Ensure that the sample barcodes point towards
racks that long side of the rack where the rack barcode
is affixed.
o Ensure that the rack barcodes point outwards and
towards the back of the analyzer when placed on
the input buffer.
The analyzer detects the presence of the rack tray or
of individual racks in the priority and single rack slots
and moves a rack onto the rack conveyor.
(If you work with an input connection unit, you do not
need to load racks manually, it is done automatically.)
y Short guide for performing tests
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7 Monitoring the analyzer 1. On the Overview work area, check the task
indicator and the task list.
Address all red or orange items in the task list.
2. Choose a task button.
If the message list is displayed, choose a
message, check the details, and follow the on-
screen instructions.
If another panel is displayed, for example the
supplies panel, perform the appropriate task,
usually a wizard is available.
Red: Issues that require immediate operator
intervention.
Orange: Issues that require early operator
intervention, operation may otherwise stop.
Gray: Messages that inform about the status of
ongoing tasks. If operator intervention is required,
perform it.
Light gray: There are no issues of the associated
severity.
The number in a button tells you how many
messages of this severity there are.
8 Validating the results 1. Choose Routine > Manage test results, if
required.
2. Select a result in the list and check for data
alarms and the range graphics.
Green: negative
Yellow: positive (low pathological)
Red: positive (pathological)
If you work with patient demographics you can
assign a patient to each result. Choose the No
patient assigned button.
3. Choose the Validate or Rerun button as
required.
You can set up the analyzer to automatically
accept all results or to exclude results from
automatic validation if they have certain data
alarms associated with them. You can also choose
to validate all results manually.
9 Printing or exporting To print selected or all results, choose Routine
selected or all results > Manage test results.
5 Operation
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Short guide to routine testing 151
12 Performing end of shift If the next shift does not follow immediately after,
maintenance and shutting perform the following tasks:
down the analyzer 1. Archive the results according to your laboratory
procedures, if required.
2. Empty the liquid and solid waste containers.
3. Perform the daily wash action and shut down the
system.
4. Clean the input and output buffers.
5. Clean the rack conveyors.
6. Clean the test strip tray, test strip transporter, and
the test strip pipetting area.
7. Clean the probe bend detector.
8. Remove spills and soiling from the analyzer
housing.
y Short guide for performing tests
5 Operation
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152 Routine operating tasks
In this section
Starting the analyzer (152)
Logging on (153)
Preparing the analyzer (154)
Managing sample sequence numbers (155)
Defining orders (157)
Loading racks (160)
Starting the testing process (165)
Checking the status of processing (167)
1
1 Power on the analyzer.
5 Operation
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Routine operating tasks 153
2
2 The analyzer software starts automatically. Performing
all the initialization and check procedures can take a
few minutes. During this process the Overview work
area is displayed.
Logging on
Results are always associated with the name of the
person who operated the analyzer at the time when the
test was performed. (This may be a legal requirement for
storing results.) Therefore, an operator must be logged on
to perform tests.
r To log on
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154 Routine operating tasks
1
1 On the Overview work area, check that there are no
red or orange buttons in the task list.
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u Related topics
• Defining the sample sequence number ranges (156)
In this section
Defining the sample sequence number ranges (156)
Defining the next sample sequence number to be
used (157)
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Routine operating tasks 157
Defining orders
5 Operation
In this section
Defining orders (158)
Defining an order manually when working with Sample
sequence number mode (159)
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158 Routine operating tasks
Defining orders
The system is basically designed to operate with rack and
sample barcodes. The orders are generated automatically
on the basis of the barcode information.
When working with Sample sequence number If you work with Sample sequence number mode, the
mode number is assigned when the tube is on the
measurement position.
! WARNING
Incorrect results due to sample mismatch when
working without sample barcodes
When working with Sample sequence number mode, it
is up to the operating staff to ensure that the sample
placement on the racks matches the definitions in the
orders.
If the rack number, rack position and sample ID of the
order do not agree with the actual racks and positions,
the results may not be associated with the correct patient
by the medical personnel.
r When working without sample barcodes, be sure to
load the samples according to the definitions in the
orders.
r Avoid empty positions within the racks. Do not place
non-registered samples in any empty rack position.
r When manually assigning rack positions, ensure the
5 Operation
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160 Routine operating tasks
u Related topics
• Managing patients (190)
Loading racks
In this section
About loading racks (160)
Priority racks (163)
! CAUTION
Personal injury due to contact with moving parts
Racks are moved automatically on the input buffer by the
rack pusher. If you place your hands or fingers on the
buffer while racks are moved you may get your fingers
caught.
r Do not place your hands on the input buffer or the
racks while testing is in progress.
NOTICE
Impaired tube content level detection due to metal
objects on tubes
Metal objects attached to tubes can impair the
5 Operation
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Routine operating tasks 161
NOTICE
Stand-alone operation
Malfunction and analyzer damage due to
obstructions
Placing objects on the rack tray or the input buffer may
cause rack jamming and malfunction when moving the
racks.
Placing racks or a rack tray on the input buffer when the
rack pusher is not in its resting position may cause rack
jamming and malfunction.
r Ensure that the rack trays and the input buffer are
always free of any foreign objects.
r Do not load racks or rack trays when the rack pusher
is not in its resting position.
A B C D
• You can place a single rack on the single rack slot (C).
• You can place a single rack on the priority rack slot
(A).
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162 Routine operating tasks
w Samples on a rack
Operation with input connection unit The racks are automatically fed onto the rack conveyor
belt of the input connection unit (A) by the rack conveyor
belt on the connection line (B).
A Rack conveyor belt of the input connection unit B Rack conveyor belt of the connection line
u Related topics
• Racks (79)
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Priority racks
Any rack that is placed on the priority rack slot is treated
as a priority rack.
Ensure that the rack barcode faces you and that sample
barcodes point towards that long side of the rack where
the rack barcode is affixed.
! WARNING
Incorrect results due to sample mismatch when
loading samples on the wrong rack
If you work with Sample sequence number mode and
place a STAT sample on a routine rack, the next routine
sample sequence number is assigned to this STAT
sample and the sample is processed as a routine sample
and not a STAT sample. Equally, if you place a routine
sample on a STAT rack, the next STAT sample sequence
number is assigned to this routine sample and the sample
is processed as a STAT sample and not a routine sample.
r Make sure you place every sample on the appropriate
rack.
NOTICE
Stand-alone operation
Malfunction and analyzer damage due to
inappropriate rack loading
Loading a rack on the priority rack slot while the rack
conveyor belt of this slot is moving or when the rack
pusher is not in its resting position may cause
malfunction of the instrument.
r Do not load a rack on the priority rack slot while the
rack conveyor belt is moving.
r Do not load a rack on the priority rack slot if the rack
pusher is not in its resting position.
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Operation with input connection unit Priority racks are loaded on the rack conveyor belt of the
input connection unit (A).
B
5 Operation
A Rack conveyor belt of the input connection unit B Rack conveyor belt of the connection line
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! CAUTION
Sample mismatch due to pending sample orders
Having pending sample orders in the order list may lead
to sample mismatch.
r Delete any pending sample orders from the order list
before starting the measurement.
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! CAUTION
Personal injury due to contact with moving parts
Racks are moved automatically on the input buffer by the
rack pusher. If you place your hands or fingers on the
input buffer while racks are moved you may get your
fingers caught.
r Do not place your hands on the input buffer or the
racks while the analyzer moves racks.
r Do not load racks while the analyzer moves racks on
the input buffer.
NOTICE
Malfunction and analyzer damage due to
inappropriate rack loading
Loading a rack on the priority rack slot while the rack
conveyor belt of this slot is moving or when the rack
pusher is not in its resting position may cause
malfunction of the instrument.
r Do not load a rack on the priority rack slot while the
rack conveyor belt is moving.
r Do not load a rack on the priority rack slot if the rack
pusher is not in its resting position.
1 Place the rack on the priority rack slot. Ensure that the
barcodes face towards the back of the analyzer.
f Processing starts automatically.
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Validated.
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170 Routine operating tasks
3
3 Display the complete orders list and check the status
indicators.
4
4 If there are errors:
• Choose the entry in the main panel.
• Choose the Status field in the detail panel.
f The message details are displayed.
5 Operation
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Result handling 171
Result handling
! CAUTION
Data loss due to failure of performing regular data
backup
The analyzer has limited storage space for results (for up
to 10 000 test results, depending on the system setup,
and for 300 each for QC, photometer calibration, and
measuring cell calibration.
Depending on the analyzer setup, when these limits are
reached, the oldest results may automatically be
overwritten or testing may stop.
r Periodically back up the database to an external
storage device and export the results.
In this section
Viewing results (171)
Validating results (172)
Managing invalid SG results (176)
Assigning patients (178)
Generating reports (179)
Viewing results
Results are displayed in a dedicated panel, both overview
and detail displays are available. Exactly which results are
displayed can be defined with the help of so-called views
or the text filter.
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172 Result handling
Validating results
All results need to be validated, the analyzer provides
several aids for doing so:
• You can set up the analyzer to automatically accept all
results or to exclude results from automatic validation
if they have certain data alarms associated with them.
You can also choose to validate all results manually.
u Defining the validation method (250)
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Result handling 173
Progress statuses
The order is being processed.
Validated.
Data alarms
No data alarm was generated.
A Abnormal result.
S Sieve result.
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174 Result handling
r To validate a result
2
2 From the Views drop-down list, choose Unvalidated
results.
f All results that have not been validate are listed.
f If your analyzer is connected to a LIS, all validated
results are automatically sent to the host computer
and would not be displayed in the result list.
f Results for which a data alarm was generated are
marked with in the column.
f In the column, the progress status is indicated.
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4
4 In the main panel, check for entries with a symbol
and choose one.
I The results are displayed in the detail panel.
5
5 Observe the status information in the detail panel.
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11
11 To validate the result, choose the Validate button.
f Accepted (validated) results are marked with in
the status column in the result list.
results.
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3
3 In the main panel, choose the entry of a sample with
an invalid SG, it is marked yellow .
5
5 In the detail panel, note the rack ID and sample
position.
f You can now measure SG for this sample
manually.
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4
4 In the main panel, choose the entry of the sample
whose SG you just have measured.
6
6 In the detail panel of the result details screen, choose
the Edit button.
Assigning patients
You typically use patient demographics if you want to
generate a patient report for the physician.
u Managing patients (190)
u Generating reports (179)
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Result handling 179
Generating reports
You can print selected results or save them to a file in
PDF format. You can also export the results in the
character separated values (CSV) data format for
reporting purposes or for processing in a spreadsheet
program.
u To export all results (289)
Result report To print or save to file results of certain samples, you can
filter and select results in the result list.
u To print results (result report) (180)
To save results to files (result report) (180)
Patient report To print or save to file results of certain patients, you can
select the patients in the patient list and then choose
which results of these patients you want to report.
u To print results (patient report) (180)
To save results to files (patient report) (181)
reports (270)
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Result handling 181
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182 Result handling
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Non-routine situations 183
Non-routine situations
The examination of the results and the messages in the
message list may point to one of the following situations.
o If the test that was performed does not u Rerunning tests (184)
agree with the one defined in the LIS
order, rerun the test.
If a questionable result was generated: u Rerunning tests (184)
o Rerun the test using the Rerun
function.
If no result was generated: u Rerunning tests when working with
o Adjust the order information and reload sample barcodes (184)
the sample.
o Make sure you are using a type of rack u Adjusting sample information (188)
that is recommended by Roche. u Tubes (78)
Rack barcode could not be read 1. Remove the rack from the output buffer.
2. Check the barcode for soiling, clean it.
If you could clean it, reload the rack.
3. If the barcode looks damaged, transfer
the tubes to another rack and load the
new rack.
y Exceptional processing situations
5 Operation
In this section
Rerunning tests (184)
Adjusting sample information (188)
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184 Non-routine situations
Rerunning tests
You would typically rerun a test if no result could be
generated or if you want to retest the sample with a
different test profile.
In this section
Rerunning tests when working with sample
barcodes (184)
Rerunning tests when working with Sample sequence
number mode (185)
Situation before rerun What you need to do What the analyzer does
The test has yielded a result. o Choose Routine > Manage test
results.
o From the result list, choose the result.
o Choose the Rerun button. A callout is displayed
o In the callout, choose the test profile, The new order is added to the orders list.
then choose the Create order button
o Place the sample tube on a rack, then The test is performed.
load the rack.
The test has not yielded a result. o Check the message in the message list. A message alerts you of the fact that no
result was generated.
The order is still on the analyzer.
o Choose Routine > Manage sample
order.
5 Operation
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Situation before rerun What you need to do What the analyzer does
The sample yielded results and the o Make a note of the sample IDs of the The orders are no longer available in the
results are already validated samples you want to rerun. orders list.
o Choose Routine > Manage test
results.
o Delete the results of the samples you
want to rerun.
o Place the sample on the rack, then load The test is performed.
the rack.
If you want to change the test profile:
o Make a note of the sample IDs of the The orders are no longer available in the
samples you want to rerun. orders list.
o Choose Routine > Manage sample
orders.
o Choose the Create button.
o Enter the original sample ID.
o Choose the test profile, if required.
o Assign the patient, if required.
o Choose the Save button. The new order is created.
o Place the sample on the rack, then load The test is performed.
the rack.
y Rerunning tests when working with sample barcodes
Situation before rerun What you need to do What the analyzer does
The sample does not have a o Make a note of the sample IDs of the The orders are no longer available in the
barcode label, the test has yielded a samples you want to rerun. orders list.
result and the result has been o Choose Routine > Manage test
validated. results.
o Delete the results of the samples you
want to rerun.
o Choose Routine > Manage sample
order.
o Choose the Create button.
o Enter the original sample ID.
o Enter the rack ID.
o Enter the rack position.
o Choose the test profile, if required.
o Assign a patient, if required.
o Choose the Save button. A new order is created.
o Be sure to place the sample on the rack The test is performed.
and position as defined above, then
5 Operation
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Situation before rerun What you need to do What the analyzer does
The test has yielded a result (not o Choose Routine > Manage test
validated) results.
o Select the result in question.
(You can select more than one result.)
o Choose the Rerun button. A callout is displayed.
o In the callout, choose the test profile, A new order is created.
then choose the Create order button. (If you selected more than one result, a new
order is created for each of them.)
o Choose Routine > Manage sample
orders.
o Select the order that was just created.
o In the detail panel, choose the Edit The original sample ID and the current date
button. and time are contained in the form.
(You cannot change this ID if you work with
Sample sequence number mode.)
o Enter the rack ID.
o Enter the rack position.
o Assign the patient, if required.
o Choose the Save button. The new order is created.
o Be sure to place the sample on the rack The test is performed.
and position as defined above, then
load the rack.
The test has not yielded a result o Choose Routine > Manage sample The order remains in the orders list.
orders.
o In the detail panel, choose the Edit The original sample ID and the current date
button. and time are contained in the form.
(You cannot change this ID if you work with
Sample sequence number mode.)
o Enter the rack ID.
o Enter the rack position.
o Choose the test profile, if required.
o Assign the patient, if required.
o Choose the Save button. The new order is created.
o Be sure to place the sample on the rack The test is performed.
and position as defined above, then
load the rack.
y Rerunning tests when working with Sample sequence number mode and without sample barcodes
5 Operation
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Situation before rerun What you need to do What the analyzer does
The sample yielded results and the o Make a note of the sample IDs of the The orders are no longer available in the
results are already validated samples you want to rerun. orders list.
o Choose Routine > Manage test
results.
o Delete the results of the samples you
want to rerun.
o Choose Routine > Manage sample
orders.
o Choose the Create button.
o Enter the rack ID.
o Enter the rack position.
o Choose the test profile, if required.
o Assign the patient, if required.
o Choose the Save button. The new order is created. It gets the next
free sequence number, the deleted
sequence number cannot be re-used.
o Be sure to place the sample on the rack The test is performed.
and position as defined above, then
load the rack.
The STAT sample was placed on a o Choose Routine > Manage test
routine rack results.
o Select the sample and choose the
Rerun button.
o Choose Routine > Manage sample
orders.
o Select the order and choose the Edit
button.
o Adjust the rack ID and the rack The STAT rack ID is entered.
position. Order type is set to STAT .
o Place the rack on the priority rack slot. The rack barcode is read and the sample is
processed.
The routine sample was placed on a o Choose Routine > Manage test
STAT rack results.
o Select the sample and choose the
Rerun button.
o Select the order and choose the Edit
button.
o Adjust the rack ID and the rack The routine rack ID is entered.
position. Order type is set to routine .
o Place the rack on the priority rack slot. The rack barcode is read and the sample is
processed.
y Rerunning tests when working with Sample sequence number mode and without sample barcodes
5 Operation
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188 Non-routine situations
Situation before rerun What you need to do What the analyzer does
You detect a sample mismatch and Reset the sample sequence number and
need to rectify the situation. run all tests of the rack again.
o Choose Routine > Manage sample
sequence numbers.
o Choose the Edit button.
o As the Next sequence No., enter the If you enter a number lower than the next
lowest sample sequence number that free sample sequence number, the results
was used for samples on the rack. Enter of the numbers greater than the one you
it in either the Routine or STAT entry entered are deleted. For example: The next
field, as appropriate. free sample sequence number is 150 and
you enter 140, the results for numbers 140
to 149 are deleted.
If you enter a number higher than the next
free sample sequence number, the
numbers between are blocked. For
example: The next free sample sequence
number is 150 and you enter 160, numbers
150 to 159 are blocked and cannot be used.
o Choose the Save button.
o Place the tubes in the correct potions
on the rack.
o Load the rack. New sample sequence numbers are
assigned to the samples and the tests are
processed.
y Rectifying sample mismatch
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5 Operation
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190 Managing patients
Managing patients
Patient demographics can be defined separately or when
you assign patients. You can assign patients to results
and orders, and you can change patient demographics
later.
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5 Operation
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192 Routine maintenance actions
NOTICE
Malfunction due to failure of performing due
maintenance actions
Failing to perform maintenance actions that are due may
impair the functioning of the analyzer.
r Always perform all maintenance actions as soon as
they become due.
NOTICE
Damage to the analyzer due to use of inappropriate
cleaning solution
Using inappropriate cleaning solutions may damage the
parts you cleaned.
r Only use recommended cleaning solutions.
u Cleaning solutions (113)
r Never use the wash solution for manually cleaning the
analyzer.
5 Operation
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Routine maintenance actions 193
To check for tasks that need doing you can use the
Tasks and Overview groups in the Overview work area.
In this section
Checking the status of order processing (194)
Checking for tasks that need doing (194)
Checking the current hardware status (195)
Checking the status of supplies (196)
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194 Routine maintenance actions
1
1 Check the task indicator and the task list in the
Overview work area for red or orange items.
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Routine maintenance actions 195
Color Meaning
Red There is at least one issue that requires
immediate operator attention. Operation may
have stopped.
Orange There is at least one issue that requires early
operator attention. Operation may otherwise
stop.
Light There are no current issues. The hardware
gray element works fine.
1
1 In the Overview work area, choose the analyzer in the
Overview illustration.
f A schematic representation of key hardware
elements is displayed.
f The color of the elements represents the severity of
the underlying issues.
2
2 In the analyzer overview, choose a colored element.
I A callout is displayed containing a description of
the issue and possibly a wizard button. The
described issue is the one with the highest priority.
5 Operation
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196 Routine maintenance actions
Status Meaning
Error All analyzer activities have stopped. An exceptional
hardware situation has occurred, for example a
connector is unplugged.
Alarm All analyzer activities have stopped. The situation
can be resolved by user intervention, for example by
refilling some consumable.
Warning Operator intervention is required as soon as
possible, otherwise processing may stop, for
example when the system water level gets low.
OK Everything is fine. No intervention is required.
y List of statuses
1
1 Choose Monitoring > Manage supplies.
I In the Status column, the status is indicated.
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Routine maintenance actions 197
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198 Routine maintenance actions
Air purge
Air purge is periodically performed to remove any
possible air pockets in the tubing. This is achieved by
pumping system water through the whole fluid system.
You may also need to perform this action as a result of a
message in the message list or as part of troubleshooting.
u To define how frequently automatic air purge is
performed see Defining the operating
environment (264).
5 Operation
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Routine maintenance actions 199
! CAUTION
Incorrect results due to using unsuitable system
water
Using unsuitable system water may influence the
measured values and lead to incorrect results.
r Always use water of the specified quality:
u Water quality (112)
NOTICE
Analyzer damage due to using unsuitable system
water
5 Operation
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200 Routine maintenance actions
! CAUTION
Incorrect results due to not using the wizard
Failing to use the Fill water container wizard when
refilling water may lead to air bubbles in the fluid system,
which may lead to incorrect pipetting and consequently
to incorrect results.
r Always use the Fill water container wizard when
refilling water.
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Routine maintenance actions 201
NOTICE
Incorrect fill level indication and analyzer damage
due to re-insertion of non-empty waste container
Fill level monitoring is performed with the help of a
counter. When you confirm that you have emptied the
container, the counter is reset to zero.
If the solid waste container is full, test strips may get
stuck in the waste chute and interfere with the measuring
mechanism.
r Always empty the waste container before you confirm
its emptying and placing it on the analyzer again.
NOTICE
Incorrect counters due to not using the wizard
Failing to use the Empty solid waste container wizard
when emptying the solid waste may lead to incorrect
counters and consequently to inaccurate fill level
warnings. If the solid waste container is full, test strips
may get stuck in the waste chute and interfere with the
measuring mechanism.
r Always use the Empty solid waste container wizard
when emptying the solid waste.
! CAUTION
Personal injury due to touching internal mechanism
If the solid waste container is removed, parts of the rack
transport mechanism can be accessed from the opening
for the solid waste container. If you insert your hands
while the analyzer is processing, you may get your fingers
5 Operation
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202 Routine maintenance actions
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Routine maintenance actions 203
! CAUTION
Incorrect results due to deteriorated test strip
quality
The test strip cassette compartment is designed to
maintain a constant low humidity. Exposing the test strip
cassette to the general laboratory environment air may
lead to rapid water uptake by the pads on the test strips
and so change their chemical characteristics, which may
lead to incorrect results.
r Always load the test strip cassette within 3 minutes
after removing it from its airtight packaging. Follow
the instructions given in the Instructions for Use.
r Do not open the test strip cassette compartment
unless you are going to replace the test strip cassette.
r Be sure to always close firmly the cassette
compartment door.
NOTICE
Test strip handling error due to touching of test
strips
Touching test strips may deform them and cause
handling problems.
r Do not touch test strips inside the test strip cassette.
NOTICE
Damage to test strips and test strip cassettes due to
inappropriate handling
Trying to force the test strip cassette into the test strip
cassette compartment may damage the test strips and
the test strip cassette.
r Do not force the test strip cassette into the
compartment. Be sure to align it properly and follow
the instructions given in the wizard.
r Do not shake or drop the test strip cassette.
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204 Routine maintenance actions
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At the end of the shift 205
In this section
Logging off (205)
Shutting down the analyzer (206)
Keeping the analyzer clean (208)
Logging off
Only one user can be logged on the analyzer at any time.
You can log off any time, even while the analyzer is
processing tests.
r To log off
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206 At the end of the shift
! CAUTION
Loss of data due to using the power switch
Switching off the analyzer by pressing the on/off switch
or the power switch does not allow for an orderly
software shut-down and may lead to loss of data.
r Do not use the on/off switch or the power switch to
shut down the analyzer, instead use the Shut down
button on the Overview work area.
! CAUTION
Incorrect results due to using the on/off or the
power switch while processing tests
Switching off the analyzer while processing tests does not
allow for an orderly software shut-down and may lead to
incorrect results and to loss of data.
r Do not use the on/off switch or the power switch
while processing is going on.
In this section
Shutting down the analyzer (206)
Putting the analyzer into standby (207)
Switching off the power supply (208)
NOTICE
Possible analyzer damage due to using the on/off
switch
Using the on/off switch during shutdown may cause
hard-disk damage.
5 Operation
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At the end of the shift 207
screen anywhere.
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208 At the end of the shift
2
2 Put the power switch at the back of the analyzer in the
A
off position .
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At the end of the shift 209
! CAUTION
Skin inflammation or injury caused by working
solutions
Direct contact with cleaning solutions or other working
solutions may cause skin irritation, inflammation, or
burns.
r If a cleaning solution or other working solution comes
into contact with your skin, wash it off immediately
with water and apply disinfectant. Consult a physician.
NOTICE
Damage to the analyzer due to use of inappropriate
cleaning solution
Using inappropriate cleaning solutions may damage the
parts you cleaned.
r Only use recommended cleaning solutions.
u Cleaning solutions (113)
r Never use the wash solution for manually cleaning the
analyzer.
NOTICE
Damage to the analyzer due to excessive liquid
Any liquid spilled on the analyzer may result in
malfunction or damage.
r Do not spray any liquid on any of the analyzer
surfaces.
5 Operation
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210 At the end of the shift
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At the end of the shift 211
1
1 Wipe the rack conveyors near the input and output
buffers using a paper towel moistened with cleaning
solution.
2
2 Fold down the rack transport rail. Hold the rail at both
ends and pull it out firmly.
! WARNING
Infection by samples and associated materials
Contact with samples containing material of human origin
may result in infection. All materials and mechanical
components associated with samples of human origin are
potentially biohazardous.
r If any biohazardous material is spilled on the rack tray
surface, wipe it up immediately and apply disinfectant.
5 Operation
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212 At the end of the shift
! WARNING
Personal injury and infection due to the edges on
the rack tray’s center guide rail
The edges on the rack tray’s center guide rail may cause
personal injury and infection.
r Avoid contact with all edges, even when wearing lab
gloves.
r Wear personal protective equipment such as lab
gloves.
r Carefully observe all instructions given in this task.
1
1 Use personal protective equipment when cleaning the
rack tray.
A B C D
A Rail edge C Rail center
B Rail grove D Rack tray
2
2 Wipe the rail center in both directions with a cotton
swab moistened with cleaning solution.
• If there is sticking and crystallized dirt on the rack
tray, scrape it with a cotton swab.
5 Operation
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At the end of the shift 213
3
3 Wipe the rail edge in both directions with a cotton
swab moistened with cleaning solution.
• If there is sticking and crystallized dirt on the rack
tray, scrape it with a cotton swab.
4
4 Wipe the rail groove in both directions with a cotton
swab moistened with cleaning solution.
• If there is sticking and crystallized dirt on the rack
tray, scrape it with a cotton swab.
5
5 Wipe the edges on the bottom of the rack tray in both
directions with a cotton swab moistened with cleaning
solution.
• If there is sticking and crystallized dirt on the rack
tray, scrape it with a cotton swab.
6
6 Wipe the surface of the rack tray, starting from the
center in both directions with an at least 10 mm thick
pile of lint-free cloth moistened with cleaning solution.
• Hold the rack tray with one hand, the pile of lint-
free cloth with your fingers, and wipe the surface
of the rack tray.
5 Operation
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214 At the end of the shift
7
7 Wipe the rear surface of the rack tray, starting from
the center in both directions with an at least 10 mm
thick pile of lint-free cloth moistened with cleaning
solution.
• Hold the rack tray with one hand, the pile of lint-
free cloth with your fingers, and wipe the surface
of the rack tray.
8
8 Wipe the bottom surface of the rack tray, starting from
the center in both directions with an at least 10 mm
thick pile of lint-free cloth moistened with cleaning
solution.
• Hold the rack tray with one hand, the pile of lint-
free cloth with your fingers, and wipe the surface
of the rack tray.
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5 Operation
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216 At the end of the shift
A Groove
! WARNING
A
Incorrect results and malfunction due to damaged
test strip tray or transporter
A Hook
Incorrect handling, for example knocking or dropping,
may damage the test strip tray and test strip transporter.
r Handle the test strip tray and transporter with care.
r Make sure you do not drop the test strip tray or
transporter and place them gently when putting them
down.
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At the end of the shift 217
1
1 Pull out the test strip transporter (A).
A B
2 Pull out the test strip tray (B).
4 Wipe the test strip transporter and the test strip tray
using a paper trowel moistened with cleaning
solution.
5 Dry the test strip transporter and the test strip tray
using a dry paper towel.
I Leave the parts to dry completely.
6
6 Insert the test strip tray in the two support pins (B)
B A B and push it firmly in.
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218 At the end of the shift
1
1 Wipe the test strip pipetting area using a paper towel
moistened with ethanol.
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At the end of the shift 219
Cleaning the analyzer housing and the input and output buffers
5 Operation
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220 Calibrating the photometer unit
External target value Each pad of the calibration strip has its defined
reflectance value (supplied with the calibration strip).
Internal target value, correction factor To actually calibrate the analyzer, a dedicated calibration
strip is used, for which the values for each pad are known
(external target values). During the calibration process,
both the calibration strip pads and the built-in reference
plate are measured. Then, for each pad on the calibration
strip, the relation between the calibration strip pad results
and the built-in plate results is established (internal target
value) and compared with the external target values. This
results in the correction factor.
Result calculation (reflectance values) For each test, the reference plate and all the pads on the
test strip are measured and for each pad the relation
between the results of the reference plate and the test
pad is established and then multiplied with the correction
factor.
No valid calibration The system performs plausibility checks for the results. If
no valid calibration result can be established, calibration
must be repeated, otherwise performing tests is not
possible.
u For information on how to proceed if calibration is still
5 Operation
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Calibrating the photometer unit 221
! WARNING
Incorrect results due to biased calibration results
Soiling on calibration strips may influence the calibration
results and consequently impair the validity of the test
results.
r Do not touch the pads of the calibration strips and
avoid placing them on any surface other than the test
strip transporter.
r Do not re-use calibration strips. Always use a new
calibration strip for each calibration, including repeats.
5 Operation
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222 Calibrating the measuring cell
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QC tasks 223
QC tasks
When the lot of the QC material expires or the QC test has
failed a message is added to the message list. Tests are
still performed but the test results are marked with Q in
the column.
w Displaying a QC message
In this section
Performing QC measurements (223)
Reviewing QC results (230)
Performing QC measurements
In this section
About performing QC measurements (224)
Preparing the QC rack (224)
Performing a QC measurement (225)
Performing a QC measurement when working with an
LAS (225)
5 Operation
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cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
224 QC tasks
! CAUTION
Incorrect results due to sample mix-up
Tubes on QC racks are not individually identified. It is
assumed that the fluids are valid and placed as defined in
the QC rack definitions.
r Be sure to use the QC material that has been defined
on the analyzer.
r Be sure to fill the tubes with the prescribed QC
materials and place them on the predefined positions.
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QC tasks 225
Performing a QC measurement
r To perform a QC measurement
Defining QC materials
5 Operation
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226 QC tasks
About defining a new QC material by reading • If the new QC material has more levels than the
the RFID tag currently defined maximum number, this maximum
number is automatically increased to the number of
levels of the new QC material.
• If the number of QC levels of the new QC material is
different from that of the current QC material, a yellow
message is generated.
• If the number of QC levels is higher than the defined
maximum level, there are no current QC results for the
highest level and you need to perform QC. Check the
yellow messages.
• If the number of QC levels is smaller than the defined
maximum level, change the number of QC levels to
reflect the number of levels coming from the QC RFID.
u To define the number of QC levels (263)
When reading the RFID tag the following data are read
and stored on the analyzer:
• QC level
• Target ranges
• Lot number
• Expiry date
5 Operation
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QC tasks 227
2
2 Present the RFID tag of the QC material to the RFID
reader at a distance of between 1 and 25 mm (0.04-
1 in).
f The QC material data are registered and displayed
on screen.
6
6 If you want to use the QC material straight away you
need to activate it: select the material and choose the
Activate/deactivate button.
f Active materials are marked with in the Active
column.
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228 QC tasks
5
5 If you want to use the QC material straight away you
need to activate it: select the material and choose the
Activate/deactivate button.
I Only one lot can be active per QC level. Lots that
have expired are automatically deactivated.
Active materials are marked with in the Active
column.
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QC tasks 229
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230 QC tasks
Deleting QC materials
r To delete QC materials
Reviewing QC results
Possible result symbols
Passed
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QC tasks 231
Not passed
Color coding
Green The result is within target range.
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232 QC tasks
r To review QC results
1
1 Choose Routine > Manage QC > Review QC
results.
f The results are displayed.
r To delete QC results
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QC tasks 233
5 Operation
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234 Additional operating tasks
In this section
Stopping and restarting sample processing (234)
Changing the password (235)
Removing the test strip cassette (236)
Printing and exporting information, generating
reports (237)
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Additional operating tasks 235
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236 Additional operating tasks
! CAUTION
Incorrect results due to deteriorated test strip
quality
The test strip cassette compartment is designed to
maintain constant low humidity. Exposing the test strip
cassette to the general laboratory environment air may
lead to rapid water uptake by the pads on the test strips
and so change their chemical characteristics, which may
lead to incorrect results.
r Always reload the test strip cassette immediately after
removing it from an analyzer.
NOTICE
Test strip handling error due to manual touching of
test strips
Touching test strips may deform them and cause
handling problems.
r Do not touch test strips inside the test strip cassette.
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Additional operating tasks 237
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238 Additional operating tasks
f A callout is displayed.
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Additional operating tasks 239
5 Operation
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240
5 Operation Additional operating tasks
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241
Table of contents
Configuration 6
In this chapter 6
User management . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 243
Defining a new user . . . . . . . . . . . . . . . . . . . . . . . . . 243
Changing user data . . . . . . . . . . . . . . . . . . . . . . . . . 245
Resetting the password . . . . . . . . . . . . . . . . . . . . . . 246
Activating and deactivating a user . . . . . . . . . . . . . 246
System settings: Defining the test environment. . . . . 247
About system settings . . . . . . . . . . . . . . . . . . . . . . . 247
Defining the units in which results are displayed
and reported . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 249
Defining the order in which test parameters are
shown. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 249
Defining the validation method . . . . . . . . . . . . . . . 250
Defining cross-check rules . . . . . . . . . . . . . . . . . . . 251
Defining a cross-check rule . . . . . . . . . . . . . . . 251
Changing a cross-check rule . . . . . . . . . . . . . . 252
Deleting a cross-check rule . . . . . . . . . . . . . . . 253
Managing the result storage capacity . . . . . . . . . . 253
Defining how the sample IDs are generated . . . . 254
Defining range tables. . . . . . . . . . . . . . . . . . . . . . . . 254
6 Configuration
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242
Table of contents
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cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
User management 243
User management
User management consists of the following tasks:
• Defining new users
• Changing user data
• De-activating users
• Defining new passwords
• Resetting passwords
In this section
Defining a new user (243)
Changing user data (245)
Resetting the password (246)
Activating and deactivating a user (246)
o User configuration
o System settings (test definition, profiles)
o User interface language installation
o System configuration (operating system,
communication)
o Screen sharing
Service In addition to all actions of the User and
Supervisor groups, users with Service rights
can perform the following tasks:
o Software installation
y List of user group rights
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244 User management
User statuses
Status Description
Active The user can log on to the analyzer.
Inactive The user cannot log on to the analyzer but remains
on the analyzer and can be activated any time.
u Activating and deactivating a user (246)
y List of user statuses
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User management 245
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246 User management
deactivated instead.
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System settings: Defining the test environment 247
Roche Diagnostics
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248 System settings: Defining the test environment
System settings
Result presentation
Measurement settings QC settings 'HIDXOWWHVWSURÀOH
settings
u 601 • Delete
• Activate/deactivate
• Report
Change test result order • Create
in report • Referenced range table u 601
Cross-check rules
u 601
• Rule name
• Suggestion
• Items
General
• Storage limit
• Warning limit
• If database is full
Sample ID
• Generation mode
Multiple measurement
• Number of measurements
u 601
Range tables
5DQJHWDEOHFRQÀJXUDWLRQ
/LPLWFRQÀJXUDWLRQ
&RORUUDQJHFRQÀJXUDWLRQ
6 Configuration
Available to all users Item To new screen, panel, or callout • Item Item, function summary
Available to users with Supervisor rights only Item Panel on same screen
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System settings: Defining the test environment 249
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250 System settings: Defining the test environment
Validation methods
Methods Description
Automatic All results are automatically validated.
validation of all If you work with a LIS validated results
are automatically sent to the host.
Automatic All results are automatically validated,
validation rules unless an additional condition (rule)
applies, (a cross-check rule was
triggered, a trace, sieve, or SG alarm
was generated, an abnormal result was
6 Configuration
generated).
If you work with a LIS validated results
are automatically sent to the host.
Manual validation All results must be validated manually.
y List of validation methods
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System settings: Defining the test environment 251
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252 System settings: Defining the test environment
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System settings: Defining the test environment 253
changed.
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254 System settings: Defining the test environment
Generation modes
Mode Description
Barcode Use this value if you work with sample
barcodes and the sample ID is
contained in your sample barcodes.
Sample sequence Use this value if you do not work with
number sample barcodes.
y Generation modes
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System settings: Defining the test environment 255
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256 System settings: Defining the test environment
In this section
Choosing the range table (256)
Defining a new range table (256)
Making changes to range tables (258)
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7 Choose a parameter.
f The current ranges are displayed in the detail
panel.
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258 System settings: Defining the test environment
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System settings: Defining the test environment 259
Limit configuration
Value ranges and limits are used to determine whether a
result is positive or negative and whether to trigger data
alarms and actions such performing additional tests.
1+ 2+ 3+ 4+ 5+
1+ 2+ 3+ 4+ 5+
A B
A Limit for trace data alarm B Limit for abnormal data alarm
1+ 2+ 3+ 4+ 5+
6 Configuration
A B
A Limit for abnormal data alarm B Upper limit for sieve data alarm
Lower limit for sieve data alarm
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260 System settings: Defining the test environment
1+ 2+ 3+ 4+ 5+
A B
A Limit for abnormal data alarm B Upper limit for sieve data alarm
Lower limit for sieve data alarm Results within the range of 1+ and 3+ trigger a sieve data
alarm
1+ 2+ 3+ 4+ 5+
A B C
A Limit for trace data alarm C Upper limit for sieve data alarm
Lower limit for sieve data alarm Results ≥ 1+ trigger a sieve data alarm
B Limit for abnormal data alarm
1+ 2+ 3+ 4+ 5+
A B C
A Limit for trace data alarm C Upper limit for sieve data alarm
B Limit for abnormal data alarm Results ≥ 2+ trigger a sieve data alarm
Lower limit for sieve data alarm
range tables.
u To define a new range table (256)
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System settings: Defining the test environment 261
Limit values
Value Description
Trace value Value that defines when a sample
should have a follow-up test. It must be
≤ Abnormal value.
Abnormal value Values ≥ this value are outside the
normal or trace range. It must be ≥
Trace value.
Sieve lower limit Values ≥ this value trigger an additional
test.
Sieve upper limit Values ≤ this value trigger an additional
test.
y Limit values
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262 System settings: Defining the test environment
1
1 Choose Administration > System settings
> Measurement settings > u 601 > Color range
configuration.
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System settings: Defining the test environment 263
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264 System configuration: Defining the operating environment
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
System configuration: Defining the operating environment 265
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6 Configuration
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266 System configuration: Defining the operating environment
NOTICE
Basic configuration 1 items
Using both virtual and external keyboard
Using the virtual keyboard and the external keyboard at
the same time could lead to operating complications.
r Do not use both keyboards at the same time.
Item Description
System name Any alphanumeric characters. This is
displayed in the global information area.
Language de: German
selection(1) en: English
es: Spanish
fr: French
it: Italian
ko: Korean
pl: Polish
pt: Portuguese
ru: Russian
tr: Turkish
zh: Chinese
Only the installed languages are
available.
Password mode o Simple password mode: The
password is defined manually
during user definition. It cannot be
changed by the general user.
o Strong password mode: The
system generates a random
6 Configuration
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System configuration: Defining the operating environment 267
Item Description
Enable virtual Clear the check box if you want to use
keyboard the external keyboard instead of the
virtual keyboard.
Enable automatic If you select the check box also enter a
logoff time-out value between 1 and
1000 minutes.
y Basic configuration 1 items
(1) This list is not necessarily complete, further languages may become
available and different languages may be installed on your analyzer.
u Related topics
• Performing basic configuration (267)
u Related topics
6 Configuration
r To perform configuration
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268 System configuration: Defining the operating environment
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System configuration: Defining the operating environment 269
! CAUTION
Incorrect results due to undetected reading errors
Barcode reading errors could potentially go undetected if
a checksum is not used, which could lead to sample
mismatch.
r Use only barcodes with checksum.
r Use only barcode labels of a good print quality.
Barcodes contain Enable checksum check? Transmit and show checksum characters?(1)
checksum characters?
Yes
The checksum character is transmitted to the host and also included
in the sample ID.
Yes Yes
No
The checksum character is not transmitted to the host and it is not
included in the sample ID.
No No(2) No
checked.
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270 System configuration: Defining the operating environment
Port settings
Port Description
c 6500 Host protocol versions 8 and older.
c 6500_09 Host protocol versions 9 or more recent.
This version is not backward compatible
with version 8 and older.
y Port settings
You can define default values for the content of the report
header, the printer, the analyzer whose results should be
reported, the file location and the type of reporting you
want to use.
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System configuration: Defining the operating environment 271
Parameter Description
Report header The Report header definitions are used for patient
reports.
Title e.g. facility name.
Subtitle 1 e.g. laboratory name.
Subtitle 2 e.g. department name.
Printer settings Printer Printer that is connected to the analyzer or any defined
network printer.
Report creation The Report creation definitions are used as default
values in all reports. They can be changed during report
creation.
File path The paths the user can select when saving data to files or
creating a report. It must be a mapped network drive.
Axeda is intended for direct upload to Roche Service.
Output mode Print: Send the report to the printer.
PDF: Save the report as a PDF file.
Report condition Automatic: Generate a report for every result.
Data alarm: Generate a report for results with the data
alarms listed in Assigned data alarms. (To include a data
alarm in this list, choose the data alarm from the Available
data alarms drop-down list and then choose the Create
button. To remove the data alarms from the list, choose the
Clear button.)
Manual: Only generate a report when requested to do so.
y Report items
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272 System configuration: Defining the operating environment
Code Definition
de German
en English
es Spanish
fr French
it Italian
ko Korean
pl Polish
pt Portuguese
ru Russian
tr Turkish
zh Chinese
y Language codes
Code Definition
de German
en English
es Spanish
fr French
y User interface languages
(1) This list is not necessarily complete, further languages may become
available and different languages may be installed on your analyzer.
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System configuration: Defining the operating environment 273
Code Definition
it Italian
pl Polish
pt Portuguese
ru Russian
tr Turkish
zh Chinese
y User interface languages
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274 System configuration: Defining the operating environment
Importing system settings You can import system settings that were previously
exported, even if they were saved with a different
software version. In the latter case, you need to have
installed software version 2.1.1 or more recent.
• If the configuration file to be imported contains an
item that does not exist in the current setup it is
ignored and not imported.
• If a setting value does not exist in the configuration
file to be imported, but is defined in the current
software, the default value is set during next software
startup.
System settings report The system settings report provides the system settings in
an easily readable form.
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6 Configuration
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276 Managing racks
Managing racks
You can define STAT racks, QC racks, and wash racks,
which means that STAT testing, QC testing and the wash
action start automatically as soon as you place such a
rack on the input buffer. This is achieved by assigning
certain rack IDs to the STAT testing, QC testing and wash
actions.
u Rack IDs (81)
! WARNING
Sample mismatch due to inconsistent rack ID
definition
It may be possible that you have several racks with the
same rack ID. For a given analyzer, rack IDs must be
unique.
r Make sure that the rack IDs that you assign to STAT
racks are not used at the same time for routine racks
that might be processed on your analyzer.
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Managing racks 277
r To define a QC rack
6 Configuration
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278 Adjusting the probe action
This ensures that the probe does not touch the tube
bottom and that it is properly immersed in liquid when
aspiring.
You perform this task with the help of the Adjust rack
and tube wizard.
The values for the sample rack are automatically valid for
the QC rack as well, therefore, no QC rack needs to be
prepared.
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Maintenance
7 Maintenance ..........................................................................................................281
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281
Table of contents
Maintenance 7
In this chapter 7
Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 283
Routine maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . 284
Miscellaneous maintenance actions . . . . . . . . . . . . . . 287
Cleaning the water container . . . . . . . . . . . . . . . . . 287
Managing the result storage capacity . . . . . . . . . . 288
Keeping your data safe . . . . . . . . . . . . . . . . . . . . . . 290
About exporting and importing the setup
data. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 290
Backing up the database. . . . . . . . . . . . . . . . . . 291
Issues with the probe. . . . . . . . . . . . . . . . . . . . . . . . 292
If you are not going to use the analyzer for some
time. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 294
7 Maintenance
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Table of contents
7 Maintenance
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Safety 283
Safety
! Read and understand the information in the
Safety chapter
Warning messages:
u Biohazardous materials (27)
u Waste (27)
Caution messages:
u Mechanical safety (30)
u Working solutions (30)
u Influence of vibrations (31)
Notice messages:
u Spillage (33)
u Excessive ambient humidity (33)
NOTICE
Damage to the analyzer due to use of inappropriate
cleaning solution
Using inappropriate cleaning solutions may damage the
parts you cleaned.
r Only use recommended cleaning solutions.
u Cleaning solutions (113)
r Never use the wash solution for manually cleaning the
analyzer.
7 Maintenance
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284 Routine maintenance
Routine maintenance
All routine maintenance actions can be performed using
wizards. They are grouped into actions relating to
consumables (supplies) and actions related to keeping
the analyzer working (maintenance).
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Routine maintenance 285
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286 Routine maintenance
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Miscellaneous maintenance actions 287
In this section
Cleaning the water container (287)
Managing the result storage capacity (288)
Keeping your data safe (290)
Issues with the probe (292)
If you are not going to use the analyzer for some
time (294)
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288 Miscellaneous maintenance actions
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Miscellaneous maintenance actions 289
4 Choose a destination.
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290 Miscellaneous maintenance actions
r To delete results
In this section
About exporting and importing the setup data (290)
Backing up the database (291)
7 Maintenance
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Miscellaneous maintenance actions 291
7 Maintenance
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292 Miscellaneous maintenance actions
! WARNING
Incorrect results due to touching the probe
Touching the probe with bare fingers may leave residues
on its surface and consequently influence the accuracy of
the results.
r Do not touch the probe except for maintenance as
described in this documentation.
! CAUTION
Skin inflammation or injury caused by working
solutions
Direct contact with cleaning solutions or other working
solutions may cause skin irritation, inflammation, or
burns.
r If a cleaning solution or other working solution comes
into contact with your skin, wash it off immediately
with water and apply disinfectant. Consult a physician.
! CAUTION
Personal injury due to contact with sharp objects
r Avoid contact with the probe tip.
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Miscellaneous maintenance actions 293
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294 Miscellaneous maintenance actions
If you are not going to use the analyzer for some time
Supplies that remain on the analyzer for a long time may
deteriorate. Therefore, if you intend not to use the
analyzer for some time, Roche recommend removing
them from the analyzer.
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Miscellaneous maintenance actions 295
7 Maintenance
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296
7 Maintenance Miscellaneous maintenance actions
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Troubleshooting
8 Troubleshooting ....................................................................................................299
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299
Table of contents
Troubleshooting 8
In this chapter 8
Exceptional situations . . . . . . . . . . . . . . . . . . . . . . . . . . 301
Screenshots. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 303
Log files . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 304
No photometer calibration can be generated. . . . . . . 306
No measuring cell calibration can be generated . . . . 306
Detached barcode labels. . . . . . . . . . . . . . . . . . . . . . . . 307
Recovering from an irregular stop . . . . . . . . . . . . . . . . 308
Emergency stop . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 309
When you have accidentally pulled the waste
drawer during operation . . . . . . . . . . . . . . . . . . . . . . . . 311
Recovering from a power outage . . . . . . . . . . . . . . . . . 312
Safety interlock . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 314
8 Troubleshooting
Clogged inlet water filter . . . . . . . . . . . . . . . . . . . . . . . . 314
Blocked floats . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 317
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Table of contents
8 Troubleshooting
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Exceptional situations 301
Exceptional situations
The following table lists, in alphabetical order, exceptional
situations that may occur and points to ways of how to
handle them.
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302 Exceptional situations
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Screenshots 303
Screenshots
As part of troubleshooting, in particular if you need to
contact a Roche Service representative, it is useful to
generate screenshots to capture the exact situation at the
time of a problem occurring.
r To generate a screenshot
8 Troubleshooting
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304 Log files
Log files
All activities on the analyzer are recorded in log files.
Message log All users can view the message log, which contains a
chronological log of all messages that were generated by
the analyzer, including the task messages.
Audit trail Users with Supervisor user rights can also view the audit
trail, which contains a chronological log of all activities
and events such as logon, logoff, order handling, sample
processing, result validation, QC, calibration,
maintenance, software updates, and remote access, as
well as those concerning configuration.
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Log files 305
8 Troubleshooting
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306 No photometer calibration can be generated
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Detached barcode labels 307
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308 Recovering from an irregular stop
! CAUTION
Loss of data and sample due to turning off the
analyzer using the on/off switch
Pressing the on/off switch for several seconds stops all
processing and shuts down the internal PC. No status
information can be stored. Incomplete tests and other
activities will have to be redone.
r Do not use the on/off switch to turn off the analyzer
except in an emergency, e.g. when the screen is
“frozen” and analyzer does not react to any user
action, on-screen or otherwise.
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Emergency stop 309
5 Check the task list and deal with all red and orange
items.
5 Check the task list and deal with all red and orange
items.
orders. (u 185)
Emergency stop
Use this function if, for some reason, all activities on the
analyzer must be stopped immediately or if the analyzer is
stuck in either the Operating or Init status.
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310 Emergency stop
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When you have accidentally pulled the waste drawer during operation 311
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312 Recovering from a power outage
! CAUTION
Incorrect results due to power outage
Accidentally unplugging the power supply or a power
outage stops all processing. If as a result the test strip
cassette shutter remains open, ambient air can enter the
test strip cassette and influence the chemistry of the test
pads.
r Ensure that the mains cables are placed safely away
from areas where personnel might pass through.
r Roche recommends using an uninterruptible power
supply.
u Uninterruptible power supply (UPS) (111)
6 Check the task list and deal with all red and orange
items.
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Recovering from a power outage 313
8 Troubleshooting
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314 Safety interlock
Safety interlock
! WARNING
Immediate processing stop due to opening the main
cover
Opening the main cover results in immediate power
interruption to all units and processing stop.
r Do not open the main cover during routine operation.
clogged.
u To clean the inlet water filter (315)
u To clean the inlet water filter (external water
supply) (316)
m Check whether the inside of the water container is
soiled or shows deposits.
u To clean the water container (287)
u To clean the water container for external water
supply (288)
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cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4
Clogged inlet water filter 315
A
A
B B
C C
2 Before you fill the container with water, rinse the inlet
water filter with 1% NaOCl.
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316 Clogged inlet water filter
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Blocked floats 317
Blocked floats
It may happen that the floats in the water and liquid
waste containers do not move freely any more or that they
might be blocked. In such situations, the level indications
as indicated by messages might not agree with the actual
levels.
! CAUTION
Contamination of the environment by liquid and
solid waste
The waste of the analyzer is potentially biohazardous and
must be treated in accordance with the relevant laws and
regulations.
r When disposing of any waste, do so in accordance
with the appropriate local regulations.
r Any substances contained in QC materials and other
working materials, which are legally regulated for
environmental protection, must be disposed of in
accordance with the relevant water discharge facility
regulations. For the legal regulations on water
discharge, please contact the suppliers of the
materials.
! CAUTION
Infection by liquid waste
Contact with liquid waste may result in infection. All
materials and mechanical components associated with
the waste systems are potentially biohazardous.
r Be sure to wear protective equipment. Take extra care
when working with lab gloves; these can easily be
pierced or cut, which can lead to infection.
r If any biohazardous material is spilled, wipe it up
8 Troubleshooting
immediately and apply disinfectant.
r If liquid waste comes into contact with your skin, wash
it off immediately with water and apply disinfectant.
Consult a physician.
r Observe the safety labels on the equipment.
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318 Blocked floats
2
2 Remove the water tubing adapter (A) from the water
container and place it on a clean surface.
A
3 Hold one of the floats (B) with two fingers and gently
move it back and forth along the float assembly rod.
They should move freely.
I Observe the status of the message on screen,
depending on the position of the float it should
change its color.
Do the same with the other float.
2
2 Remove the water tubing adapter (A) from the water
container and place it on a clean surface.
A
8 Troubleshooting
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Blocked floats 319
3
3 Hold one of the floats (B) with two fingers and gently
move it back and forth along the float assembly rod.
They should move freely.
I Observe the status of the message on screen,
depending on the position of the float it should
B change its color.
Do the same with the other float.
3
3 Remove the waste tubing adapter (A) from the liquid
waste container and place it on a clean surface.
A
4 Empty the liquid waste. Dispose of it in accordance
with the appropriate local regulations.
B
5 Hold one of the floats (B) with two fingers and gently
B move it back and forth along the float assembly rod.
They should move freely.
I Observe the status of the message on screen,
depending on the position of the float it should
8 Troubleshooting
change its color.Do the same with the other float.
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320
8 Troubleshooting Blocked floats
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Glossary
9 Glossary ...................................................................................................................323
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Glossary 323
Analyte - Work area
Glossary 9
The glossary lists terms that are used in the user Wash solution Liquid used for internal washing the
documentation that may not be familiar to the reader fluid system.
or that carry meaning that is specific to this analyzer
environment. Work area Part of the screen, usually a tab, that
groups related information and tasks for the
Analyte See Urine analyte. convenience of the user, for example tasks relating to
performing tests or to setting up the analyzer.
Arbitrary units Result classification using 1+, 2+, 3+
classes instead of numerical concentration results.
Calibration strip Gray plastic strip used for
calibrating the photometer.
Callout Popup window that is displayed on screen to
show information or to accept user input as part of
performing a certain task.
Cleaning solution Liquid used for cleaning and
decontamination of surfaces and parts of a system.
Compensation pad A blank white pad on the test
strip that is used for establishing the intrinsic color of
the urine with the purpose of compensation for this
color value to prevent false results with strongly
colored urine samples.
Failsafe image Failsafe images are photometer
images that are created when a photometer errors
occurs. They are intended for Roche Service
representatives only.
Priority rack Any rack that is placed on the priority
rack slot for immediate processing.
Qualitative determination The measurement of
analytes or features with descriptive (qualitative) result
classification such as negative/positive.
Radio frequency identification (RFID) tag
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324
9 Glossary
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Index
Index..........................................................................................................................327
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Index 327
Index
– buttons, 138
Buttons, colors, 138
– messages, 122
– QC results, 231
C – results, 138
Components, 63
Calibrating – optional, 114
– measuring cell, 222, 306 Conditions
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328 Index
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Index 329
Fatigue, 32 K
Fill water container, wizard, 200
Film on sample, 28 Keyboard, connecting, 134
Filter, 314 Keyboard, specifications, 114
Filtering information, 130
Flags
– See, Data alarms
L
Floats,blocked, 317
Labels
Fluid system, 89
– detached, 307
– removing air, 198
– stuck in transport unit, 307
– washing, 197
Labels on analyzer, 34
Foam on sample, 28
Language, 266
Footprint, 110
– changing, 272
Forced shutdown, 309
– installing, 272
Formats, date and time, 267
Levels, QC, 263
Fuses, 33
Limits
– defining, 259
G – defining for warnings, 262
Liquid containers, overview, 83
Global information area, 121 Liquid waste containers, overview, 85
Liquids
– connectors, 69
H List of tasks, 50
Loading
Handling
– priority racks, 166, 167
– See, Working with
– racks, 160
Hardware status, 195
– racks with input connection unit, 162
Heat output, 111
Location, 267
Help, 139
Log files, 304
Host connections, defining, 270
– viewing, 304
Humidity, 31, 33
Logging off, 205
Logging on, 153
I Logoff, automatic, 266
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330 Index
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Index 331
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332 Index
Short guide, daily operation, 51, 52, 149 System configuration, 265
Shutting down the analyzer, 206 System name, 266
Size, analyzer, 110 System settings, 247
Software – exporting, 274
– installed, 275 – importing, 273
– third-party, 24
Solid waste containers
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Index 333
T V
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334
Index Index
Roche Diagnostics
cobas u 601 urine analyzer · Software Version 2.3 · Operator’s Manual · Version 2.4