Users Manual

B-life / Pro B-life / Co B-life

Manual resuscitators with R Valve

B-life Pro B-life Co B-life

0123 This appliance conforms with the Directive 93/42/CEE Medical Devices

Guarantee of Quality system for the production and the final control of the products certified by the notifying body TV
SD Product Service GmbH

INDEX

General informations page 2 Operating instructions page 5

Warnings page 2 Maintenance and cleaning page 6
Description of product page 4 Accessories and spare parts page 7

First edition: 02/03/09

Rev. 3: 26/08/15

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 Thank you for choosing a Spencer product

1. GENERAL INFORMATION
1.1 Aim and contents
The aim of this manual is to supply all the information necessary so that the client, will not only attain adequate use of the
appliance, he will also be capable of using the instrument in the most autonomous and secure way possible. This includes
information regarding technical aspects, functioning, maintenance, spare parts and safety.

1.2 Conservation of the instruction and maintenance manual

The instruction and maintenance manual must be kept together with the product, for the whole life of the device, inside a
dedicated container and above all, away from any substances or liquids which could compromise perfect legibility.

1.3 Symbols used

Symbol Meaning

General or specific warnings

See instructions for use

Lot number

Product code

The product is compliant with the specifications of the Directive 93/42/CEE

Single use

1.4 Servicing request

For any information regarding the correct interpretation of the instruction manual, the use, maintenance, installation and restore
of the product, please contact the Spencer Customer Care Service tel. 0039 0521 541111, fax 0039 0521 541222, e-mail
[email protected] or write to Spencer Italia S.r.l. - Strada Cavi, 7 - 43044 Collecchio (Parma) - ITALY. In order to facilitate the
assistance service, please always indicate the lot number (LOT) shown on the label applied on the box or on the device.

1.5 Demolition
When the devices are no more suitable for being used, if they havent been contaminated by any particular agents, they can be
disposed of as normal solid waste, otherwise follow the current regulations about demolition.

1.6 Labelling
Each device has got an identifying label, positioned on the device itself and/or on the box. This label includes information about
the manufacturer, the product, the CE mark, the lot number (LOT). It must never be removed or covered.

2. WARNINGS
2.1 General warnings
The product must be used by trained personnel only, having attended specific training for this device and not for similar
products.
Training routines must be registered on a special register in which the names of those trained, of the trainers, date and place
are indicated. This register which will certify the eligibility of the operators to use the Spencer device has to be kept for a
period of 10 years after the disposal of the device itself. This register will be made available to the competent authorities
and/or manufacturer if requested.
Spencer Italia S.r.l. is always at your disposal to plan trainings on products.
Before carrying out any kind of operation on the appliance (training, installation, use), the operator must carefully read the
enclosed instructions, paying particular attention to the correct safety precautions and to the procedures to be followed for
installation and for correct use.
If the instructions belong to another device and not to the device received, inform the manufacturer immediately and avoid
use of the device.
In case of any doubts about the correct interpretation of the instructions, please contact Spencer Italia S.r.l. for any necessary
clarifications.
Do not allow untrained persons to help during the use of the device, because they could cause damage to the patient or to
themselves.
Regularly check the appliance, carry out the prescribed maintenance and respect the average life span, as indicated by the
manufacturer in this users manual.
Before each use of device the perfect operating state of the device must be checked as specified in the instruction manual. If
any damage or abnormalities which could in any way influence the correct functioning and the safety of the device, of the

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 patient and of the user are detected, the device must be immediately removed from service and the manufacturer must be
contacted.
If any failure or incorrect functioning of the device is detected, it must be immediately substituted with a similar item so that
the rescue procedures are guaranteed without any interruption.
Use of the device in anyway other than described in this manual is forbidden.
Do not alter or modify in any way the appliance; any such interference could cause malfunctions and injury to the patient
and/or rescuer.
The appliance must not in any way be tampered with (modification, adjustment, addition, replacement). In such cases all
responsibility will be denied for any malfunctions or injuries caused by the appliance itself; moreover CE certification and
product warranty will be considered void.
Those who modify or have modified, prepare or have prepared medical appliances in such a way that they no longer serve the
purpose for which they were intended, or no longer supply the intended service, must satisfy the valid conditions for the
introduction onto the market.
Handle with care.
Ensure that all the necessary precautions are taken in order to avoid the hazards that can arise as the result of contact with
blood or body fluids.
Register and store with these instructions: lot number, place and date of purchase, first date of use, date of checks, name of
users, any comments.
When the device is being used, the assistance of qualified staff must be guaranteed.
Do not store the device underneath any heavy objects which could cause structural damage.
Store in a cool, dry, dark place and do not expose to direct sun.
Store and transport device in its original packaging.
The device not be exposed to or come into contact with any source of combustion or inflammable agents.
Position and adjust the device taking care not to cause any obstruction to rescuers and or any other rescue equipment.
Attention: laboratory testing, post production tests, instruction manuals cannot always consider every possible scenario for
use. This means that in some cases the performance of the product could be notable different from results to date obtained.
Instructions are continually being updated and are under tight surveillance of fully qualified staffs with adequate technical
formation.
With reference to the D. Lgs. 24th February 1997, n. 46 emended by D. Lgs. 25/01/2010, n. 37 Acknowledgement of
Directive 93/42/CEE and 2007/47/CE, we remind both public and private operators that they are obliged to report any
accident that involves any medical device to the Ministry of Health and to the Manufacture as specified and within time given
by the European regulations.
In addition, both public and private operators are obliged to inform the manufacturer of any measures that should be
adopted to make the steps necessary to guarantee the safety and the health of the patients and the users o any medical
device.
As a distributor or end user of products manufactured and/or marketed by Spencer Italia S.r.l., you are strictly required to
have a basic knowledge of any legal requirements applying to the devices contained in this supply that are in power in the
goods final destination Country (including laws and norms regarding technical specifications and/or safety requirements) and
therefore you are also strictly required to have the necessary knowledge to guarantee all aspects regarding the total
conformity of the products to the regulations in the relevant territory.
Promptly notify Spencer Italia S.r.l. regarding any revisions to be made by manufacturer in order to guarantee the conformity
of the product to the territorys legal specifications (including those resulting from rules and/or norms of other nature).
Act, with all due care and diligence, and contribute to ensure conformity to general safety requirements of all devices
marketed in the territory, by providing final users with all necessary information for carrying out periodical checks on their
devices, as specified in the relevant users manual.
Actively contribute to product safety checks on products sold, by communicating any relevant risk analysis information both
to the manufacturer and to any competent authorities so that the necessary action can be promptly taken.
The distributor or final user is aware that in the event of any failure to conform to the above mentioned requirements you will
be deemed fully responsible for all damages that might occur. Therefore Spencer Italia S.r.l. expressly disclaims any
responsibility and/or liability for your non-compliance with the present regulatory provisions.

2.2 Specific warnings

The manual resuscitators must be used only by operators who have been adequately trained in the techniques of cardio-
pulmonary resuscitation (CPR or ACLS).
The device should not come into contact or be in any way exposed to sources of heat or inflammable agents.
The oxygen supply in the presence of hydrocarbons will generate an explosive mix.
Do not use the device in a contaminated atmosphere.
Do not administrate or enrich with oxygen in the presence of fire or sparks.
Remove the reservoir if enrichment with oxygen is not necessary.
Do not use lubricants (e.g. oils or greases) on any part of the manual resuscitator.
Check the state of the products on opening the product and before each use.
Do not dismantle the overpressure valve.

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2.3 Contraindications and side effects
The use of these devices, if used by operators who have been adequately trained in the techniques of cardio-pulmonary
resuscitation (CPR or ACLS), does not present any contraindications or collateral effects.

3. DESCRIPTION OF PRODUCT
3.1 Intended use
The manual resuscitators B-life, Pro B-life and Co B-life have been designed to offer adequate assistance to patients during the
CPR and assisted ventilation manoeuvres.
They can be used efficiently and safely to maintain pulmonary ventilation in case of reanimation and in other critical situations
when spontaneous respiration is insufficient or absent.
The B-BAG manual resuscitators can be used to supply oxygen when connected to a source of oxygen. In order to guarantee
a high percentage of oxygen, the manual resuscitator is supplied complete with a valve and reservoir.
The percentage of oxygen supplied to the patient depends on:
flow
current volume
frequency
technique being used

3.2 Main components

The manual resuscitators B-life, Pro B-life and Co B-life are available in three different sizes: adult, paediatric and infant.

Fig. A

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3.3 Models
These basic models could be modified, with reference to codes and/or descriptions without any previous notification.

3.3.1 B-life models (without face mask and reservoir)

BG03020A B-life Resuscitation bag in silicone, adult, with R Valve
BG03021A B-life Resuscitation bag in silicone, adult, with overpressure valve and R Valve
BG03022A B-life Resuscitation bag in silicone, paediatric, with R Valve
BG03023A B-life Resuscitation bag in silicone, paediatric, with overpressure valve and R Valve
BG03024A B-life Resuscitation bag in silicone, infant, with R Valve
BG03025A B-life Resuscitation bag in silicone, infant, with overpressure valve and R Valve

3.3.2 Pro B-life models (without face mask and reservoir)

BG02006A Pro B-life Resuscitation bag in PVC, adult, with R Valve
BG02007A Pro B-life Resuscitation bag in PVC, adult, with overpressure valve and R Valve
BG02008A Pro B-life Resuscitation bag in PVC, paediatric, with R Valve
BG02009A Pro B-life Resuscitation bag in PVC, paediatric, with overpressure valve and R Valve
BG02018A Pro B-life Resuscitation bag in PVC, infant, with R Valve
BG02019A Pro B-life Resuscitation bag in PVC, infant, with overpressure valve and R Valve

3.3.3 Co B-life models (without face mask and reservoir)

BG08100A Co B-life Resuscitation bag in PVC, adult, with R Valve
BG08000A Co B-life Resuscitation bag in PVC, adult, with overpressure valve and R Valve
BG08101A Co B-life Resuscitation bag in PVC, paediatric, with R Valve
BG08001A Co B-life Resuscitation bag in PVC, paediatric, with overpressure valve and R Valve
BG08105A Co B-life Resuscitation bag in PVC, infant, with R Valve
BG08010A Co B-life Resuscitation bag in PVC, infant, with overpressure valve and R Valve

3.4 Technical data

Resuscitators B-LIFE (silicone) PRO-B-LIFE (PVC) CO-B-LIFE (PVC)

Item Adult Paediatric Infant Adult Paediatric Infant Adult Paediatric Infant
Resuscitator Silicone Silicone Silicone PVC PVC PVC PVC PVC PVC
Diaphragm valve Silicone Silicone Silicone PVC PVC PVC PVC PVC PVC
Reservoir bag PVC PVC PVC PVC PVC PVC PVC PVC PVC
Overpressure valve Stainless Stainless Stainless Stainless Stainless Stainless Stainless Stainless
Stainless steel
spring steel steel steel steel steel steel steel steel
Patient valve PS PS PS PC PC PC PC PC PC
Reservoir valve PC/Silicone PC/Silicone PC/Silicone PC/Silicone PC/Silicone PC/Silicone PC/Silicone PC/Silicone PC/Silicone
Nominal Bag 1600 ml 500 ml 280 ml 1600 ml 500 ml 280 ml 1600 ml 500 ml 280 ml
volume Reservoir 2500 ml 2500 ml 600 ml 2500 ml 2500 ml 600 ml 2500 ml 2500 ml 600 ml
Dead space 7 ml 7 ml 7 ml 7 ml 7 ml 7 ml 7 ml 7 ml 7 ml
60 5 40 5 40 5 60 5
Overpressure valve 40 5 mbar 60 5 mbar 40 5 mbar 40 5 mbar 40 5 mbar
mbar mbar mbar mbar
Packing Not sterile Not sterile Not sterile Not sterile Not sterile Not sterile Not sterile Not sterile Not sterile
Max stroke volume 900 ml 250 ml 130 ml 900 ml 250 ml 130 ml 900 ml 250 ml 130 ml
Max cycling rate 45 bpm 100 bpm 95 bpm 45 bpm 100 bpm 95 bpm 45 bpm 100 bpm 95 bpm

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3.4 Reference standards
Reference Title of document
MDD 93/42/CEE European Directive about Medical Devices
Modifications to 90/385/CEE Directive about active implants, Directive 93/42/CEE
MDD 2007/47/CEE about medical devices and Directive 98/8/CE about the introduction of biocides onto
the market
Legislative Decree 24/02/1997, n. 46 Application of the 93/42/CEE Directive about Medical Devices
Legislative Decree 25/01/2010, n. 35 Modifications and additions to the 20/02/97 Decree n. 46
Medical devices Quality management systems Requirements for regulamentary
UNI EN ISO 13485
purposes
UNI EN ISO 14971 Application of risks managing to medical devices
Medical devices - Symbols for use in the medical device labels, labelling and
UNI CEI EN ISO 15223-1
information to be provided. Part 1: general requirements
UNI CEI EN 1041 Information supplied by the medical devices manufacturer
Medical Devices - Application of the utilisation characteristics of engineering to medical
CEI EN 62366
devices
MEDDEV 2.4/1a-b Guideline for the classification of medical devices
NB-MED 2.5.1 /Rec 5 Technical Documentation
MEDDEV 2.7.1 Clinical Data
MEDDEV 2.12/1 Medical Devices vigilance system
Clinical evaluation of the medical devices for human beings - Part 2: Clinical evaluation
UNI EN 14155
plans
EN ISO 10651-4 Lung ventilators -- Part 4: Particular requirements for operator-powered resuscitators

3.5 Environmental conditions

Environmental conditions B-life (silicone) Pro B-life (PVC) Co B-life (PVC)

Functioning temperature (C) from -18 to + 50 from 0 to +50 from 0 to +50

Storage temperature (C) from -30 to +60 from -20 to +50 from -20 to +50

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4. OPERATING INSTRUCTIONS
4.1 Transport and storage
Before transporting the appliance, make sure that it is correctly packaged ensuring also that there are no risks of shocks, bumps
or falls during the transport itself.
Keep the original packaging for use in case of any further transport and for storage. Damage to the appliance caused during
transport and handling is not covered by the guarantee. Repairs or replacement of the damaged parts are the responsibility of
the client. The device must be stored in a dry, cool area away from direct sunlight. It must not be placed in contact with any
substances or chemical agents which could cause damage and reduce safety characteristics.

4.2 Preparation
On receipt of the product:
Remove the packaging and display the material so that all components are visible.
Check that all the components/pieces on the accompanying list are present.

The appliance must be checked before every use so as to reveal any working abnormalities and/or damage caused by transport
and/or storage.

4.3 Functioning test

Fig. B

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4.4 Use
Make sure the patient is in a safe place and position the mask over the patient's face and nose and hold it in place with
index finger and thumb.
Using the other hand, ventilate the patient by squeezing rhythmically the bag, as prescribed by your standard area protocols.

Clear the airways removing if necessary any vomit, liquid or foreign bodies that may obstruct them.
Manual resuscitators can be connected to a fix or mobile source of oxygen.

The gas supplied to the patient can be enriched with oxygen:

Connect a no crush oxygen tube between the connection on the reservoir valve and the flowmeter of the oxygen cylinder
or central oxygen supply.
Regulate the flow so that during the insufflation phrase (patient inspiring) the reservoir fills up completely and it collapses
during the expiratory phrase.

If enrichment with oxygen is not required and/or there is no source of oxygen, remove the reservoir.
On attaching the resuscitator to the oxygen source make sure that the reservoir expands.
In a contaminated atmosphere, use only oxygen for patient reanimation.
The condition of the patient must always be under constant control.
To select the overpressure valve, (if included) press and turn (as shown in the
figure).
Should the overpressure valve become contaminated with blood, vomit or any
type of secretion, remove the resuscitator from use and continue to ventilate
the patient with the aid of a single direction mouth to mouth mask/valve.
Before using a mouth to mouth valve we advise to disconnect the resuscitator
from the patient and strongly squeeze the resuscitator to remove any liquid
from the patient valve.
Check that the valve is clean and in this case continue to ventilate with the
resuscitation bag.
On terminating resuscitation, clean and sterilize (where possible) and test the
device as described in this manual.

Fig. C

4.5 Troubleshooting
PROBLEM CAUSE REMEDY
The chest does not expand correctly Obstructions of the airways caused by Free the airways by manually
during ventilation foreign bodies removing any foreign bodies
The head is not correctly extended Place the patients head in the correct
position according to the CPR
procedures
The mask does not adhere perfectly to Reposition the mask following the
the patients face instructions and press slightly to
improve adherence
Air leakage from components of the Check that all components of the
resuscitation bag resuscitator are correctly assembled
together
One of components is damaged Immediately remove the device from
service and contact your Assistance
Centre
The mask leaks air even though The patient has moustache/beard or If the face is sweaty try to clean and
correctly positioned his skin is sweaty dry face. In the case of beard or
moustache, increase the pressure on
the mask

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5. MAINTENANCE AND CLEANING
5.1 Cleaning
During cleaning and assembly of the device, Personal Protection Equipment (PPE) should be used.
After use, clean and disinfect the B-life, Pro B-life e Co B-life manual resuscitator as follows.
Dismantle the resuscitator from the mask and wash all parts with water and a mild detergent. Make sure that the detergent is
compatible with the material of the resuscitator. Rinse under running warm water making sure to remove all traces of detergent.
Do not remove the overpressure valve as it could cause permanent damage.
The reservoir is a single use product and cannot be sterilized. Dispose after use.

Pro B-life (PVC) Co B-life (PVC)

Cleaning method B-life (silicone)
single use single use
Boiling for 6 minutes
Yes No No
Autoclave maximum Ref.UNI EN 554
Yes No No
Autoclave rubber cycle Ref.UNI EN 554
Yes No No
Ethylene oxide Ref.UNI EN 550
Yes No No
Liquid sterilizer
Yes Yes Yes

Failure to carry out correctly the cleaning procedure could be a cause of cross infection due to the presence of secretions
and/or residuals on the device.

5.2 Maintenance
5.2.1 Precautionary maintenance
The person who carries out the precautionary maintenance of the appliance (user in person, Manufacturer/supplier or a third
party) has to guarantee the following basic requirements:
Technical knowledge of the appliance and of the periodic maintenance procedures as described in these instructions.
Specific qualifications and training in the maintenance operations of the appliance in question.
The use of components/replacement parts/accessories that are either original or approved by the supplier, in such a way
that each operation causes no alteration or modification to the appliance.
Possession of the checklist of operations carried out on the appliance.
Guarantee complete adherence to the instructions of the Directive 93/42/CEE which includes also the obligation towards the
Manufacturer to maintain post sales records and traceability of the appliance if requested.

The operator must always wear adequate personal protection such as gloves and mask etc. during all checking and cleaning
procedures.

Checks to be carried out before and after each use, and at least every 3 months, are as follows:
General functionality of the device
Cleanliness of the device (remember that the failure of cleaning may cause the risk of cross infections)
Absence of cuts, holes, tears on the structure
Status of wear and damage to the device due to the number of sterilization cycles undergone.
Expiration date or average life span, if any.

Planned interventions by the Manufacturer or authorized center are not required, but it is prescribed to make cleaning and
checking indicated in the specific sections "Cleaning" and "Precautionary Maintenance".
If the correct revision is not carried out, the CE branding will no longer be considered valid as the product will no longer be
compliant with the 93/42/CE Directive for Medical Devices and consequently it is no longer compliant with the safety standards
declared by the Manufacturer at time of purchase.

For disposable devices is necessary to check the expiration date/life span, but there are no cleaning and maintenance
activities, being non-reusable devices.

5.2.3 Special servicing

Only the Manufacturer or centres with written authorisation are authorised to complete any special servicing operations.
For any operations that are not carried out directly by the Manufacturer but by an authorised centre, we have to underline that a
report regarding all operations carried out must be requested. This will permit both Spencer Italia S.r.l. and the end user to keep
a log book regarding the operations carried out on the device.

The device, if used as indicated in the following instruction manual, has an average life span of 5 years.

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Spencer Italia S.r.l. will accept no responsibility for the incorrect functioning and/or damage caused by the use of any device
which has not been repaired, or certified on expiry date by the Manufacturer or by one of the Manufacturer's Authorised Servi ce
centres, making void both the guarantee and the conformity to the Medical Devices Directive 93/42/CEE.

6. ACCESSORIES AND SPARE PARTS

6.1 Accessories and spare parts
RM20400A Spencer Mask Face masks in polysulphonate size 0 soft
RM20800A Spencer Mask Face masks in polysulphonate size 0
RM20802A Spencer Mask Face masks in polysulphonate size 2
RM20804A Spencer Mask Face masks in polysulphonate size 4
RM20805A Spencer Mask Face masks in polysulphonate size 5
RM20810B Spencer Mask Kit Face masks in polysulphonate, four sizes
RM20400A Spencer Mask Face masks in polycarbonate size 0 soft
RM20700A Spencer Mask Face masks in polycarbonate size 0
RM20702A Spencer Mask Face masks in polycarbonate size 2
RM20704A Spencer Mask Face masks in polycarbonate size 4
RM20705A Spencer Mask Face masks in polycarbonate size 5
RM20710B Spencer Mask Kit Face masks in polycarbonate, four sizes
RM20400B B-life Face masks in silicone size 0
RM20401B B-life Face masks in silicone size 1
RM20402B B-life Face masks in silicone size 2
RM20403B B-life Face masks in silicone size 3
RM20404B B-life Face masks in silicone size 4
RM20405B B-life Face masks in silicone size 5
RM10860A Air Cuffed Mask Single patient mask without valve , PVC, size 0, 10 pcs
RM10861A Air Cuffed Mask - Single patient mask without valve, PVC, size 1, 10 pcs
RM10862A Air Cuffed Mask - Single patient mask without valve, PVC, size 2, 10 pcs
RM10863A Air Cuffed Mask - Single patient mask without valve, PVC, size 3, 10 pcs
RM10864A Air Cuffed Mask - Single patient mask without valve, PVC, size 4, 10 pcs
RM10865A Air Cuffed Mask - Single patient mask without valve, PVC, size 5, 10 pcs
RM10870A Air Cuffed Mask - Single patient mask with valve, PVC, size 0, 10 pcs
RM10871A Air Cuffed Mask - Single patient mask with valve, PVC, size 1, 10 pcs
RM10872A Air Cuffed Mask - Single patient mask with valve, PVC, size 2, 10 pcs
RM10873A Air Cuffed Mask - Single patient mask with valve, PVC, size 3, 10 pcs
RM10874A Air Cuffed Mask - Single patient mask with valve, PVC, size 4, 10 pcs
RM10875A Air Cuffed Mask - Single patient mask with valve, PVC, size 5, 10 pcs
EV60030C EVX 30 PEEP valve, autoclavable
EV60032C EVX 32 PEEP valve, single patient
EV50010C EVX 10 Non-rebreathing valve, single use
EV50012C EVX 12 Non-rebreathing valve, autoclavable
EV50007C EVX 07 Non-rebreathing valve, autoclavable, paediatric/infant 40 cmH2O
EV50008C EVX 08 Non-rebreathing valve, single use, paediatric/infant 40 cmH2O
EV50009C EVX 09 Non-rebreathing valve, single use, adult 60 cm H2O
EV50011C EVX 11 Non-rebreathing valve, autoclavable, adult 60 cm H2O
BG03094A OX V/R Oxygen aspiration valve and reservoir, adult/paediatric, autoclavable for B-life
BG02032A OX V/R Oxygen aspiration valve and reservoir, adult/paediatric, single use for Pro B- life and Co B- life
BG03095A OX V/R Oxygen aspiration valve and reservoir, infant, autoclavable for B-life

It is absolutely important to indicate if the replacement parts are needed for adult, paediatric or infant sizes.

Warning
The information contained in this document could be modified without any warning and is not to be intended as a commitment on behalf of Spencer Italia S.r.l.
Spencer products are exported to many countries and the same identical regulations are not always valid. For this reason there could be differences between the
description here described and the product actually delivered. Spencer continually strives to reach the perfection of all items sold. We therefore hope you will
understand if we reserve the right, at any time, to modify the shape, equipment, lay-out or technical aspects that are herein described.

Copyright Spencer Italia S.r.l.

All rights reserved.
No part of this document can be photocopied, reproduced or translated into another language without the written approval of Spencer Italia S.r.l.

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