Cma 4544pf W PDF
Cma 4544pf W PDF
Cma 4544pf W PDF
date
09/24/2013
page
1 of 4
conditions/description
directivity
omnidirectional
sensitivity (S)
min
typ
max
units
-46
-44
-42
dB
10
Vdc
operating voltage
output impedance (Zout)
f = 1 kHz, 1 Pa
2.2
-3
dB
frequency (f)
20
Hz
0.5
mA
60
operating temperature
storage temperature
dimension
20,000
dBA
-20
70
-20
70
0.8
9.7 x 4.5 mm
weight
material
Al
terminal
RoHS
yes
Note:
We use the Pascal (Pa) indication of sensitivity as per the recomendation of I.E.C. (International Electrotechnical Commission). The sensitivity of Pa will increase 20dB
compared to the ubar indication. Example: -60dB (0dB = 1V/ubar) = -40dB (1V/Pa)
MECHANICAL DRAWING
MEASUREMENT CIRCUIT
unit: mm
RL = 2.2 K
Schematic Diagram
cui.com
1.000V/PA
MECHANICAL CHARACTERISTICS
item
test condition
evaluation standard
No interference in operation.
vibration test
drop test
ENVIRONMENT TEST
item
test condition
evaluation standard
thermal shock
TEST CONDITIONS
standard test conditions
a) Temperature: +5 ~ +35C
b) Humidity: 45 ~ 85%
a) Temperature: +25 2C
b) Humidity: 60 ~ 70%
cui.com
PACKAGING
cui.com
REVISION HISTORY
rev.
description
date
1.0
initial release
06/01/2008
1.01
09/24/2013
The revision history provided is for informational purposes only and is believed to be accurate.
Headquarters
20050 SW 112th Ave.
Tualatin, OR 97062
800.275.4899
Fax 503.612.2383
cui.com
[email protected]
CUI offers a one (1) year limited warranty. Complete warranty information is listed on our website.
CUI reserves the right to make changes to the product at any time without notice. Information provided by CUI is believed to be accurate and reliable. However, no responsibility is
assumed by CUI for its use, nor for any infringements of patents or other rights of third parties which may result from its use.
CUI products are not authorized or warranted for use as critical components in equipment that requires an extremely high level of reliability. A critical component is any component of a
life support device or system whose failure to perform can be reasonably expected to cause the failure of the life support device or system, or to affect its safety or effectiveness.