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date
02/21/2020
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MODEL: CLS0362MA-1 │ DESCRIPTION: SPEAKER
FEATURES
•
•
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•
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36 mm
round frame
0.5 W
8Ω
neodymium magnet
mylar cone
SPECIFICATIONS
parameter
conditions/description
min
impedance
at 1.0 kHz, 1.0 V
6.8
resonant frequency (Fo)
at 1.0 V
416
520
input power
frequency response
max
units
0.5
1.0
W
8
9.2
Ω
Fo
sound pressure level
at 1.0 W, 1 m, avg. at 0.8, 1.0, 1.2, 1.5 kHz
distortion
at 2.0 kHz, 0.5 W
buzz, rattle, etc.
must be normal at sine wave
dimensions
Ø36 x 5.0
magnet
Nd-Fe-B
cone material
mylar
terminal
solder pads
89
92
624
Hz
15,000
Hz
95
dB
10
%
2
8.8
operating temperature
-25
hand soldering
for maximum 3 seconds
RoHS
yes
V
mm
weight
Notes:
typ
340
1. All specifications measured at 15~35°C, humidity at 25~75%, under 86~106 kPa pressure, unless otherwise noted.
cuidevices.com
350
g
60
°C
360
°C
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CUI Devices │ MODEL: CLS0362MA-1 │ DESCRIPTION: SPEAKER
units: mm
tolerance: ±0.2 mm
FREQUENCY RESPONSE CURVE
conditions/description
potentiometer range
50 dB
rectifier
RMS
lower limit frequency
20 Hz
wr. speed
100 mm/sec
zero level
60 dB
3D Model
date 02/21/2020 │ page 2 of 3
MECHANICAL DRAWING
parameter
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CUI Devices │ MODEL: CLS0362MA-1 │ DESCRIPTION: SPEAKER
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3D Model
date 02/21/2020 │ page 3 of 3
REVISION HISTORY
rev.
description
date
1.0
initial release
07/20/2007
1.01
brand update
02/21/2020
The revision history provided is for informational purposes only and is believed to be accurate.
CUI Devices offers a one (1) year limited warranty. Complete warranty information is listed on our website.
CUI Devices reserves the right to make changes to the product at any time without notice. Information provided by CUI Devices is believed to be accurate and reliable. However, no
responsibility is assumed by CUI Devices for its use, nor for any infringements of patents or other rights of third parties which may result from its use.
CUI Devices 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.
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