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date
08/05/2022
page 1 of 3
MODEL: CPE-422AC | DESCRIPTION: PIEZO BUZZER INDICATOR
FEATURES
• wire leads with panel-mount tabs
• 220 Vac
• 92 dB
• 3 kHz frequency
SPECIFICATIONS
parameter
conditions/description
min
rated voltage
max
units
250
Vac/Vdc
13
mA
220
operating voltage
current consumption
typ
60
at rated voltage
rated frequency
2,500
sound pressure level
at 30 cm, rated voltage
dimensions
Ø41.8 x 22
ABS UL94 1/16” HB High Heat
terminal
wire leads
3,500
92
Hz
dB
mm
weight
material
3,000
Vac
22.5
g
operating temperature
-30
85
°C
storage temperature
-40
95
°C
RoHS
Notes:
yes
1. All specifications measured at 5~35°C, humidity at 45~85%, under 86~106kPa pressure, unless otherwise noted.
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CUI DEVICES | MODEL: CPE-422AC | DESCRIPTION: PIEZO BUZZER INDICATOR
date 08/05/2022 | page 2 of 3
MECHANICAL DRAWING
units: mm
tolerance: ±0.5 mm
3.4
(2 PLCS)
7.0
UL1007 LF 24AWG
5.0
59.5
2.0
red
red
140.0
50.0
41.8
10.0
22.0
PERFORMANCE CURVES
P: Voltage vs. Sound Pressure Level
I: Voltage vs. Current Consumption
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CUI DEVICES | MODEL: CPE-422AC | DESCRIPTION: PIEZO BUZZER INDICATOR
date 08/05/2022 | page 3 of 3
REVISION HISTORY
rev.
description
date
1.0
initial release
11/12/2007
1.01
brand update
12/16/2019
logo, datasheet style update
08/05/2022
1.02
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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