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08/05/2022
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MODEL: CPE-6080 | DESCRIPTION: PIEZO BUZZER TRANSDUCER
FEATURES
• piezo transducer wire leads
• 80 dB SPL
• 800 Hz rated frequency
SPECIFICATIONS
parameter
conditions/description
min
typ
operating voltage
current consumption
at 10 Vp-p, 800 Hz square wave
rated frequency
max
units
50
Vp-p
10
mA
800
sound pressure level
at 10 cm, 10 Vp-p, 800 Hz square wave
electrostatic capacity
at 120 Hz/1 V
dimensions
Ø44.0 x 14.0
80
49,000
dB
70,000
PA-777D (black)
terminal
wire leads
91,000
pF
mm
weight
material
Hz
12
g
operating temperature
-30
80
°C
storage temperature
-40
80
°C
RoHS
Notes:
yes
1. All specifications measured at 5~35°C, humidity at 45~85%, under 86~106kPa pressure, unless otherwise noted.
SOLDERABILITY
parameter
conditions/description
min
typ
max
units
hand soldering
for 2 ± 0.5 seconds
280
290
300
°C
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CUI DEVICES | MODEL: CPE-6080 | DESCRIPTION: PIEZO BUZZER TRANSDUCER
MECHANICAL DRAWING
units: mm
tolerance: ±0.5 mm
wire: UL1007 28 AWG
WEEK
YEAR
FREQUENCY RESPONSE CURVE
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CUI DEVICES | MODEL: CPE-6080 | DESCRIPTION: PIEZO BUZZER TRANSDUCER
date 08/05/2022 | page 3 of 3
REVISION HISTORY
rev.
description
date
1.0
initial release
06/01/2010
1.01
brand update
04/28/2020
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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