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08/05/2022
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MODEL: CEB-35FD29 | DESCRIPTION: PIEZOELECTRIC DIAPHRAGM
FEATURES
• piezo element
• flexibility to design housing
• feedback loop
SPECIFICATIONS
parameter
conditions/description
min
typ
max
units
30
Vp-p
2,400
2,900
3,400
Hz
500
Ω
operating voltage
resonant frequency
resonant impedance
only for piezo element without wire
electrostatic capacity
at 1 kHz / 1 V
dimensions
Ø35 x 0.63
17,500
brass
terminal
wire type
operating temperature
storage temperature
RoHS
Notes:
32,500
pF
mm
weight
material
25,000
3.5
g
-20
70
°C
-30
80
°C
yes
1. All specifications measured at 5~35°C, humidity at 45~85%, under 86~106kPa pressure, unless otherwise noted.
MECHANICAL DRAWING
units: mm
tolerance: ±0.5 mm
wire: UL 1571 32 AWG
Black
Red
MTGEP36
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Blue
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CUI DEVICES | MODEL: CEB-35FD29 | DESCRIPTION: PIEZOELECTRIC DIAPHRAGM
PACKAGING
units: mm
Inner Box QTY: 300 pcs per box
Carton Size: 550 x 330 x 290 mm
Carton QTY: 3,000 pcs per carton
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3D Model
date 08/05/2022 | page 2 of 3
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CUI DEVICES | MODEL: CEB-35FD29 | DESCRIPTION: PIEZOELECTRIC DIAPHRAGM
date 08/05/2022 | page 3 of 3
REVISION HISTORY
rev.
description
date
1.0
initial release
06/25/2007
1.01
increased depth to 0.63 mm
03/08/2018
1.02
brand update
03/16/2020
logo, datasheet style update
08/05/2022
1.03
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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