CEP-2280_V01 CUI | Alldatasheet

Document overview

  • Manufacturer or author: Provided By www.digicamel.com(FREE DATASHEET DOWNLOAD SITE)
  • PDF pages: 3

Technical content

MODEL: CEP-2280 │ DESCRIPTION: PIEZO BUZZER INDICATOR cuidevices.com

FEATURES

  • wire leads with panel-mount tabs
  • 12 Vdc rating
  • modulating tones SPECIFICATIONS parameter conditions/description min typ max units rated voltage 12 Vdc operating voltage 6 18 Vdc current consumption at rated voltage 17 mA rated frequency 2,500 3,800 Hz sound pressure level at 30 cm, rated voltage 88 dB tone modulating tones dimensions Ø32.0 x 23.0 mm weight 13.20 g material ABS UL94 1/16” HB (black) terminal wire leads operating temperature -20 60 °C storage temperature -30 70 °C RoHS yes Notes: 1. All specifications measured at 5~35°C, humidity at 45~85%, under 86~106kPa pressure, unless otherwise noted. Additional Resources: Product Page | 3D Model

cuidevices.com CUI Devices │ MODEL: CEP-2280 │ DESCRIPTION: PIEZO BUZZER INDICATOR date 04/23/2020 │ page 2 of 3 MECHANICAL DRAWING units: mm tolerance: ±0.5 mm wire: UL1095 LF 28AWG PERFORMANCE CURVES P: Voltage vs. Sound Pressure Level I: Voltage vs. Current Consumption Additional Resources: Product Page | 3D Model

CUI Devices │ MODEL: CEP-2280 │ DESCRIPTION: PIEZO BUZZER INDICATOR date 04/23/2020 │ page 3 of 3 cuidevices.com 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. rev. description date 1.0 initial release 09/22/2006 1.01 brand update 04/23/2020 The revision history provided is for informational purposes only and is believed to be accurate.

REVISION HISTORY

Additional Resources: Product Page | 3D Model