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Sensinel™ Cpm Wearable ADCP1100-Wb-002

by Analog Devices, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850086928015 UDI-DI Date3 Jun 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name
Sensinel™ Cpm Wearable
Generic Name
Wearable multiple vital physiological parameter monitoring system
Model / Reference
ADCP1100-WB-002
Primary DI / UDI-DI
00850086928015
FDA Product Code
MWI, BZQ, DPS, DQD, DSB, DXH, FLL
GMDN Term
Wearable multiple vital physiological parameter monitoring system
Device Class
Class II
Regulation Number
870.2300, 868.2375, 870.2340, 870.1875, 870.2770, 870.2920, 880.2910
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Other devices from Analog Devices, Inc.

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Properties

  • Prescription Use
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (10)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No