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UbiqVue Multiparameter UB2551

by LifeSignals, 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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB353UB25511 UDI-DI Date20 Jul 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  • Withdrawn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
UbiqVue Multiparameter
Generic Name
Wearable multiple physiological parameter recorder, single-use
Model / Reference
UB2551
Primary DI / UDI-DI
B353UB25511
FDA Product Code
DRG, FLL, MHX
GMDN Term
Wearable multiple physiological parameter recorder, single-use
Device Class
Class II
Regulation Number
870.2910, 880.2910, 870.1025
GUDID distribution status
In Commercial Distribution
MRI Safety
MR Unsafe

Other devices from LifeSignals, Inc.

See all devices from LifeSignals, Inc. →

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

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