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Carbou U1-31013A-BR8

by Ningbo kehu Medical Technology Co., Ltd.

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 Number00850088144024 UDI-DI Date14 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  • Withdrawn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
Carbou
Generic Name
Non-adhesive device retention bandage
Model / Reference
U1-31013A-BR8
Primary DI / UDI-DI
00850088144024
FDA Product Code
FQM
GMDN Term
Non-adhesive device retention bandage
Device Class
Class I
Regulation Number
880.5075
GUDID distribution status
In Commercial Distribution

Other devices from Ningbo kehu Medical Technology Co., Ltd.

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Properties

  • Single Use
  • Contains Latex
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Sterile: No
  • Implantable: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No