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Carbou U1-20955A-BR20

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 Number00850088144093 UDI-DI Date1 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  • Withdrawn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
Wearable percutaneous catheter/tube holder, single-use
Model / Ref / Catalog
U1-20955A-BR20, 120950-20
Primary DI / UDI-DI
00850088144093
FDA Product Code
KGX
GMDN Term
Wearable percutaneous catheter/tube holder, single-use
Device Class
Class I
Regulation Number
880.5240
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