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C.R. Bard 10-010116

by Bosma Enterprises

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 Number10818634025620 UDI-DI Date14 May 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  • Withdrawn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
C.R. Bard
Generic name
Single-administration urethral drainage catheter
Model / Ref / Catalog
10-010116
Primary DI / UDI-DI
10818634025620
FDA product code
KOD
GMDN term
Single-administration urethral drainage catheter
Device class
Class II
Regulation number
876.5130
GUDID distribution status
In Commercial Distribution
Size
Catheter Gauge — 16 French

Other devices from Bosma Enterprises

See all devices from Bosma Enterprises →

Properties

  • Supplied sterile
  • Single use
  • Contains latex
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date

Other properties (8)

  • Sterilise before use: No
  • Implantable: No
  • Over-the-counter: No
  • Convenience kit: No
  • Combination product: No
  • HCT/P: No
  • Serial number: No
  • Manufacturing date: No