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Disposable Biopsy Forceps Fb-231K

by Olympus Medical Systems Corporation 2 variants

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 Number04953170158049 UDI-DI Date21 Sep 2016ListedStatusListed 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  • Withdrawn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
Disposable Biopsy Forceps
Generic Name
Flexible endoscopic biopsy forceps, single-use
Model / Reference
FB-231K
Primary DI / UDI-DI
04953170158049
FDA Product Code
FCL
GMDN Term
Flexible endoscopic biopsy forceps, single-use
Device Class
Class I
Regulation Number
876.1075
GUDID distribution status
In Commercial Distribution

Related devices

Category: Flexible endoscopic biopsy forceps, single-use

Other devices from Olympus Medical Systems Corporation

See all devices from Olympus Medical Systems Corporation →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date

Other properties (8)

  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No