Disposable Biopsy Forceps Fb-211D

by Olympus Medical Systems Corporation GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 29 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number04953170466366 UDI-DI	Date17 Jun 2025Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

GUDID

Trade Name: Disposable Biopsy Forceps
Generic Name: Flexible endoscopic biopsy forceps, single-use
Model / Ref / Catalog: FB-211D, N5431840

Primary DI / UDI-DI: 04953170466366
510(k) Number: K250957
FDA Product Code: EOQ
GMDN Term: Flexible endoscopic biopsy forceps, single-use

Device Class: Class II
Regulation Number: 874.4680
GUDID distribution status: In Commercial Distribution

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Properties

Sterile
Single Use
Prescription Use
Lot / Batch Number
Expiration Date

Other properties (9)

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