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Biopsy Valve MD-495

by Olympus Medical Systems Corporation 2 variants

Biopsy Valve MD-495 is an endoscope working-channel valve (FDA Class II; FDA product code FDS, Gastroscope and accessories, flexible/rigid) made by Olympus Medical Systems Corporation, listed in FDA GUDID since 21 Sep 2016 (UDI-DI 04953170064111), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04953170064111 UDI-DI Date21 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Biopsy Valve
Generic name
Endoscope working-channel valve, reusable
Model / reference
MD-495
Primary DI / UDI-DI
04953170064111
FDA product code
FDS
GMDN term
Endoscope working-channel valve, reusable
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code FDS (Gastroscope and accessories, flexible/rigid).

Other devices from Olympus Medical Systems Corporation

See all devices from Olympus Medical Systems Corporation →

Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (11, all answered No)