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Olympus WA94005A

by Olympus Winter & Ibe GmbH

Olympus WA94005A is a Class II device made by Olympus Winter & Ibe GmbH, listed in FDA GUDID since 31 Jul 2020 (UDI-DI 14042761083451), 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 Number14042761083451 UDI-DI Date31 Jul 2020ListedStatusListed 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  • Withdrawn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
Olympus
Generic name
Inert gas-enhanced endoscopic electrosurgical electrode, single-use
Model / Ref / Catalog
WA94005A
Primary DI / UDI-DI
14042761083451
FDA product code
GEI
GMDN term
Inert gas-enhanced endoscopic electrosurgical electrode, single-use
Device class
Class II
Regulation number
878.4400
GUDID distribution status
In Commercial Distribution

Related devices

Category: Inert gas-enhanced endoscopic electrosurgical electrode, single-use

Similar devices in this category

Other devices filed under Inert gas-enhanced endoscopic electrosurgical electrode, single-use.

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)