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Fentex 711173FX

by FENTEX medical GmbH

Ref 711173FXModel Starre HNO-Endoskope-Systeme dienen der Diagnostik und chirurgischen Behandlung im HNO-Bereich. Sie ermöglichen die Unte

Fentex 711173FX is a Class I device made by FENTEX medical GmbH, registered in EUDAMED on 7 Sep 2026 (Basic UDI-DI 42504077301K4) and listed in FDA GUDID since 12 Dec 2022 (UDI-DI 04250407748890), active as of 24 Oct 2026.

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Source EUDAMED, GUDID, synced 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number42504077301K4 Basic UDI-DI 04250407748890UDI-DIDate7 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04250407748890 UDI-DI Date12 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI 42504077301K4 registered 7 Sep 2026 Active
  • FDA GUDID UDI-DI 04250407748890 listed 12 Dec 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04250407748890
  2. Registered EUDAMED 42504077301K4

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade name
Fentex
Generic name
Light source adaptor
Model / Ref / Catalog
711173FX, Starre HNO-Endoskope-Systeme dienen der Diagnostik und chirurgischen Behandlung im HNO-Bereich. Sie ermöglichen die Unte
Description
Storz Adapter for Standard telescopes
Primary DI / UDI-DI
04250407748890
Basic UDI-DI
42504077301K4
Direct marketing DI
04250407748890
FDA product code
EQH
EMDN code
Z12021080 ENT endoscopy instruments - hardware accessories
GMDN term
Light source adaptor
Device class
Class I
Regulation number
874.4350
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Endoscopic light source adaptor

Similar devices in this category

Other devices filed under ENDOSCOPIC AND MINIMALLY INVASIVE SURGERY INSTRUMENTS.

Other devices from FENTEX medical GmbH

See all devices from FENTEX medical GmbH →

Properties

  • Sterilise before use
  • Reusable
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (20, all answered No)