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Fentex 418825FX

by FENTEX medical GmbH

Ref 418825FXModel Instrument zum Untersuchen.

Fentex 418825FX is a Class I device made by FENTEX medical GmbH, registered in EUDAMED on 7 Sep 2026 (Basic UDI-DI B-04250407734015) and listed in FDA GUDID since 12 Dec 2022 (UDI-DI 04250407734015), active as of 23 Oct 2026.

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

CE MDD

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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-04250407734015 Basic UDI-DI 04250407734015UDI-DIDate7 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04250407734015 UDI-DI Date12 Dec 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04250407734015 registered 7 Sep 2026 Active
  • FDA GUDID UDI-DI 04250407734015 listed 12 Dec 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04250407734015
  2. Registered EUDAMED B-04250407734015

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade name
Fentex
Generic name
Abdominal/ENT/orthopaedic surgical probe, reusable
Model / Ref / Catalog
418825FX, Instrument zum Untersuchen.
Description
Frontal Sinus Seeker by Castelnuovo double-ended, curved 21 cm
Primary DI / UDI-DI
04250407734015
Basic UDI-DI
B-04250407734015
FDA product code
KAK
EMDN code
L149005 ENT probes, reusable
GMDN term
Abdominal/ENT/orthopaedic surgical probe, reusable
Device class
Class I
Regulation number
874.4420
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: ENT probe, reusable

Similar devices in this category

Other devices filed under ENT PROBES, REUSABLE.

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Properties

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