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Fentex 530303FX

by FENTEX medical GmbH

Ref 530303FXModel Instrumente zur Erweiterung und Darstellung verschiedener Larynx-Anatomien zur Unterstützung chirurgischer Eingriffe.

Active European Union. Also listed in GUDID (US), not in commercial distribution.

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number42504077302K6 Basic UDI-DI 04250407741204UDI-DIDate7 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04250407741204 UDI-DI Date12 Dec 2022ListedStatusListed GUDID: not in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

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  • Withdrawn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
Rigid optical laryngopharyngoscope
Model / Ref / Catalog
530303FX, Instrumente zur Erweiterung und Darstellung verschiedener Larynx-Anatomien zur Unterstützung chirurgischer Eingriffe.
Description
Operating Laryngoscope by Holinger with light carrier 18 cm
Primary DI / UDI-DI
04250407741204
Basic UDI-DI
42504077302K6
Direct Marketing DI
04250407741204
FDA Product Code
CCW
EMDN Code
Z12021003 Laryngoscopes
GMDN Term
Rigid optical laryngopharyngoscope
Device Class
Class I
Regulation Number
868.5540
EU market of registration
Germany
GUDID distribution status
Not in Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Related devices

Category: Rigid optical laryngopharyngoscope

Other devices from FENTEX medical GmbH

See all devices from FENTEX medical GmbH →

Properties

  • Reusable
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (20)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No