Fentex 049712FX

by FENTEX medical GmbH

Ref 049712FXModel Instrument zum Anschluss an ein Saug- / Spülgerät zur Absaugung von Flüssigkeiten und zur Spülung des Operationsfeldes.

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

CE MDR

Valid until

11 Oct 2031

CE MDR certificate

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

Certifier DQS Medizinprodukte GmbH

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

Region	Authorization	Number	Date	Status
European Union	CE/MDR EUDAMED	Number1000265375	Date12 Oct 2026Issued	StatusActive expires 11 Oct 2031
European Union	CE/MDR EUDAMED	Number42504077200JV Basic UDI-DI 04250407705206UDI-DI	Date7 Sep 2026Registered	StatusActive
United States	GUDID listing GUDID	Number04250407705206 UDI-DI	Date7 Dec 2022Listed	StatusListed GUDID: in commercial distribution

Certificates

1 certificate · EUDAMED

1000265375 Active

Quality management system EU MDR

Certifier

DQS Medizinprodukte GmbH 0297

Issued
12 Oct 2026

Expires
11 Oct 2031

Coverage

2 jurisdictions

Active
Expiring
Withdrawn
Listed
Not covered

European Union CE/MDR Active
United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name: Fentex
Generic Name: Surgical irrigation/aspiration cannula, non-illuminating, reusable
Model / Ref / Catalog: 049712FX, Instrument zum Anschluss an ein Saug- / Spülgerät zur Absaugung von Flüssigkeiten und zur Spülung des Operationsfeldes.
Description: Antrum Cannula by Van Eicken short curved, Luer-Lock 15 cm, Ø 2.5 mm

Primary DI / UDI-DI: 04250407705206
Basic UDI-DI: 42504077200JV
Direct Marketing DI: 04250407705206
FDA Product Code: LRC
EMDN Code: L030101 Suction and irrigation surgical cannulas and handpieces, reusable
GMDN Term: Surgical irrigation/aspiration cannula, non-illuminating, reusable

Device Class: Class IIa EUDAMED
Class I GUDID
Regulation Number: 874.4420
EU market of registration: Germany
GUDID distribution status: In Commercial Distribution

Sterilization Method: Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

Field	EUDAMED	GUDID
Device Class	EUDAMED Class IIa	GUDID Class I

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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