Skip to content

4712348

by Richard Wolf GmbH

Ref 4712348Model 10000201319

4712348 is a device classified as Class I in the EU and Class II in the US made by Richard Wolf GmbH, registered in EUDAMED on 5 Oct 2026 (Basic UDI-DI B-04055207048757) and listed in FDA GUDID since 28 Jun 2017 (UDI-DI 04055207048757), 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-04055207048757 Basic UDI-DI 04055207048757UDI-DIDate5 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207048757 UDI-DI Date28 Jun 2017ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207048757 registered 5 Oct 2026 Active
  • FDA GUDID UDI-DI 04055207048757 listed 28 Jun 2017 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207048757
  2. Registered EUDAMED B-04055207048757

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  • Withdrawn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

Generic name
Endoscope suction valve, single-use
Device name
Adapters and sealing valves
Model / Ref / Catalog
4712348, 10000201319
Description
UNIVERSAL SEALING VALVE 1-6FR for introducing instruments from 1-6Fr, PACK=5 PCS, sterile, for single use
Primary DI / UDI-DI
04055207048757
Basic UDI-DI
B-04055207048757
FDA product code
FAJ
EMDN code
A0799 Adapters, connectors, ramps, stopcocks, caps - other
GMDN term
Endoscope suction valve, single-use
Device class
Class I EUDAMED
Class II GUDID
Regulation number
876.1500
EU registration type
Legacy device (under a directive)
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class I
GUDID
Class II

Device class is stated on each registry's own scale: Class I in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Endoscope suction valve, single-use

Similar devices in this category

Other devices filed under ADAPTERS, CONNECTORS, RAMPS, STOPCOCKS, CAPS - OTHER.

Other devices from Richard Wolf GmbH

See all devices from Richard Wolf GmbH →

Properties

  • Supplied sterile
  • Single use
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (20, all answered No)