Skip to content

8379672

by Richard Wolf GmbH

Ref 8379.672Model 10000201241

8379672 (8379.672) is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 5 Oct 2026 (Basic UDI-DI B-04055207014967) and listed in FDA GUDID since 19 Aug 2024 (UDI-DI 04055207014967), active as of 25 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 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-04055207014967 Basic UDI-DI 04055207014967UDI-DIDate5 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207014967 UDI-DI Date19 Aug 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207014967 registered 5 Oct 2026 Active
  • FDA GUDID UDI-DI 04055207014967 listed 19 Aug 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207014967
  2. Registered EUDAMED B-04055207014967

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  • Withdrawn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
Endoscopic surgical probe
Device name
Surgical laparoscopic probes
Model / Ref / Catalog
10000201241, 8379.672, 8379672
Description
PROBE 3.5MM WL 250MM graduated, reusable
Primary DI / UDI-DI
04055207014967
Basic UDI-DI
B-04055207014967
FDA product code
NWV, FGM
EMDN code
L1216 Laparoscopic and thoracoscopic surgery palpators, reusable
GMDN term
Endoscopic surgical probe
Device class
Class I
Regulation number
884.1720, 876.4730
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

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
10000201241
8379.672
GUDID
8379672

Related devices

Category: Endoscopic surgical probe

Similar devices in this category

Other devices filed under LAPAROSCOPIC AND THORACOSCOPIC SURGERY INSTRUMENTS, REUSABLE.

Other devices from Richard Wolf GmbH

See all devices from Richard Wolf GmbH →

Properties

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