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8243901

by Richard Wolf GmbH

Ref 8243.901Model 10000201241

8243901 (8243.901) is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 5 Oct 2026 (Basic UDI-DI B-04055207041819) and listed in FDA GUDID since 21 May 2024 (UDI-DI 04055207041819), 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-04055207041819 Basic UDI-DI 04055207041819UDI-DIDate5 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207041819 UDI-DI Date21 May 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207041819 registered 5 Oct 2026 Active
  • FDA GUDID UDI-DI 04055207041819 listed 21 May 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207041819
  2. Registered EUDAMED B-04055207041819

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  • Withdrawn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, 8243.901, 8243901
Description
PROBE Ø 5.0MM WL 450MM 450 mm WL, d=7 mm
Primary DI / UDI-DI
04055207041819
Basic UDI-DI
B-04055207041819
FDA product code
FGM
EMDN code
L1216 Laparoscopic and thoracoscopic surgery palpators, reusable
GMDN term
Endoscopic surgical probe
Device class
Class I
Regulation number
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
Size
Outer Diameter — 5.0 Millimeter
Length — 450 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
10000201241
8243.901
GUDID
8243901

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)