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891532040

by Richard Wolf GmbH

Ref 891532040Model 10000201182

891532040 is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 1 Sep 2026 (Basic UDI-DI B-04055207034651) and listed in FDA GUDID since 8 Aug 2024 (UDI-DI 04055207034651), 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-04055207034651 Basic UDI-DI 04055207034651UDI-DIDate1 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207034651 UDI-DI Date8 Aug 2024ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207034651 registered 1 Sep 2026 Active
  • FDA GUDID UDI-DI 04055207034651 listed 8 Aug 2024 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207034651
  2. Registered EUDAMED B-04055207034651

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  • Withdrawn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
Rigid endoscope obturator
Device name
Arthroscopic marking rods
Model / Ref / Catalog
891532040, 10000201182
Description
MARKING ROD Ø 4MM cannulated Ø 2.25 mm, PACK = 1 PC, TL 325 mm, reusable
Primary DI / UDI-DI
04055207034651
Basic UDI-DI
B-04055207034651
FDA product code
NBH
EMDN code
L031204 Arthroscopic surgery trocar, reusable
GMDN term
Rigid endoscope obturator
Device class
Class I
Regulation number
888.1100
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 — 4 Millimeter

Related devices

Category: Rigid endoscope obturator

Similar devices in this category

Other devices filed under SURGICAL TROCAR, REUSABLE.

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Properties

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