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891510012

by Richard Wolf GmbH

Ref 891510012Model 10000201131

891510012 is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 7 Oct 2026 (Basic UDI-DI B-04055207034637) and listed in FDA GUDID since 3 Aug 2022 (UDI-DI 04055207034637), 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-04055207034637 Basic UDI-DI 04055207034637UDI-DIDate7 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207034637 UDI-DI Date3 Aug 2022ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207034637 registered 7 Oct 2026 Active
  • FDA GUDID UDI-DI 04055207034637 listed 3 Aug 2022 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207034637
  2. Registered EUDAMED B-04055207034637

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  • Withdrawn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
Arthroscopic tunnel probes
Model / Ref / Catalog
891510012, 10000201131
Description
TUNNEL PROBE WL 140MM graduated, reusable
Primary DI / UDI-DI
04055207034637
Basic UDI-DI
B-04055207034637
FDA product code
NBH
EMDN code
L1999 Arthroscopic surgery instruments, reusable - other
GMDN term
Endoscopic surgical probe
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
Length — 140 Millimeter

Related devices

Category: Endoscopic surgical probe

Similar devices in this category

Other devices filed under ARTHROSCOPIC SURGERY INSTRUMENTS, REUSABLE - OTHER.

Other devices from Richard Wolf GmbH

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Properties

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