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8866951

by Richard Wolf GmbH

Ref 8866.951Model 10000201166

8866951 (8866.951) is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 6 Oct 2026 (Basic UDI-DI B-04055207021194) and listed in FDA GUDID since 20 Mar 2025 (UDI-DI 04055207021194), active as of 24 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 24 Oct 2026.

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED NumberB-04055207021194 Basic UDI-DI 04055207021194UDI-DIDate6 Oct 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207021194 UDI-DI Date20 Mar 2025ListedStatusListed GUDID: in commercial distribution

Official records

Across registries

2 registries list this device

  • EUDAMED Basic UDI-DI B-04055207021194 registered 6 Oct 2026 Active
  • FDA GUDID UDI-DI 04055207021194 listed 20 Mar 2025 Listed

Timeline

2 dated events

  1. Listed FDA GUDID 04055207021194
  2. Registered EUDAMED B-04055207021194

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  • Withdrawn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
Tendon stripper
Device name
Arthroscopic tendon strippers
Model / Ref / Catalog
10000201166, 8866.951, 8866951
Description
TENDON STRIPPER UNIVERSAL 300MM SZ 8MM by Pässler, dull, graduated, take-apart, reusable
Primary DI / UDI-DI
04055207021194
Basic UDI-DI
B-04055207021194
FDA product code
HRT
EMDN code
L1999 Arthroscopic surgery instruments, reusable - other
GMDN term
Tendon stripper
Device class
Class I
Regulation number
888.4540
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 — 300.0 Millimeter

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / referenceEUDAMED
10000201166
8866.951
GUDID
8866951

Related devices

Category: Tendon stripper

Similar devices in this category

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

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)