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Arthroscopic base sections

by Richard Wolf GmbH

Ref 8874.113Model 10000201422

Active European Union. Also listed in GUDID (US), not in commercial distribution.

CE MDR

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number405520705122019-0018688FQ Basic UDI-DI 04055207044568UDI-DIDate7 Nov 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number04055207044568 UDI-DI Date12 Aug 2022ListedStatusListed GUDID: not in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Generic Name
Orthopaedic fixation implant alignment tool
Device Name
Arthroscopic base sections
Model / Ref / Catalog
10000201422, 8874.113, 8874113
Description
BASE SECTION FOR STANDARD TIBIAL graduated, modular, reusable
Primary DI / UDI-DI
04055207044568
Basic UDI-DI
405520705122019-0018688FQ
Direct Marketing DI
04055207044568
FDA Product Code
NBH
EMDN Code
L1999 Arthroscopic surgery instruments, reusable - other
GMDN Term
Orthopaedic fixation implant alignment tool
Device Class
Class I
Regulation Number
888.1100
EU market of registration
Germany
GUDID distribution status
Not in Commercial Distribution
Sterilization Method
Moist Heat or Steam Sterilization

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
10000201422
8874.113
GUDID
8874113

Manufacturer details

EUDAMED SRN
DE-MF-000007048

Other devices from Richard Wolf GmbH

See all devices from Richard Wolf GmbH →

Properties

  • Premarket Exempt
  • Lot / Batch Number
  • Manufacturing Date

Other properties (21)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No