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Cemented Acetabular Cup System

by Waldemar Link GmbH & Co. KG 232 variants

Ref 101-134Model Acetabular cup, cemented, UHMWPE, CoCrNiMoFe, without snap-fit, eccentric

Active European Union

CE MDR

Valid until

23 May 2029

CE MDR certificate

FDA recalls

Not applicable

No FDA record for this device

Documents

1 certificate

Certifier DNV MEDCERT GmbH

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4026575-1-HPP-102004-TD Basic UDI-DI 04026575197019UDI-DIDate28 May 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 13785GB450240524 Active

    Technical documentation EU MDR

    Certifier
    DNV MEDCERT GmbH 0482
    Issued
    24 May 2024
    Expires
    23 May 2029

Coverage

1 jurisdiction

Germany
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

  • Germany

Specification

EUDAMED

Device Name
Cemented Acetabular Cup System
Model / Reference
Acetabular cup, cemented, UHMWPE, CoCrNiMoFe, without snap-fit, eccentric, 101-134
Primary DI / UDI-DI
04026575197019
Basic UDI-DI
4026575-1-HPP-102004-TD
EMDN Code
P090803010102 Primary implant cemented polyethylene acetabular cups, one-piece
Device Class
Class III
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005215

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Properties

  • Sterile
  • Implantable
  • CMR Substance

Other properties (10)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No