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Vario-Cup System

by Waldemar Link GmbH & Co. KG 6 variants

Ref 99-0055/48Model Bipolar head, uncemented, CoCrMo, UHMWPE

Active European Union

CE MDR

Valid until

9 Jul 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 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number4026575-1-HSP-034001-X7 Basic UDI-DI 04026575352845UDI-DIDate12 May 2026RegisteredStatusActive

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 13794GB450240710 Active

    Technical documentation EU MDR

    Certifier
    DNV MEDCERT GmbH 0482
    Issued
    10 Jul 2024
    Expires
    9 Jul 2029

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Vario-Cup System
Model / Reference
Bipolar head, uncemented, CoCrMo, UHMWPE, 99-0055/48
Primary DI / UDI-DI
04026575352845
Basic UDI-DI
4026575-1-HSP-034001-X7
EMDN Code
P0908040503 Hip prostheses, bi-articular cups
Device Class
Class III
EU market of registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000005215

Other devices from Waldemar Link GmbH & Co. KG

See all devices from Waldemar Link GmbH & Co. KG →

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