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MobileLink Acetabular Cup System 183-301/56

by WALDEMAR LINK GmbH & Co. KG

Ref 183-301/56Model Acetabular shell, TiCaP coating, uncemented, Ti6Al4V, multi hole

Expiring European Union. Also listed in GUDID (US).

CE MDR

Valid until

9 Jun 2027

CE MDR certificate

FDA recalls

None found

in data synced 24 Oct 2026

Documents

1 certificate

Certifier DNV MEDCERT GmbH

Trust

Unverified

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

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number4026575-1-HPP-103002-TJ Basic UDI-DI 04026575175963UDI-DIDate3 Jun 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number04026575175963 UDI-DI Date9 Sep 2019ListedStatusListed GUDID: in commercial distribution

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • 13690GB450220711 Expiring Amended Expires in 220 days

    Technical documentation EU MDR

    Certifier
    DNV MEDCERT GmbH 0482
    Issued
    11 Jul 2022
    Expires
    9 Jun 2027
    Reason
    Other

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 24 Oct 2026.

Coverage

2 jurisdictions

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  • Withdrawn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

Specification

EUDAMED · GUDID

Trade Name
MobileLink Acetabular Cup System
Generic Name
Acetabular shell
Model / Ref / Catalog
183-301/56, Acetabular shell, TiCaP coating, uncemented, Ti6Al4V, multi hole
Primary DI / UDI-DI
04026575175963
Basic UDI-DI
4026575-1-HPP-103002-TJ
510(k) Number
FDA Product Code
MEH, LZO, LPH, OQG
EMDN Code
P0908030302 Revision surgery uncemented acetabular cups
GMDN Term
Acetabular shell
Device Class
Class III EUDAMED
Class II GUDID
Regulation Number
888.3353, 888.3358
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class III
GUDID
Class II

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Properties

  • Sterile
  • Single Use
  • Implantable
  • Prescription Use
  • Serial Number
  • Expiration Date

Other properties (18)

  • 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
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Lot / Batch Number: No
  • Manufacturing Date: No