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Revitan®

by Zimmer Switzerland Manufacturing GmbH EUDAMED

Active European Union

Ref 01.00409.636

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number889024ZAKY Basic UDI-DIDate20 Oct 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

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.

Specification

EUDAMED

Device Name
Revitan®, rasp, distal, curved
Model / Reference
01.00409.636
Primary DI / UDI-DI
00889024532090
Basic UDI-DI
889024ZAKY
Direct Marketing DI
00889024532090
EMDN Code
L091104 Orthopaedic prostheses positioners, reusable
Device Class
Class IIa
Market of Registration
Netherlands

Manufacturer details

EUDAMED SRN
CH-MF-000008793
Authorised representative
Biomet Global Supply Chain Center B.V. NL-AR-000000422

Other devices from Zimmer Switzerland Manufacturing GmbH

See all devices from Zimmer Switzerland Manufacturing GmbH →

Properties

  • CMR Substance

Other properties (12)

  • Sterile: No
  • Implantable: No
  • 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