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A2301552

by Euros SAS France EUDAMED

Ref A2301552Model EUROP

EMDN P090903020201

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number37004372G0018Y Basic UDI-DIDate1 Jun 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • D1447900038 Restricted

    Technical documentation EU MDR

    Notified body
    Notified body 0483
    Issued
    22 May 2026
    Expires
    26 Nov 2028
    Reason
    Not on market

Specification

EUDAMED · synced 24 Oct 2026

Model / Reference
EUROP, A2301552
Primary DI / UDI-DI
03700437204633
Basic UDI-DI
37004372G0018Y
EMDN Code
P090903020201 Bicompartmental primary implant mobile bearing tibial inserts
Device Class
Class III
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000000605

Other devices from Euros SAS

See all devices from Euros SAS →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Implantable
Other properties (11)
  • 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

Sources (1)

  • EUDAMED 03700437204633|37004372G0018Y 61 fields · synced 24 Oct 2026