Skip to content

Marathon XLPE

by DePuy Ireland UC Ireland EUDAMED

Ref 9655-12-238Model MARATHON XLPE Cemented Cup EMDN P090803010102,P0908030301

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0603295a0021083 Basic UDI-DIDate27 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • MDR 755949 Supplemented

    Technical documentation EU MDR

    Notified body
    Notified body 2797
    Issued
    30 Jun 2026
    Expires
    12 Oct 2027
    Reason
    Change approved

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Cemented Cup
Model / Reference
MARATHON XLPE Cemented Cup, 9655-12-238
Primary DI / UDI-DI
10603295330097
Basic UDI-DI
0603295a0021083
EMDN Code
P090803010102,P0908030301
Device Class
Class III
Market of Registration
Ireland

Manufacturer details

EUDAMED SRN
IE-MF-000007377

Other devices from DePuy Ireland UC

See all devices from DePuy Ireland UC →

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 10603295330097|0603295A0021083 61 fields · synced 24 Oct 2026