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Kartilage® Cross

by Laboratoires Vivacy France EUDAMED

Ref SPF040Model INTRA ARTICULAR

EMDN P900402

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-SPF040G8 Basic UDI-DIDate3 Apr 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/MDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Kartilage® Cross
Model / Reference
INTRA ARTICULAR, SPF040
Primary DI / UDI-DI
D-SPF040G8
Basic UDI-DI
B-SPF040G8
EMDN Code
P900402 Resorbable filling and reconstruction devices
Device Class
Class III
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000003771

Other devices from Laboratoires Vivacy

See all devices from Laboratoires Vivacy →

Properties & raw data

Show properties, registry sources and raw records
  • Sterile
  • Implantable
Other properties (9)
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No

Sources (1)

  • EUDAMED 9f3accba-9658-46b5-a78b-48e737d3a93c 61 fields · synced 22 Oct 2026