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Arthrum H 2%

by Laboratoire De Contactologie Appliquee - Lca France EUDAMED

Ref 100-2100Model ARTHRUM H 2% EMDN P900402

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-03700288620002 Basic UDI-DIDate4 Mar 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 25 Oct 2026

Device Name
ARTHRUM H 2% Boite de 1
Model / Reference
ARTHRUM H 2%, 100-2100
Primary DI / UDI-DI
03700288620002
Basic UDI-DI
B-03700288620002
EMDN Code
P900402 Resorbable filling and reconstruction devices
Device Class
Class III
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000001732

Other devices from Laboratoire De Contactologie Appliquee - Lca

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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 03700288620002|B-03700288620002 61 fields · synced 25 Oct 2026