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Orthopus

by Orthopus France EUDAMED

Ref 1002

EMDN Y241899

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number37700264781002NQ Basic UDI-DIDate23 Sep 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
ORTHOPUS Partner
Model / Reference
1002
Primary DI / UDI-DI
03770026478011
Basic UDI-DI
37700264781002NQ
EMDN Code
Y241899 Arm, hand, finger function aid and/or substitution devices - other
Device Class
Class I
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000037107

Other devices from Orthopus

Properties & raw data

Show properties, registry sources and raw records
Other properties (13)
  • Sterile: No
  • Implantable: No
  • 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 88f71134-0abc-4993-bcae-1d804c320150 61 fields · synced 22 Oct 2026