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Pied prothétique polyarticulé Upya By Exoneo P5 Droit Clair

by Exoneo

Ref 01CDC1-P5, 01CDC1-P5-TC

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number37700158050194 Basic UDI-DI Date30 Nov 2021RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Trade Name
Pied prothétique polyarticulé Upya By Exoneo P5 Droit Clair
Pied Prothétique polyarticulé Upya by Exoneo P5 Droit Clair Tissu Carbone
Device Name
Upya
Model / Reference
01CDC1-P5, 01CDC1-P5-TC
Primary DI / UDI-DI
37700158050646, 37700158052176
Basic UDI-DI
37700158050194
EMDN Code
Y062403, Y062409
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000003061

Other devices from Exoneo

See all devices from Exoneo →

Properties

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