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Roadflexion Foot Hp Size V-Long Soft

by Roadrunnerfoot Engineering srl

Ref 1.002.02.V-LONG.SModel SIZE I,II,III,IV,V,V-LONG,VI CATEGORY SOFT/HARD

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number8055748721.002.02F6 Basic UDI-DI 08053608454692UDI-DIDate29 Jun 2025RegisteredStatusActive

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  • Withdrawn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

Device Name
Roadflexion Hp
Model / Reference
SIZE I, II, III, IV, V, V-LONG, VI CATEGORY SOFT/HARD, 1.002.02.V-LONG.S
Primary DI / UDI-DI
08053608454692
Basic UDI-DI
8055748721.002.02F6
EMDN Code
Y062499 Lower extremity prostheses - other
Device Class
Class I
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000008242

Other devices from Roadrunnerfoot Engineering srl

See all devices from Roadrunnerfoot Engineering srl →

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