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Single Axis Foot Two Hole with Adapter Size 28 Right

by Roadrunnerfoot Engineering srl

Ref 1.007.02.28RModel SIZE 22,23,24,25,26,27,28,29 SIDE RIGHT/LEFT

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 Number8055748721.007.02G9 Basic UDI-DI 08055748721474UDI-DIDate30 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  • Withdrawn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
Single Axis Foot Two Hole with Adapter
Model / Reference
SIZE 22, 23, 24, 25, 26, 27, 28, 29 SIDE RIGHT/LEFT, 1.007.02.28R
Primary DI / UDI-DI
08055748721474
Basic UDI-DI
8055748721.007.02G9
EMDN Code
Y062499 Lower extremity prostheses - other
Device Class
Class I
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000008242

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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