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ENFORCE Active Foot

by ENforce Medical Technologies Sp. z o.o. 4 variants

Ref EAF55Model EAF13,EAF14,EAF15,EAF33,EAF34,EAF35,EAF53,EAF54,EAF55,EAF63,EAF64,EAF65

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number59054969507ACTIVEFOOT75 Basic UDI-DI 05906952972196UDI-DIDate14 Feb 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  • Withdrawn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

Model / Reference
EAF13, EAF14, EAF15, EAF33, EAF34, EAF35, EAF53, EAF54, EAF55, EAF63, EAF64, EAF65
Primary DI / UDI-DI
05906952972196
Basic UDI-DI
59054969507ACTIVEFOOT75
Direct Marketing DI
05906952972196
EMDN Code
Y062403 Foot partial prostheses (including toe prostheses)
Device Class
Class I
EU market of registration
Poland

Manufacturer details

EUDAMED SRN
PL-MF-000043797

Other devices from ENforce Medical Technologies Sp. z o.o.

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