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Prothesenfüße

EUDAMED

Class I (EU MDR)

Ref 46.031.800.202.026

by Uniprox GmbH & Co.KG

Identity

Device Name
Prothesenfüße EUDAMED
Model / Reference
46.031.800.202.026 EUDAMED

Identifiers

Primary DI / UDI-DI
04053646070940 EUDAMED
Basic UDI-DI
4053646Feet7N EUDAMED
EMDN Code
Y062403 FOOT PARTIAL PROSTHESES (INCLUDING TOE PROSTHESES) EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prothesenfüße by Uniprox Gmbh & Co. Kg — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
DE-MF-000010327

Sources (1)

  • EUDAMED 6ccaa2fc-9b13-411a-a85d-c27e43231f33 61 fields · synced Jul 8, 2026