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Genupro Control

EUDAMED

Class I (EU MDR)

Ref T39100120305502

by Thuasne Deutschland GmbH

Identity

Device Name
GENUPRO CONTROL EUDAMED
Model / Reference
T39100120305502 EUDAMED

Identifiers

Primary DI / UDI-DI
04035459333115 EUDAMED
Basic UDI-DI
4035459DE0804A49 EUDAMED
Direct Marketing DI
04035459333115 EUDAMED
EMDN Code
Y061209 KNEE ORTHOSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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

Genupro Control by Thuasne Deutschland GmbH — 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-000006210

Sources (1)

  • EUDAMED 863ae66c-88a3-4fc6-88bf-6015af2fb981 61 fields · synced Jun 18, 2026