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Genouillere Rotulig T5

EUDAMED

Class I (EU MDR)

Ref GE0112BI5

by Orliman, S.L.U.

Identity

Trade Name
GENOUILLERE ROTULIG T5 EUDAMED
Device Name
GENOUILLERE EUDAMED
Model / Reference
GE0112BI5 EUDAMED

Identifiers

Primary DI / UDI-DI
08435025925779 EUDAMED
Basic UDI-DI
84350259ORLSM204014C 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

Yes

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

Genouillere Rotulig T5 by Orliman, S.L.U. — 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

Manufacturer
Orliman, S.L.U.
EUDAMED SRN
ES-MF-000001598

Sources (1)

  • EUDAMED d38fd3c1-2316-4c5a-a7d6-9b5351d2cdaf 61 fields · synced Jul 19, 2026