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Genouillere Rotulig T2

EUDAMED

Class I (EU MDR)

Ref GE0112BI2

by Orliman, S.L.U.

Identity

Trade Name
GENOUILLERE ROTULIG T2 EUDAMED
Device Name
GENOUILLERE EUDAMED
Model / Reference
GE0112BI2 EUDAMED

Identifiers

Primary DI / UDI-DI
08435025925588 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 T2 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 5f9ac5a3-db6b-4b75-836b-7751ade310b4 61 fields · synced Jul 18, 2026