← Back to catalogue

Genouillere Rotulig T Enf

EUDAMED

Class I (EU MDR)

Ref GE0112BI0

by Orliman, S.L.U.

Identity

Trade Name
GENOUILLERE ROTULIG T ENF EUDAMED
Device Name
GENOUILLERE EUDAMED
Model / Reference
GE0112BI0 EUDAMED

Identifiers

Primary DI / UDI-DI
08435025925557 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 T Enf 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

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

Sources (1)

  • EUDAMED 20a3d743-f2f9-48b5-b4b1-bddf203ce608 61 fields · synced Jul 20, 2026