← Back to catalogue

Hallux Valgus Ecarteur De Doigt Tm (vendu Par 2)

EUDAMED

Class I (EU MDR)

Ref CP06132UM

by Orliman, S.L.U.

Identity

Trade Name
HALLUX VALGUS ECARTEUR DE DOIGT TM (VENDU PAR 2) EUDAMED
Device Name
PODOLOGIE EUDAMED
Model / Reference
CP06132UM EUDAMED

Identifiers

Primary DI / UDI-DI
08435025907850 EUDAMED
Basic UDI-DI
84350259ORLSM204184V EUDAMED
EMDN Code
Y061203 ORTHOSES, FOOT (INCLUDING INSOLES AND INSERTS) 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

Hallux Valgus Ecarteur De Doigt Tm (vendu Par 2) 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 72a016fe-7660-4512-9a07-94a978f02260 61 fields · synced Oct 6, 2026