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Ellipse Blanc/Rouge

EUDAMED

Class I (EU MDR)

Ref 1020082S30

by Vilgo

Identity

Trade Name
ELLIPSE BLANC/ROUGE EUDAMED
Device Name
ELLIPSE EUDAMED
Model / Reference
1020082S30 EUDAMED

Identifiers

Primary DI / UDI-DI
03615800010073 EUDAMED
Basic UDI-DI
361580ELLIPSE6M EUDAMED
Direct Marketing DI
03615800010073 EUDAMED
EMDN Code
Y12030601 ELBOW CRUTCHES 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

Ellipse Blanc/Rouge by Vilgo — 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
Vilgo
EUDAMED SRN
FR-MF-000009712

Sources (1)

  • EUDAMED d8407376-8868-4b3b-a11c-161179a775bd 61 fields · synced Jul 25, 2026