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Pallas Ano/Fuchsia

EUDAMED

Class I (EU MDR)

Ref 1020102S02

by Vilgo

Identity

Trade Name
PALLAS ANO/FUCHSIA EUDAMED
Device Name
PALLAS ANO EUDAMED
Model / Reference
1020102S02 EUDAMED

Identifiers

Primary DI / UDI-DI
03615800045976 EUDAMED
Basic UDI-DI
361580PALLASANOGC EUDAMED
Direct Marketing DI
03615800045976 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

Pallas Ano/Fuchsia 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 39d015d7-39a7-470c-9564-fd87628fac33 61 fields · synced Jul 26, 2026