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Popin's Ano/Bleu

EUDAMED

Class I (EU MDR)

Ref 1020103S02

by Vilgo

Identity

Trade Name
POPIN'S ANO/BLEU EUDAMED
Device Name
POPIN'S EUDAMED
Model / Reference
1020103S02 EUDAMED

Identifiers

Primary DI / UDI-DI
03615800052196 EUDAMED
Basic UDI-DI
361580POPINSB9 EUDAMED
Direct Marketing DI
03615800052196 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

Popin's Ano/Bleu 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 963ad610-3c7d-44a8-8a0d-9642c65be974 61 fields · synced Jul 17, 2026