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736 Lagon

EUDAMED

Class I (EU MDR)

Ref 1020010S9

by Vilgo

Identity

Trade Name
736 LAGON EUDAMED
Device Name
736 EUDAMED
Model / Reference
1020010S9 EUDAMED

Identifiers

Primary DI / UDI-DI
03615800008209 EUDAMED
Basic UDI-DI
361580736PJ EUDAMED
Direct Marketing DI
03615800008209 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

736 Lagon 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 6a5a2f72-1656-4295-936f-d3685015a13b 61 fields · synced Jul 14, 2026