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726 - Gt 840/1115

EUDAMED

Class I (EU MDR)

Ref 1020006S2Ref 1020006S3

by Vilgo

Identity

Trade Name
726 - GT 840/1115 EUDAMED
726 - GT 840/1115 rallonge haute 761 EUDAMED
Device Name
726 EUDAMED
Model / Reference
1020006S2 EUDAMED
1020006S3 EUDAMED

Identifiers

Primary DI / UDI-DI
03615800000074 EUDAMED
03615800053155 EUDAMED
Basic UDI-DI
361580726PF EUDAMED
Direct Marketing DI
03615800000074 EUDAMED
03615800053155 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

726 - Gt 840/1115 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 (2)

  • EUDAMED 9230d35e-a701-4e09-85d4-548f38b25957 61 fields · synced Jul 29, 2026
  • EUDAMED 3eb8886a-6d61-45a5-8dfa-fbdc113c9e3b 61 fields · synced May 18, 2026