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Manugib 3d G T1g

EUDAMED

Class I (EU MDR)

Ref 6701-1G

by Gibaud

Identity

Trade Name
MANUGIB 3D G T1G EUDAMED
Device Name
MANUGIB 3D D T1D EUDAMED
Model / Reference
6701-1G EUDAMED

Identifiers

Primary DI / UDI-DI
03322541049674 EUDAMED
Basic UDI-DI
332254035KR EUDAMED
Direct Marketing DI
03322541049674 EUDAMED
EMDN Code
Y060612 WRIST-HAND ORTHOSES 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

Manugib 3d G T1g by Gibaud — 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
Gibaud
EUDAMED SRN
FR-MF-000014279

Sources (1)

  • EUDAMED e6eb171a-2595-4323-b75a-f60209ae8837 61 fields · synced Jul 18, 2026