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"ambi Plateform"

EUDAMED

Class I (EU MDR)

Ref AMBI PLATEFORMModel Attelle de poignet-main-doigts

by Groupe Sober Sas

Identity

Trade Name
"AMBI PLATEFORM" EUDAMED
Device Name
AMBI PLATEFORM EUDAMED
Model / Reference
Attelle de poignet-main-doigts EUDAMED
AMBI PLATEFORM EUDAMED

Identifiers

Primary DI / UDI-DI
03701459810611 EUDAMED
Basic UDI-DI
37014598POIIMM031STRQ EUDAMED
EMDN Code
Y060613 WRIST-HAND-FINGERS 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

"ambi Plateform" by Groupe Sober Sas — 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
Groupe Sober Sas
EUDAMED SRN
FR-MF-000017818

Sources (1)

  • EUDAMED 1575c092-ed0d-4807-8eed-d8e79854afaa 61 fields · synced Aug 4, 2026