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Stabipouce Ambi

EUDAMED

Class I (EU MDR)

Ref STABIPOUCE AMBI

by Groupe Sober Sas

Identity

Trade Name
STABIPOUCE AMBI EUDAMED
Device Name
STABIPOUCE AMBI EUDAMED
Model / Reference
STABIPOUCE AMBI EUDAMED

Identifiers

Primary DI / UDI-DI
03701459810673 EUDAMED
Basic UDI-DI
37014598POPIMM003STWE 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

Stabipouce Ambi 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 d68e9b4e-8611-43a7-9c7c-023dbe3fb199 61 fields · synced Jul 10, 2026