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Cryostab® Poignet

EUDAMED

Class I (EU MDR)

Ref CRYOSTAB® POIGNET

by Groupe Sober Sas

Identity

Trade Name
CRYOSTAB® POIGNET EUDAMED
Device Name
CRYOSTAB® POIGNET EUDAMED
Model / Reference
CRYOSTAB® POIGNET EUDAMED

Identifiers

Primary DI / UDI-DI
03760035448662 EUDAMED
Basic UDI-DI
376003544POICRY004STRE 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

Cryostab® Poignet 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 e50a968b-9217-4ebc-8574-1a921aa15e50 61 fields · synced Jun 18, 2026