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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
03760035448679 EUDAMED
03760035448655 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 (2)

  • EUDAMED a6936e32-d434-40b1-befb-121611188bd2 61 fields · synced Jul 30, 2026
  • EUDAMED 96760fff-f1ff-46cd-b9bf-660dae7bf3ec 61 fields · synced May 19, 2026