← Back to catalogue

Cryostab Pack Genou

EUDAMED

Class I (EU MDR)

Ref CRYOSTAB PACK GENOUModel CRYOSTAB COMBO

by Groupe Sober Sas

Identity

Trade Name
CRYOSTAB PACK GENOU EUDAMED
Device Name
CRYOSTAB COMBO EUDAMED
Model / Reference
CRYOSTAB COMBO EUDAMED
CRYOSTAB PACK GENOU EUDAMED

Identifiers

Primary DI / UDI-DI
03701459810789 EUDAMED
Basic UDI-DI
37014598TECCRY004STKZ EUDAMED
EMDN Code
M030504 IMMOBILISATION SYSTEMS, MOULDABLE UNDER COLD AND HOT TEMPERATURES 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 Pack Genou 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Groupe Sober Sas
EUDAMED SRN
FR-MF-000017818

Sources (1)

  • EUDAMED d8bd36b8-258e-4efe-844e-4e6957697cef 61 fields · synced Jun 19, 2026