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Cryostab® Gac

EUDAMED

Class I (EU MDR)

Ref CRYOSTAB® GAC

by Groupe Sober Sas

Identity

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

Identifiers

Primary DI / UDI-DI
03760035441946 EUDAMED
Basic UDI-DI
376003544GENCRY003STB3 EUDAMED
EMDN Code
Y061209 KNEE 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® Gac 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 6b95b336-c670-428f-81fa-65393a354f0f 61 fields · synced Jun 18, 2026