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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
03760035441953 EUDAMED
03760035441939 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 (2)

  • EUDAMED bdb2fd15-e9d4-42e0-bc6e-d56e18b7ea0e 61 fields · synced Jul 18, 2026
  • EUDAMED 78aab1c9-ddb3-4316-a8fe-eb17ca34f6cc 61 fields · synced May 19, 2026