← Back to catalogue

Cryostab® Got

EUDAMED

Class I (EU MDR)

Ref CRYOSTAB® GOT

by Groupe Sober Sas

Identity

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

Identifiers

Primary DI / UDI-DI
03760035446071 EUDAMED
Basic UDI-DI
376003544THOCRY001STSS EUDAMED
EMDN Code
Y0699 EXTERNAL PROSTHESES AND ORTHOSES - OTHER 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® Got 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 9cf21a30-a006-4ec3-8c61-5bc4c7aa9b36 61 fields · synced Jun 18, 2026