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Cryostab® Got Pack

EUDAMED

Class I (EU MDR)

Ref CRYOSTAB® GOT PACKRef CRYOSTAB® GOT

by Groupe Sober Sas

Identity

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

Identifiers

Primary DI / UDI-DI
03760035446149 EUDAMED
03760035446088 EUDAMED
03760035446132 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 Pack 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 (3)

  • EUDAMED 8e9cee69-ad5d-4435-949b-a84a7b0979b6 61 fields · synced Sep 17, 2026
  • EUDAMED f9794d7e-65b3-4665-92ae-e18702c8a51d 61 fields · synced May 19, 2026
  • EUDAMED 9de4e5a4-ff78-419a-8f4b-2bb8064bd7bd 61 fields · synced May 19, 2026