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Cryostab® Genou Pack

EUDAMED

Class I (EU MDR)

Ref CRYOSTAB® GENOU PACKModel CRYOSTAB® GENOU

by Groupe Sober Sas

Identity

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

Identifiers

Primary DI / UDI-DI
03701459810840 EUDAMED
03760035445609 EUDAMED
Basic UDI-DI
376003544GENCRY001STA55 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® Genou 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 (2)

  • EUDAMED ea441f0a-9d97-40f5-ba0e-d95b32fdc21b 61 fields · synced Sep 18, 2026
  • EUDAMED cd3b0b34-5ffd-4e10-926d-90b53a96cd3a 61 fields · synced May 19, 2026