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Cryostab® Patella Pack

EUDAMED

Class I (EU MDR)

Ref CRYOSTAB® PATELLA PACKModel CRYOSTAB® PATELLA

by Groupe Sober Sas

Identity

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

Identifiers

Primary DI / UDI-DI
03701459809691 EUDAMED
03701459809684 EUDAMED
Basic UDI-DI
37014598GENCRY010STEW 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® Patella 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 51104d69-b98c-4dc2-81b7-0f52b2c93726 61 fields · synced Jul 15, 2026
  • EUDAMED 33ad1bbc-2f74-4821-a8da-c30186019c02 61 fields · synced May 18, 2026