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Cryostab® Genou Universel

EUDAMED

Class I (EU MDR)

Ref CRYOSTAB® GENOU UNIVERSEL Ref CRYOSTAB® GENOU UNIVERSEL PACK

by Groupe Sober Sas

Identity

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

Identifiers

Primary DI / UDI-DI
03701459810703 EUDAMED
03701459810710 EUDAMED
Basic UDI-DI
37014598GENCRY016STFU 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 Universel 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 232635e2-6b34-468f-ba9d-1880da54aa68 61 fields · synced Jul 17, 2026
  • EUDAMED a6955107-2b1b-4205-8c61-2b81ad20cb5a 61 fields · synced May 18, 2026