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Cryostab® Cheville Pack

EUDAMED

Class I (EU MDR)

Ref CRYOSTAB® CHEVILLE PACKModel CRYOSTAB® CHEVILLE

by Groupe Sober Sas

Identity

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

Identifiers

Primary DI / UDI-DI
03701459809530 EUDAMED
03701459809516 EUDAMED
Basic UDI-DI
376003544CHECRY001ST35 EUDAMED
EMDN Code
Y06120601 PASSIVE ANKLE-FOOT 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

Category: Ankle/foot orthosis

Cryostab® Cheville Pack by Groupe Sober Sas — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Ankle/foot orthosis.

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 d195ed5b-3960-462c-b446-84edacef66db 61 fields · synced Jul 28, 2026
  • EUDAMED cc299a5b-50b2-44eb-aad3-d5f5d8f19261 61 fields · synced May 16, 2026