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Cryostab Cast Pack

EUDAMED

Class I (EU MDR)

Ref CRYOSTAB CAST PACKModel CRYOSTAB CAST

by Groupe Sober Sas

Identity

Trade Name
CRYOSTAB CAST PACK EUDAMED
Device Name
CRYOSTAB CAST EUDAMED
Model / Reference
CRYOSTAB CAST EUDAMED
CRYOSTAB CAST PACK EUDAMED

Identifiers

Primary DI / UDI-DI
03701459811021 EUDAMED
Basic UDI-DI
37014598PIECRY011STLX 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 Cast 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 (1)

  • EUDAMED cd810e4c-3c1f-4486-971d-7df7e30774d3 61 fields · synced Jun 19, 2026