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Cryostab® 10 En 1

EUDAMED

Class I (EU MDR)

Ref CRYOSTAB® 10 EN 1

by Groupe Sober Sas

Identity

Trade Name
CRYOSTAB® 10 EN 1 EUDAMED
Device Name
CRYOSTAB® 10 EN 1 EUDAMED
Model / Reference
CRYOSTAB® 10 EN 1 EUDAMED

Identifiers

Primary DI / UDI-DI
03701459810628 EUDAMED
Basic UDI-DI
37014598TECCRY003STKU EUDAMED
EMDN Code
M030504 IMMOBILISATION SYSTEMS, MOULDABLE UNDER COLD AND HOT TEMPERATURES 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® 10 En 1 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 (1)

  • EUDAMED cd6740e9-f77f-4154-bba7-42fd329b2d70 61 fields · synced Jul 31, 2026