← Back to catalogue

Cryostab® Rack

EUDAMED

Class I (EU MDR)

Ref CRYOSTAB® RACK

by Groupe Sober Sas

Identity

Trade Name
CRYOSTAB® RACK EUDAMED
Device Name
CRYOSTAB® RACK EUDAMED
Model / Reference
CRYOSTAB® RACK EUDAMED

Identifiers

Primary DI / UDI-DI
03760035445500 EUDAMED
03760035445739 EUDAMED
Basic UDI-DI
376003544TECFRO003STDG EUDAMED
EMDN Code
M9001 CRYOTHERAPY AND THERMOTHERAPY DEVICES 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® Rack 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Groupe Sober Sas
EUDAMED SRN
FR-MF-000017818

Sources (2)

  • EUDAMED d6012380-a492-4647-8066-e327416c433f 61 fields · synced Jul 11, 2026
  • EUDAMED 88a000f8-765d-4660-8615-af408fad65b0 61 fields · synced May 19, 2026