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Cryostab Compresse

by Groupe Sober SAS

Ref CRYOSTAB COMPRESSEModel COMPRESSE DE FROID

Cryostab Compresse is a Class I device made by Groupe Sober SAS, registered in EUDAMED on 15 Jul 2026 (Basic UDI-DI 3701459811AXDV-GE000QJ), active as of 25 Oct 2026.

Active European Union

CE MDR

Valid until

No date given

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Source EUDAMED, synced 25 Oct 2026.

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3701459811AXDV-GE000QJ Basic UDI-DI Date15 Jul 2026RegisteredStatusActive

Official records

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Model / reference
COMPRESSE DE FROID, CRYOSTAB COMPRESSE
Primary DI / UDI-DI
03701459811632, 03701459811625, 03701459811649, 03701459811656
Basic UDI-DI
3701459811AXDV-GE000QJ
EMDN code
M9001 Cryotherapy and thermotherapy devices
Device class
Class I
System or procedure pack
Procedure pack which is a device in itself
EU registration type
Standard device
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000017818

Similar devices in this category

Other devices filed under CRYOTHERAPY AND THERMOTHERAPY DEVICES.

Other devices from Groupe Sober SAS

See all devices from Groupe Sober SAS →

Properties

Other properties (14, all answered No)