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Stabigast Femme - T10

by Groupe Sober SAS

Ref STABIGAST FEMMEModel CEINTURE ABDOMINALE EPIGASTRIQUE

Active European Union

CE MDD

Valid until

Not listed

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

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-03701459809165 Basic UDI-DI 03701459809165UDI-DIDate24 Jul 2026RegisteredStatusActive

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  • Withdrawn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/MDD Active

Specification

EUDAMED

Device Name
Stabigast Femme
Model / Reference
CEINTURE ABDOMINALE EPIGASTRIQUE, STABIGAST FEMME
Primary DI / UDI-DI
03701459809165
Basic UDI-DI
B-03701459809165
EMDN Code
Y060307 Thoracic orthoses
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000017818

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See all devices from Groupe Sober SAS →

Properties

Other properties (11)

  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No