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Stabilight 20°

by Groupe Sober SAS

Ref STABILIGHT 20°Model ATTELLE DE GENOU AJOUREE FLEXION

Stabilight 20° is a Class I device made by Groupe Sober SAS, registered in EUDAMED on 22 Jul 2026 (Basic UDI-DI B-03760035444947), active as of 25 Oct 2026.

Active European Union

CE MDD

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/MDD NumberB-03760035444947 Basic UDI-DI Date22 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  • Withdrawn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/MDD Active

Specification

EUDAMED

Model / reference
ATTELLE DE GENOU AJOUREE FLEXION, STABILIGHT 20°
Primary DI / UDI-DI
03760035444947, 03760035444961, 03760035444954, 03760035444978
Basic UDI-DI
B-03760035444947, B-03760035444961, B-03760035444954, B-03760035444978
EMDN code
Y061209 Knee orthoses
Device class
Class I
System or procedure pack
System which is a device in itself
EU registration type
Legacy device (under a directive)
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000017818

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Properties

Other properties (12, all answered No)