Skip to content

SMARTLEG Transparent classe 2 bas autofixant taille 2+ normal Ravissante pieds ouverts

by Laboratoires INNOTHERA

Ref 3664540053789

Active European Union

CE MDR

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number3664540CVECL2ASQDT02YB Basic UDI-DI 03664540053789UDI-DIDate22 Aug 2025RegisteredStatusActive

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  • Withdrawn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

Device Name
Produit de compression veineuse élastique de classe 2
Model / Reference
3664540053789
Primary DI / UDI-DI
03664540053789
Basic UDI-DI
3664540CVECL2ASQDT02YB
EMDN Code
M030405 Compression stockings
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000004678

Other devices from Laboratoires INNOTHERA

See all devices from Laboratoires INNOTHERA →

Properties

Other properties (13)

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