Skip to content

Set De Pose De Kt a

by Hemodia SAS 3 variants

Ref 9785_1

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 linked in EUDAMED

A group certificate may exist

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 Number3661379ASS33ANE2AHZ Basic UDI-DI 03661379263112UDI-DIDate21 May 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Assemblage ANESTHESIE-REANIMATION STE
Model / Reference
9785_1
Primary DI / UDI-DI
03661379263112
Basic UDI-DI
3661379ASS33ANE2AHZ
EMDN Code
A030499 Administration kits - other
Device Class
Class IIa
Medical Purpose
Les assemblages de la gamme ‘Anesthésie-réanimation’ sont destinés à : Être utilisés pour les anesthésies loco-régionales et la pose/retrait de voies veineuses centrales, périphériques type MidLine, périnerveuses et pour la gestion de la douleur

Manufacturer details

EUDAMED SRN
FR-PR-000007189

Other devices from Hemodia SAS

See all devices from Hemodia SAS →

Properties

  • Sterile