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AQUISFEK SAF 3, 3 mL

by Aquisel S.L.U. EUDAMED

Active European Union

Ref 1800505Model AQUISEL AQUISFEK

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number8429889-TF-4000-MQ Basic UDI-DIDate16 Jun 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/IVDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Aquisfek
Model / Reference
AQUISEL AQUISFEK, 1800505
Primary DI / UDI-DI
08429889002233
Market of Registration
Spain

Manufacturer details

EUDAMED SRN
ES-MF-000020750

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