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Aniospray Quick

by Laboratoires Anios EUDAMED

Active European Union

Ref 2084073Z8, 2084073OB, 2084073AB, 2084225E2

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-03597610539275 Basic UDI-DIDate6 May 2025RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED

Device Name
Aniospray Quick 12x1L
Model / Reference
2084073Z8, 2084073OB, 2084073AB, 2084225E2
Primary DI / UDI-DI
03597610539275, 03597610195594, 03597610647086, 03597610529375
Basic UDI-DI
B-03597610539275, B-03597610195594, B-03597610647086, B-03597610529375
EMDN Code
D0701 Ethanol for the disinfection of medical devices
Device Class
Class IIa
Market of Registration
Türkiye
France
Bulgaria
Spain

Manufacturer details

EUDAMED SRN
FR-MF-000011756

Other devices from Laboratoires Anios

See all devices from Laboratoires Anios →

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