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Aniosyme Prime

by Laboratoires Anios EUDAMED

Active European Union

Ref 2367544EZ, 2367544F6, 2367544Z8, 23675445J, 2367544C2

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-03597610458644 Basic UDI-DIDate2 Sep 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  • Withdrawn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
Aniosyme Prime 12x750ml
Model / Reference
2367544EZ, 2367544F6, 2367544Z8, 23675445J, 2367544C2
Primary DI / UDI-DI
03597610458644, 03597610429224, 03597610539398, 03597610605666, 03597610579035
Basic UDI-DI
B-03597610458644, B-03597610429224, B-03597610539398, B-03597610605666, B-03597610579035
EMDN Code
D0901 Ammonium salts for the disinfection of medical devices
Device Class
Class IIa
Market of Registration
France

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