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Azo

by Professional Disposables International Limited United Kingdom EUDAMED

Ref AUW50FW

EMDN D0902

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number50560123TF02AZO4F Basic UDI-DIDate5 Oct 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 23 Oct 2026

Device Name
Azo® Universal Plus Dual Action
Model / Reference
AUW50FW
Primary DI / UDI-DI
05056012304976
Basic UDI-DI
50560123TF02AZO4F
Direct Marketing DI
05056012304976
EMDN Code
D0902 Associated ammonium salts for the disinfection of medical devices
Device Class
Class IIa
Market of Registration
Northern Ireland

Manufacturer details

EUDAMED SRN
GB-MF-000035214
Authorised representative
NEX MEDICAL ANTISEPTICS SRL IT-AR-000024938

Other devices from Professional Disposables International Limited

See all devices from Professional Disposables International Limited →

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED 4a8514f1-63fb-4116-b1c8-04f641eca0d7 61 fields · synced 23 Oct 2026