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Lysonox Paa

by Adranox SRL Italy EUDAMED

Ref ADMR102.50Model ADMR102.10

EMDN S9002

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805630441LYSONOX----PAAFX Basic UDI-DIDate29 Nov 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Model / Reference
ADMR102.10, ADMR102.50
Primary DI / UDI-DI
08056304411396
Basic UDI-DI
805630441LYSONOX----PAAFX
Unit of Use DI
08056304411556
EMDN Code
S9002 Devices for sterilisation with peracetic acid (excluding cat. d - z)
Device Class
Class IIb
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000027181

Other devices from Adranox SRL

See all devices from Adranox SRL →

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 6b0dfdbf-0bad-4ec9-be39-62249dd4b0af 61 fields · synced 22 Oct 2026