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08056304411341

by Adranox SRL Italy EUDAMED

Ref ADMR101.10

EMDN D050199

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number805630441LYSONOX---PPAAPD Basic UDI-DIDate30 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

Device Name
Lysonox Pulver Paa
Model / Reference
ADMR101.10
Primary DI / UDI-DI
08056304411341
Basic UDI-DI
805630441LYSONOX---PPAAPD
Unit of Use DI
08056304411358
EMDN Code
D050199 Associated peracetic acid for the disinfection of medical devices - other
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 4bba5d30-fbf2-45d7-b47b-89eb438a1a60 61 fields · synced 22 Oct 2026