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Aperlan Poka-Yoke Agent A and Agent B

by Getinge Disinfection AB FDA registration: Sweden EUDAMED

Ref 41010057 EMDN D050103

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number73401537001589 Basic UDI-DIDate28 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Aperlan Poka-Yoke Agent A and Agent B
Model / Reference
41010057
Primary DI / UDI-DI
07340153711457
Basic UDI-DI
73401537001589
EMDN Code
D050103 Peracetic acid for the disinfection of medical devices
Device Class
Class IIb
Market of Registration
Sweden

Manufacturer details

EUDAMED SRN
SE-MF-000001012

Other devices from Getinge Disinfection Ab

See all devices from Getinge Disinfection Ab →

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 703f7a98-5879-4d8a-aed2-0c872c3c41a0 61 fields · synced 24 Oct 2026