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UMONIUM38® Neutralis 5L

by Laboratoire Huckert's International Belgium EUDAMED

Ref PF12512 EMDN D0901

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-05425037714129 Basic UDI-DIDate19 Apr 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  • Withdrawn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 · synced 22 Oct 2026

Device Name
UMONIMU38® Neutralis 5L
Model / Reference
PF12512
Primary DI / UDI-DI
05425037714129
Basic UDI-DI
B-05425037714129
EMDN Code
D0901 Ammonium salts for the disinfection of medical devices
Device Class
Class IIb
Market of Registration
Belgium

Manufacturer details

EUDAMED SRN
BE-MF-000024078

Other devices from Laboratoire Huckert's International

See all devices from Laboratoire Huckert's International →

Properties & raw data

Show properties, registry sources and raw records
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

Sources (1)

  • EUDAMED d422b2c7-11a9-4b54-8293-a86e761f32f6 61 fields · synced 22 Oct 2026