Skip to content

attomol® Haemochromatosis Duplex Realtime LT

by Attomol GmbH Molekulare Diagnostika Germany EUDAMED

Ref REF1182Model attomol® Haemochromatosis Duplex Realtime LT EMDN W0106010105

Regulatory status

as of 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number42504148HFEDuplexLTUV Basic UDI-DIDate21 Jul 2026RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 25 Oct 2026

Device Name
attomol® Haemochromatosis Duplex Realtime LT (20)
Model / Reference
attomol® Haemochromatosis Duplex Realtime LT, REF1182
Primary DI / UDI-DI
04250414811822
Basic UDI-DI
42504148HFEDuplexLTUV
EMDN Code
W0106010105 Haemochromatosis
Device Class
Class C
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000026028

Other devices from Attomol GmbH Molekulare Diagnostika

See all devices from Attomol GmbH Molekulare Diagnostika →

Properties & raw data

Show properties, registry sources and raw records
  • Reagent
  • Professional Testing
Other properties (9)
  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No

Sources (1)

  • EUDAMED 04250414811822|42504148HFEDUPLEXLTUV 61 fields · synced 25 Oct 2026