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ABX Minotrol Retic

by Horiba Abx SAS France EUDAMED

Ref 2072202Model 2072201, 2072202, 1300136023, 1300136026, 1300136029

EMDN W0103010506

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number361023minotrol_reticB2 Basic UDI-DIDate5 Jun 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/IVDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Model / Reference
2072201, 2072202, 1300136023, 1300136026, 1300136029
Primary DI / UDI-DI
03610230008904
Basic UDI-DI
361023minotrol_reticB2
EMDN Code
W0103010506 Reticulocyte controls
Device Class
Class B
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000000320

Other devices from Horiba Abx SAS

See all devices from Horiba Abx SAS →

Properties & raw data

Show properties, registry sources and raw records
  • Human Tissues
  • Animal Tissues
  • Reagent
  • Professional Testing
Other properties (7)
  • Sterile: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No

Sources (1)

  • EUDAMED d054cdbe-d9cc-4086-807f-5ca5782bfec4 61 fields · synced 22 Oct 2026