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Irma Acth

by IMMUNOTECH s.r.o. Czech Republic EUDAMED

Ref IM2030Model IM2030, B89463

EMDN W0102060401

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number150995905ACTHIRMAYL Basic UDI-DIDate1 Oct 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
IM2030, B89463
Primary DI / UDI-DI
15099590216429
Basic UDI-DI
150995905ACTHIRMAYL
EMDN Code
W0102060401 Adrenocorticotropic hormone
Device Class
Class C
Market of Registration
Czechia

Manufacturer details

EUDAMED SRN
CZ-MF-000001761

Other devices from IMMUNOTECH s.r.o.

See all devices from IMMUNOTECH s.r.o. →

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 d42bd04e-81bf-4194-a0cb-0e09a4a049b5 61 fields · synced 22 Oct 2026