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Progesterone ELISA

by Dia.Metra Srl Italy EUDAMED

Ref DKO006

EMDN W0102050106

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number8034049110064UH Basic UDI-DIDate24 Oct 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/IVDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Progesterone ELISA
Model / Reference
DKO006
Primary DI / UDI-DI
08034049110064
Basic UDI-DI
8034049110064UH
Direct Marketing DI
08034049110064
EMDN Code
W0102050106 Progesterone
Device Class
Class B
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000027206

Other devices from Dia.Metra Srl

See all devices from Dia.Metra Srl →

Properties & raw data

Show properties, registry sources and raw records
  • Professional Testing
Other properties (10)
  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No

Sources (1)

  • EUDAMED 41f46fcf-2b5e-44ef-af2a-459f16fa10f6 61 fields · synced 24 Oct 2026