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Ds-Eia-Steroid-Progesterone

by RPC Diagnostic Systems Ltd. Russia EUDAMED

Ref RH-351/1.1 EMDN W0102050106

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-04605979401900 Basic UDI-DIDate9 Oct 2025RegisteredStatusWithdrawn No longer placed on the EU market

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDD Withdrawn

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
“ds-Eia-Steroid-Progesterone” Enzyme Immunoassay for the Quantitative Determination of Progesterone Concentration
Model / Reference
RH-351/1.1
Primary DI / UDI-DI
04605979401900
Basic UDI-DI
B-04605979401900
EMDN Code
W0102050106 Progesterone
Device Class
Class IVD General

Manufacturer details

EUDAMED SRN
RU-MF-000043555
Authorised representative
AB Diagnostic Systems GmbH DE-AR-000025750

Properties & raw data

Show properties, registry sources and raw records
  • Human Tissues
  • Animal Tissues
  • Reagent
  • Professional Testing
Other properties (6)
  • Sterile: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No

Sources (1)

  • EUDAMED 6336206a-8cb7-4e27-b7b7-82f02b8816fa 61 fields · synced 24 Oct 2026