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Aio-Rhd Fetal DNA Kit

by Genotropy France EUDAMED

Ref GNPY #010-008

EMDN W0103030201

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-03770029504052 Basic UDI-DIDate17 Jun 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Expiring (legacy directive)
  • Not covered

European Union — CE/IVDD Expiring (legacy directive)

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 24 Oct 2026

Device Name
Aio-Rhd Fetal DNA Kit (750)
Model / Reference
GNPY #010-008
Primary DI / UDI-DI
03770029504052
Basic UDI-DI
B-03770029504052
EMDN Code
W0103030201 Rhesus d
Device Class
Class IVD Annex II List A
Market of Registration
France

Manufacturer details

EUDAMED SRN
FR-MF-000026152

Other devices from Genotropy

Properties & raw data

Show properties, registry sources and raw records
  • Reagent
  • Professional Testing
Other properties (8)
  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No

Sources (1)

  • EUDAMED 31363934-c17c-430c-93b7-ee4479768070 61 fields · synced 24 Oct 2026