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Ovulation Test

by Sanavita Pharmaceuticals GmbH Germany EUDAMED

Ref OVULATIONTEST

EMDN W0102050105

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-OVULATIONTEST3K Basic UDI-DIDate28 Apr 2022RegisteredStatusActive

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 22 Oct 2026

Device Name
Ovulation Test
Model / Reference
OVULATIONTEST
Primary DI / UDI-DI
D-OVULATIONTEST3K
Basic UDI-DI
B-OVULATIONTEST3K
EMDN Code
W0102050105 Luteinising hormone
Device Class
Class IVD devices for self-testing
Market of Registration
Spain

Manufacturer details

EUDAMED SRN
DE-MF-000005463

Other devices from Sanavita Pharmaceuticals GmbH

Properties & raw data

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

Sources (1)

  • EUDAMED 794a0cdb-49cc-4b4d-833c-0273890c4a83 61 fields · synced 22 Oct 2026