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GynoLab (20 tests/box)

by Dyonmed SA Greece EUDAMED

Ref DMAMFL322-20 EMDN W0101060499

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-05200251202436 Basic UDI-DIDate14 Nov 2023RegisteredStatusActive

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDD Expiring

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
GynoLab
Model / Reference
DMAMFL322-20
Primary DI / UDI-DI
05200251202436
Basic UDI-DI
B-05200251202436
EMDN Code
W0101060499 Multiple parameters poc - other
Device Class
Class IVD General
Market of Registration
Greece

Manufacturer details

EUDAMED SRN
GR-MF-000033588

Other devices from Dyonmed SA

See all devices from Dyonmed SA →

Properties & raw data

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

Sources (1)

  • EUDAMED 2fa924ac-159d-4c66-975d-24831cc7a222 61 fields · synced 22 Oct 2026