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Placental Growth Factor Detection Kit (Fluorescence Dry Quantitative Immunoassay)

by Joinstar Biomedical Technology Co., Ltd. EUDAMED

Active European Union

Ref /Model 25 Test/Kit

Regulatory status

as of 27 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-06921026709514 Basic UDI-DIDate23 Sep 2026RegisteredStatusActive

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  • Withdrawn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

Device Name
Placental Growth Factor Detection Kit (Fluorescence Dry Quantitative Immunoassay)
Model / Reference
25 Test/Kit, /
Primary DI / UDI-DI
06921026709514
Basic UDI-DI
B-06921026709514
EMDN Code
W0102050211 Placental growth factor (pre-eclampsia)
Device Class
Class IVD General
Market of Registration
Greece

Manufacturer details

EUDAMED SRN
CN-MF-000001083
Authorised representative
CMC Medical Devices & Drugs SL ES-AR-000000293

Other devices from Joinstar Biomedical Technology Co., Ltd.

Properties

  • 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