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Vascular Endothelial Growth Factor Rapid Test Kit (Fluorescence Immunochromatographic Assay)

by Hoyotek Biomedical Co., Ltd. China EUDAMED

Ref IF17-01-20Model Please see the IFU.

EMDN W0102030199

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-06974738205171 Basic UDI-DIDate15 Sep 2023RegisteredStatusActive

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
Fluorescence Immunochromatography Analyzer
Model / Reference
Please see the IFU., IF17-01-20
Primary DI / UDI-DI
06974738205171
Basic UDI-DI
B-06974738205171
EMDN Code
W0102030199 Cancer antigens - other
Device Class
Class IVD General
Market of Registration
Spain

Manufacturer details

EUDAMED SRN
CN-MF-000003570
Authorised representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Other devices from Hoyotek Biomedical Co., Ltd.

See all devices from Hoyotek Biomedical Co., Ltd. →

Properties & raw data

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

Sources (1)

  • EUDAMED e47f7df0-0cb5-4321-bcdb-eed0349ff845 61 fields · synced 22 Oct 2026