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ReLIA

by ReLIA Biotechnologies (Jiangsu), Inc. China EUDAMED

Ref RF16373-50T

EMDN W0102050206

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-06971354101832 Basic UDI-DIDate21 May 2026RegisteredStatusActive

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
The β-subunit of Human Chorionic Gonadotropin Test (Fluorescence Immunoassay)
Model / Reference
RF16373-50T
Primary DI / UDI-DI
06971354101832
Basic UDI-DI
B-06971354101832
EMDN Code
W0102050206 B- human chorionic gonadotropin (incl. subunit)
Device Class
Class IVD General
Market of Registration
Slovenia

Manufacturer details

EUDAMED SRN
CN-MF-000042042
Authorised representative
Luxus Lebenswelt GmbH DE-AR-000005110

Other devices from ReLIA Biotechnologies (Jiangsu), Inc.

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    IVD General

  • ReLIA

    IVD General

  • ReLIA

    IVD General

  • ReLIA

    IVD General

See all devices from ReLIA Biotechnologies (Jiangsu), Inc. →

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 1ddd74e6-9f5a-47c3-bb43-134546056900 61 fields · synced 24 Oct 2026