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ReLIA

by ReLIA Biotechnologies (Jiangsu), Inc. China EUDAMED

Ref RF16395-50T

EMDN W0102039002

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR NumberB-06971354101962 Basic UDI-DIDate22 May 2026RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/IVDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 22 Oct 2026

Device Name
Beta2 - Microglobulin Test (Fluorescence Immunoassay)
Model / Reference
RF16395-50T
Primary DI / UDI-DI
06971354101962
Basic UDI-DI
B-06971354101962
EMDN Code
W0102039002 Beta2-microglobulin
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.

  • ReLIA

    IVD General
  • ReLIA

    IVD General
  • ReLIA

    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 1af38a51-034c-493d-b9fa-b72da8c5aa48 61 fields · synced 22 Oct 2026