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ELISA-VIDITEST Interferon γ

by VIDIA spol. s r.o. Czech Republic EUDAMED

Ref ODZ-326Model ELISA-VIDITEST Interferon γ EMDN W01030601

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-28594036043262 Basic UDI-DIDate29 Jun 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  • Withdrawn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 · synced 23 Oct 2026

Model / Reference
ELISA-VIDITEST Interferon γ, ODZ-326
Primary DI / UDI-DI
28594036043262
Basic UDI-DI
B-28594036043262
EMDN Code
W01030601 INTERFERONS (α, β, ɣ…)
Device Class
Class IVD General
Market of Registration
Czechia

Manufacturer details

EUDAMED SRN
CZ-MF-000036964

Other devices from VIDIA spol. s r.o.

See all devices from VIDIA spol. s r.o. →

Properties & raw data

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

Sources (1)

  • EUDAMED 2813a3c3-1cba-4481-bc73-12aaba4337e1 61 fields · synced 23 Oct 2026