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ELISA-VIDITEST anti-TBEV IgG and IgG avidity

by VIDIA spol. s r.o. 2 variants

Ref OD-170Model ELISA-VIDITEST anti-TBEV IgG and IgG avidity

Active European Union

CE IVDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None, self-declared

Class I: no certifier involved

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-08594036041707 Basic UDI-DI 08594036041707UDI-DIDate23 Jun 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/IVDD Active

Specification

EUDAMED

Model / Reference
ELISA-VIDITEST anti-TBEV IgG and IgG avidity, OD-170
Primary DI / UDI-DI
08594036041707
Basic UDI-DI
B-08594036041707
EMDN Code
W0105040612 Fsme virus
Device Class
Class IVD General
EU market of registration
Czechia

Manufacturer details

EUDAMED SRN
CZ-MF-000036964

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Properties

  • 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