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MONO-VIDITEST anti-Toxoplasma gondii IgG avidity

by VIDIA spol. s r.o.

Ref KZ-213-12Model MONO-VIDITEST anti-Toxoplasma gondii 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 linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-38594036042132 Basic UDI-DI 38594036042132UDI-DIDate1 Jul 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/IVDD Active

Specification

EUDAMED

Model / Reference
MONO-VIDITEST anti-Toxoplasma gondii IgG avidity, KZ-213-12
Primary DI / UDI-DI
38594036042132
Basic UDI-DI
B-38594036042132
EMDN Code
W0105050104 Toxoplasma antibody igg - avidity
Device Class
Class IVD Annex II List B
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