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MONO-VIDITEST anti-Pseudomonas aeruginosa IgG

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

Ref K-430-12Model MONO-VIDITEST anti-Pseudomonas aeruginosa IgG

EMDN W0105010901

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDD NumberB-18594036044309 Basic UDI-DIDate22 Jun 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

Model / Reference
MONO-VIDITEST anti-Pseudomonas aeruginosa IgG, K-430-12
Primary DI / UDI-DI
18594036044309
Basic UDI-DI
B-18594036044309
EMDN Code
W0105010901 Pseudomonas aeruginosa antibody igg
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 d6d15702-0cd1-4ff4-8c89-72219a113658 61 fields · synced 24 Oct 2026