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Cytotest

by Cytodiagnostic srl San Marino EUDAMED

Ref 5FHCT51

EMDN W01020299

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number805151388CYTOTESTD6 Basic UDI-DIDate18 Nov 2024RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Not covered

European Union — CE/IVDR Active

Certificates: none listed in EUDAMED

Specification

EUDAMED · synced 23 Oct 2026

Device Name
Cytotest - Cytotoxic Test
Model / Reference
5FHCT51
Primary DI / UDI-DI
08051513880018
Basic UDI-DI
805151388CYTOTESTD6
Unit of Use DI
08051513880001
EMDN Code
W01020299 Allergy tests - other
Device Class
Class A
Market of Registration
Italy

Manufacturer details

EUDAMED SRN
SM-MF-000045033
Authorised representative
Dott. Carmelo Rizzo IT-AR-000040805

Other devices from Cytodiagnostic srl

Properties & raw data

Show properties, registry sources and raw records
  • Professional Testing
Other properties (10)
  • Sterile: No
  • Human Tissues: No
  • Animal Tissues: No
  • Microbial Substances: No
  • Reagent: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No

Sources (1)

  • EUDAMED 6ec683da-feda-489f-a100-931c0e1e736d 61 fields · synced 23 Oct 2026