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Ampliquality Hcv Type Plus

by AB ANALITICA srl 3 variants

Ref 03-05-20 MModel AMPLIQUALITY HCV TYPE PLUS

Active European Union

CE IVDR

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR Number803362278AINFrk00000000T5 Basic UDI-DI 08033622786269UDI-DIDate1 Sep 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  • Withdrawn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/IVDR Active

Specification

EUDAMED

Model / Reference
AMPLIQUALITY HCV TYPE PLUS, 03-05-20 M
Primary DI / UDI-DI
08033622786269
Basic UDI-DI
803362278AINFrk00000000T5
Direct Marketing DI
08033622786269
EMDN Code
W0105020309 Hepatitis c virus (hcv) genotyping - na reagents
Device Class
Class C
EU market of registration
Italy

Manufacturer details

EUDAMED SRN
IT-MF-000032625

Other devices from AB ANALITICA srl

See all devices from AB ANALITICA srl →

Properties

  • Animal Tissues
  • Microbial Substances
  • Reagent
  • Professional Testing

Other properties (7)

  • Sterile: No
  • Human Tissues: No
  • Self Testing: No
  • Near-Patient Testing: No
  • Companion Diagnostics: No
  • Surgical Instrument: No
  • New Device: No