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- Date of registration
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IT-MF-000029422LIAISON® QuantiFERON® Software is an IVDD-legacy in vitro diagnostic registered in EUDAMED. It is classified as IVDD — General. Manufactured by DiaSorin Italia S.p.A.. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
EUDAMED last updated this device on Jun 24, 2026
B-08056771103473Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)08056771103473
1 warning recorded — scroll inside the panel to see all entries.
Viz návod k použití v elektronické podobě (CS); Se den elektroniske brugsanvisning (DA); Elektronische Gebrauchs-anweisung beachten (DE); Raadpleeg de Elektronische gebruiks-aanwijzing (NL); Συμβουλευτείτε τις ηλεκτρονικές οδηγίες χρήσης (EL); Consulte las instrucciones electrónicas de uso (ES); Käänny elektronisen käyttöohjeen puoleen (FI); Lire la notice d’utilisation électronique (FR); Olvassa el az elektronikus használati utasítást (HU); Leggere le istruzioni per l’uso in formato elettronico (IT); Les den elektroniske bruksanvisningen (NO); Przeczytać elektroniczną instrukcję użycia (PL); Consulte as instruções de utilização electrónicas (PT); Consultaţi instrucţiunile de utilizare electronice (RO); Riaďte sa elektronickými pokynmi na použitie (SK); Läs igenom den elektroniska bruksanvisningen (SV);(Consult electronic instructions for use (EN); Kullanmadan önce elektronik ortamdaki açıklamalara bakınız (TR);
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
Primary placement in Italy; available across 32 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | — | Still on market |
| Austria | — | Still on market |
| Belgium | — | Still on market |
| Bulgaria | — | Still on market |
| Cyprus | — | Still on market |
| Czechia | — | Still on market |
| Germany | — | Still on market |
| Denmark | — | Still on market |
| Estonia | — | Still on market |
| EL | — | Still on market |
| Spain | — | Still on market |
| Finland | — | Still on market |
| France | — | Still on market |
| Croatia | — | Still on market |
| Hungary | — | Still on market |
| Ireland | — | Still on market |
| Iceland | — | Still on market |
| Liechtenstein | — | Still on market |
| Lithuania | — | Still on market |
| Luxembourg | — | Still on market |
| Latvia | — | Still on market |
| Malta | — | Still on market |
| Netherlands | — | Still on market |
| Norway | — | Still on market |
| Poland | — | Still on market |
| Portugal | — | Still on market |
| Romania | — | Still on market |
| Sweden | — | Still on market |
| Slovenia | — | Still on market |
| Slovakia | — | Still on market |
| Türkiye | — | Still on market |
| XI | — | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
08056771103473Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
B-08056771103473Q0001UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
IVDR risk classes
IVDR risk classes rank in-vitro diagnostic devices from lowest risk (Class A) to highest (Class D), based on the patient and public-health risk of a wrong result.
European Medical Device Nomenclature — the EU product classification assigned to this device.
W02079082VARIOUS GENERAL PURPOSE IVD INSTRUMENTS - SOFTWARE ACCESSORIESB-08056771200127On the marketLIAISON® PSAB-08056771200455On the marketLIAISON® PSA II Gen80567713113203SOn the marketLIAISON® QuantiFERON®-TB Gold PlusB-08056771103282On the marketLIAISON® QuantiFERON®-TB Gold Plus80567713110503LOn the marketLIAISON® QuantiFERON®-TB Gold Plus II80567713110903YOn the marketNo certificate specifically references this device's Basic UDI-DI.
No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.