- Organization name
- UDI-DI code
- Reference / catalog number
IT-MF-000029422LIAISON® SARS-CoV-2 Sample Inactivation Buffer is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. 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 Aug 28, 2026
80567713114924QPrimary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
(01)08056771103770
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
2 warnings recorded — scroll inside the panel to see all entries.
Consult electronic instructions for use (EN); Leggere le istruzioni per l’uso in formato elettronico (IT); Elektronische Gebrauchs-anweisung beachten (DE); Lire la notice d’utilisation électronique (FR); Consulte las instrucciones electrónicas de uso (ES); Consulte as instruções de utilização electrónicas (PT); Συμβουλευτείτε τις ηλεκτρονικές οδηγίες χρήσης (EL); Se den elektroniske brugsanvisning (DA); Les den elektroniske bruksanvisningen (NO); Läs igenom den elektroniska bruksanvisningen (SV); Viz návod k použití v elektronické podobě (CS); Olvassa el az elektronikus használati utasítást (HU); Przeczytać elektroniczną instrukcję użycia (PL); Riaďte sa elektronickými pokynmi na použitie (SK); Вижте електронните инструкции за употреба (BG); Consultaţi instrucţiunile de utilizare electronice (RO); Žr. elektroninę naudojimo instrukciją (LT); Izlasiet elektronisko lietošanas instrukciju (LV); Kullanmadan önce elektronik ortamdaki açıklamalara bakınız (TR); Slijedite elektroničke upute za uporabu (HR)
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.
08056771103770Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
80567713114924Q311492UDI 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.
W0105900201BUFFERS (UNASSIGNABLE ), SUPPLEM. REAGENTS, ETCNo 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.