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EUDAMED last updated this device on Feb 4, 2026
805768091CNexViralLV_015JCloNext Viral Nucleic Acid Extraction Kit LV is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Clonit srl. Placed on the EU market in Italy. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
08057680911098OP02016-48(01)08057680911098
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0105900101REAGENTS FOR DNA AND/OR RNA EXTRACTION AND PREPARATION: BACTERIA AND/OR VIRUSIT-MF-000022196The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Primary placement in Italy; available across 1 country total.
Placed on the market in Italy; per-country availability dates not published.
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.
View in glossary →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.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
View in glossary →UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
View in glossary →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.
View in glossary →Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
View in glossary →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.No certificate specifically references this device's Basic UDI-DI.
805768091CNextTissue_016EOn the marketCLONEXT TOTAL RNA EXTRACTION KIT805768091CNextTotRNA_01CKOn the marketCloNext Viral Nucleic Acid Extraction Kit805768091CNexViralNA_01ZJOn the marketCloNext Viral RNA Extraction Kit805768091CNextViral_01LUOn the marketCLONEXT VIRAL/PATHOGEN NUCLEIC ACID EX KIT A805768091CNextViralA_01N2On the marketCLONEXT VIRAL/PATHOGEN NUCLEIC ACID EX KIT B805768091CNextViralB_01N9On the market