- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Aug 18, 2026
697384322FQD003GU2 references
697384322FQD003GUBasic 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 →SRN
An SRN is the unique EUDAMED identifier assigned to a manufacturer, authorised representative or importer when it registers as an actor.
View in glossary →SRN
An SRN is the unique EUDAMED identifier assigned to a manufacturer, authorised representative or importer when it registers as an actor.
View in glossary →European Medical Device Nomenclature — the EU product classifications carried across this device family's references.
W02050116Nucleic acid testing integrated extraction /amplification /detection systems2 references
| Product | Trade name | Reference / catalog number | 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 → | Quantity | Status |
|---|---|---|---|---|---|
| LineGene K Plus Fluorescent Quantitative Detection System | LineGene K Plus Fluorescent Quantitative Detection System | FQD-48A(EA2) | 06973843221243 | 1 | On the market |
| LineGene K Plus Fluorescent Quantitative Detection System | LineGene K Plus Fluorescent Quantitative Detection System | FQD-48A(EA4) | 06973843221250 | 1 | On the market |