- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jun 19, 2026
697683823P200700EQ4 references
697683823P200700EQ6211186CE016211186TD01Basic 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.
W0105090601Coronavirus / influenza - rt & poc4 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 |
|---|---|---|---|---|---|
| COVID-19/Flu A+B Ag Rapid Test | COVID-19/Flu A+B Ag Rapid Test | P2007C01 | 16976838230531 | 1 | On the market |
| COVID-19/Flu A+B Ag Rapid Test | COVID-19/Flu A+B Ag Rapid Test | P2007C20 | 16976838230562 | 20 | On the market |
| COVID-19/Flu A+B Ag Rapid Test | COVID-19/Flu A+B Ag Rapid Test | P2007C05 | 16976838230555 | 5 | On the market |
| COVID-19/Flu A+B Ag Rapid Test | COVID-19/Flu A+B Ag Rapid Test | P2007C02 | 16976838230548 | 2 | On the market |