- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 31, 2026
805630062FTPR107DX4 references
805630062FTPR107DXNo device characteristics flagged
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 →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.
V9017Oral administration preparations not included in other classes4 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 |
|---|---|---|---|---|---|
| Quixx Dor de garganta 100 mL PT | Quixx Dor de garganta 100 mL PT | FTPR107 | 08056300622161 | 1 | On the market |
| Quixx Sore Throat 100 ml EE, LT | Quixx Sore Throat 100 ml EE, LT | FTPR107 | 08056300620938 | 1 | On the market |
| Quixx Sore Throat 100 mL EE, LV, LT | Quixx Sore Throat 100 mL EE, LV, LT | FTPR107 | 08056300622154 | 1 | On the market |
| Quixx Sore Throat 100 mL FI, SE | Quixx Sore Throat 100 mL FI, SE | FTPR107 | 08056300620945 | 1 | On the market |