- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 31, 2026
42516207007K34 references
42516207007K3Basic 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.
W05019099Samples collection devices - other4 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 |
|---|---|---|---|---|---|
| cerascreen® Fructose Intolerance Test | cerascreen® Fructose Intolerance Test | 99010517 | 04251620707237 | 1 | On the market |
| cerascreen® Fructoseunverträglichkeits-Test | cerascreen® Fructoseunverträglichkeits-Test | 99010148 | 04251620708623 | 1 | On the market |
| cerascreen® Fructoseunverträglichkeits-Test | cerascreen® Fructoseunverträglichkeits-Test | 99010034 | 04251620708616 | 1 | On the market |
| cerascreen® Laktoseintoleranz Test | cerascreen® Laktoseintoleranz Test | 99010033 | 04251620700306 | 1 | On the market |