- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jun 11, 2026
B-CNMF000054349DP024GE1 reference
B-CNMF000054349DP024GEBasic 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.
W0102160599Drugs of abuse/toxicology rt & poc - other1 reference
| Trade name | Reference / catalog number | UDI-DI code | Quantity | Status |
|---|---|---|---|---|
| TRA Rapid Test Kit (Colloidal gold method) | DP024 | D-CNMF000054349DP024GE | 1 | On the market |