- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 26, 2026
69509960FDWCR-402a-DR4R2 references
69509960FDWCR-402a-DR4R6188440CE016188440TD09Basic 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.
W0102160601C-reactive protein - rt & poc2 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 |
|---|---|---|---|---|---|
| CRP Quantitative Test Kit (Time-Resolved FIA) | CRP Quantitative Test Kit (Time-Resolved FIA) | FDWCR-402a-DR | 06950996003797 | 25 | On the market |
| CRP Quantitative Test Kit (Time-Resolved FIA) | CRP Quantitative Test Kit (Time-Resolved FIA) | FDWCR-402a-DR10 | 06950996003780 | 9 | On the market |