- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 25, 2026
366353700025B54 references
366353700025B5Basic 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.
W0103020702Control plasma for haemostasis4 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 |
|---|---|---|---|---|---|
| BIOPHEN™ Abnormal Control Plasma | BIOPHEN™ Abnormal Control Plasma | 223301 | 03663537008313 | 1 | On the market |
| EASYPLASMA™ Control Set | EASYPLASMA™ Control Set | 225601 | 03663537082306 | 1 | On the market |
| Revohem™ Control 2 Lite | Revohem™ Control 2 Lite | AQ518931 | 03663537085819 | 1 | On the market |
| Revohem™ Control 2 Pro | Revohem™ Control 2 Pro | AY003713 | 03663537085826 | 1 | On the market |