- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 30, 2026
3661379FAB020002AEF4 references
3661379FAB020002AEFBasic 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.
A0399Tubular 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 |
|---|---|---|---|---|---|
| DOUBLEFLO Day Tube Set | DOUBLEFLO Day Tube Set | 72205772 | 03661379223055 | 1 | On the market |
| DOUBLEFLO OUTFLOW TUBE SET | DOUBLEFLO OUTFLOW TUBE SET | 72205765 | 03661379223086 | 1 | On the market |
| DOUBLEFLO PATIENT TUBE SET | DOUBLEFLO PATIENT TUBE SET | 72205773 | 03661379223062 | 1 | On the market |
| DOUBLEFLO Inflow Tube Set | DOUBLEFLO Inflow Tube Set | 72205774 | 03661379223079 | 1 | On the market |