Data from EUDAMED, last updated Aug 21, 2026
570748030101071007F3 references
570748030101071007FNo device characteristics flagged
Basic 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.
R01030201Endotracheal tubes, cuffed, not reinforced3 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 |
|---|---|---|---|---|---|
| VivaSight™ 2 SLT Kit - 7.0 mm | VivaSight™ 2 SLT Kit - 7.0 mm | 412701000 | 05707480145829 | 1 | On the market |
| VivaSight™ 2 SLT Kit - 7.5 mm | VivaSight™ 2 SLT Kit - 7.5 mm | 412751000 | 05707480145881 | 1 | On the market |
| VivaSight™ 2 SLT Kit - 8.0 mm | VivaSight™ 2 SLT Kit - 8.0 mm | 412801000 | 05707480145935 | 1 | On the market |