- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 30, 2026
361580LIFTY56B6 references
361580LIFTY56BNo 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.
V0805030102Electric mobile lifts6 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 |
|---|---|---|---|---|---|
| LIFTY 5 - GRIS 7001/7031 - SANS SANGLE | LIFTY 5 - GRIS 7001/7031 - SANS SANGLE | 5010054S1 | 03615800004935 | 1 | On the market |
| LIFTY 5 D - GRIS 7001/7031 - SANS SANGLE | LIFTY 5 D - GRIS 7001/7031 - SANS SANGLE | 5010054S6 | 03615800042104 | 1 | On the market |
| LIFTY 5 D40+ - GRIS 7001/7031 - SANS SANGLE | LIFTY 5 D40+ - GRIS 7001/7031 - SANS SANGLE | 5010140S01 | 03615800048786 | 1 | On the market |
| LIFTY 5 D50 - GRIS 7001/7031 - SANS SANGLE | LIFTY 5 D50 - GRIS 7001/7031 - SANS SANGLE | 5010141S01 | 03615800048793 | 1 | On the market |
| LIFTY 5 DL - GRIS 7001/7031 - SANS SANGLE | LIFTY 5 DL - GRIS 7001/7031 - SANS SANGLE | 5010055S01 | 03615800048557 | 1 | On the market |
| LIFTY 5 UK STD - GRIS 7001/7031 - SANS SANGLE | LIFTY 5 UK STD - GRIS 7001/7031 - SANS SANGLE | 5010054S2 | 03615800038534 | 1 | On the market |