- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 24, 2026
76300391ESWT006-TG3 references
76300391ESWT006-TGBasic 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.
Z12040203Dermal regeneration equipmentZ120622Muscle stimulatorsZ12101106Neurological stimulatorsZ12139001Shock wave therapy equipmentZ12169002Urological stimulatorsZ12169004Erectile dysfunction stimulators3 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 |
|---|---|---|---|---|---|
| CELLIMPACT | CELLIMPACT | 27100.0100 | 07630039101695 | 1 | On the market |
| DUOLITH SD1 T-TOP | DUOLITH SD1 T-TOP | 21362.1000 | 07630039101626 | 1 | On the market |
| DUOLITH® SD1 T-TOP | DUOLITH® SD1 T-TOP | 21362.1001 | 07630039101916 | 1 | On the market |