- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 22, 2026
5207003MTSOFLEXMEDASR6 references
5207003MTSOFLEXMEDASRNo 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.
V08068002Bed supports6 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 |
|---|---|---|---|---|---|
| SOFLEX MED D 25/10 | SOFLEX MED D 25/10 | SOFLEX MED D 25/10 | 52070030108062 | 1 | On the market |
| SOFLEX MED D 25/12 | SOFLEX MED D 25/12 | SOFLEX MED D 25/12 | 52070030108130 | 1 | On the market |
| SOFLEX MED D 25/15 | SOFLEX MED D 25/15 | SOFLEX MED D 25/15 | 52070030108208 | 1 | On the market |
| SOFLEX MED D 30/10 | SOFLEX MED D 30/10 | SOFLEX MED D 30/10 | 52070030108376 | 1 | On the market |
| SOFLEX MED D 30/12 | SOFLEX MED D 30/12 | SOFLEX MED D 30/12 | 52070030108444 | 1 | On the market |
| SOFLEX MED D 30/15 | SOFLEX MED D 30/15 | SOFLEX MED D 30/15 | 52070030108512 | 1 | On the market |