- Role
- Country
- Date of registration
- Address
Data from EUDAMED, last updated Jul 31, 2026
6429810258TRIMAXR2H1 reference
6429810258TRIMAXR2HNo 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.
V080702Non active anti-decubitus medical mattresses1 reference
| 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 |
|---|---|---|---|---|---|
| Vevia Tripla Max-R Rescue 200*80*17cm; TRIMAX-R RESC80200 | Vevia Tripla Max-R Rescue 200*80*17cm; TRIMAX-R RESC80200 | Vevia Tripla Max-R | 06429810258588 | 1 | On the market |