Data from EUDAMED, last updated Jul 31, 2026
8050714610000SPMCW9 references
8050714610000SPMCWNo 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 mattresses9 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 |
|---|---|---|---|---|---|
| BIOFIR CALIBER RELAX | BIOFIR CALIBER RELAX | SPM001 401 | 08050714610165 | 1 | On the market |
| BIOFIR HOME CALIBER | BIOFIR HOME CALIBER | SPM002 450 | 08050714610189 | 1 | On the market |
| BIOFIR KUBRIK | BIOFIR KUBRIK | SPM003 490 | 08050714610202 | 1 | On the market |
| CALIBER RELAX | CALIBER RELAX | SPM001 425 | 08050714610172 | 1 | On the market |
| HOME CALIBER | HOME CALIBER | SPM002 485 | 08050714610196 | 1 | On the market |
| HOME CALIBER CON COPRIMATERASSO LANA ANTIDECUBITO BIOFIR | HOME CALIBER CON COPRIMATERASSO LANA ANTIDECUBITO BIOFIR | SPM002 30100 | 08050714610264 | 1 | On the market |
| HOME CALIBER CON MAT MEMOELAST ANTIDECUBITO | HOME CALIBER CON MAT MEMOELAST ANTIDECUBITO | SPM002 80100 | 08050714610318 | 1 | On the market |
| HOME CALIBER CON STUOIA BIOFIR | HOME CALIBER CON STUOIA BIOFIR | SPM002 40100 | 08050714610271 | 1 | On the market |
| KUBRIK | KUBRIK | SPM003 495 | 08050714610219 | 1 | On the market |