- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 29, 2026
37004822IMPDIVA00003UZFR-MF-000007304No certificates registered for this manufacturer.
No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.Primary placement in France; available across 15 countries total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Nov 19, 2024 | Still on market |
| Austria | Still on market | |
| Belgium | Still on market | |
| Czechia | Still on market | |
| Germany | Still on market | |
| EL | Still on market | |
| Spain | Still on market | |
| Croatia | Still on market | |
| Hungary | Still on market | |
| Italy | Still on market | |
| Latvia | Still on market | |
| Poland | Still on market | |
| Portugal | Still on market | |
| Slovenia | Still on market | |
| Slovakia | Still on market |
(01)03700482299097
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
P09070199SPINAL FUSION SYSTEMS - OTHER