- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Apr 27, 2026
735013281SAM/MRI-019ZRSE-MF-000053189No 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 Sweden; available across 14 countries total.
| Country | On market since | Until |
|---|---|---|
| SwedenPrimary placement | Jan 1, 2026 | Still on market |
| Austria | Jan 1, 2026 | Still on market |
| Belgium | Jan 1, 2026 | Still on market |
| Germany | Jan 1, 2026 | Still on market |
| Denmark | Jan 1, 2026 | Still on market |
| Spain | Jan 1, 2026 | Still on market |
| Finland | Jan 1, 2026 | Still on market |
| France | Jan 1, 2026 | Still on market |
| Iceland | Jan 1, 2026 | Still on market |
| Italy | Jan 1, 2026 | Still on market |
| Lithuania | Jan 1, 2026 | Still on market |
| Netherlands | Jan 1, 2026 | Still on market |
| Norway | Jan 1, 2026 | Still on market |
| Poland | Jan 1, 2026 | Still on market |
(01)07350132811771
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.
C01020499SUBCUTANEOUS IMPLANTABLE VENOUS ACCESS PORT SYSTEMS - OTHER