- Role
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EUDAMED last updated this device on Mar 10, 2026
7350012440121RCSE-MF-0000169035 warnings recorded — scroll inside the panel to see all entries.
CW015CW027CW010CW009CW007Primary placement in Sweden; available across 16 countries total.
| Country | On market since | Until |
|---|---|---|
| SwedenPrimary placement | Mar 25, 2022 | Still on market |
| Austria | Mar 24, 2022 | Still on market |
| Belgium | Mar 25, 2022 | Still on market |
| Germany | Mar 25, 2022 | Still on market |
| Denmark | Mar 25, 2022 | Still on market |
| Spain | Mar 25, 2022 | Still on market |
| Finland | Mar 25, 2022 | Still on market |
| France | Mar 25, 2022 | Still on market |
| Ireland | Mar 25, 2022 | Still on market |
| Italy | Mar 25, 2022 | Still on market |
| Netherlands | Mar 24, 2022 | Still on market |
| Norway | Mar 25, 2022 | Still on market |
| Poland | Mar 24, 2022 | Still on market |
| Portugal | Mar 25, 2022 | Still on market |
| Türkiye | Still on market | |
| XI | Mar 25, 2022 | Still on market |
(01)07350012440121
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.
Z12062899NEUROMUSCULAR STIMULATION EQUIPMENT - OTHERNo 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.