- Role
- Country
- Date of registration
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EUDAMED last updated this device on Mar 27, 2026
7350012440015RCSE-MF-0000169034 warnings recorded — scroll inside the panel to see all entries.
CW012CW027CW010CW015Primary placement in Sweden; available across 18 countries total.
| Country | On market since | Until |
|---|---|---|
| SwedenPrimary placement | Jun 1, 2019 | Still on market |
| Austria | May 31, 2021 | Still on market |
| Belgium | Feb 15, 2020 | Still on market |
| Germany | Jun 1, 2020 | Still on market |
| Denmark | Jan 15, 2020 | Still on market |
| EL | Jun 12, 2024 | Still on market |
| Spain | Jun 1, 2019 | Still on market |
| Finland | Jan 10, 2020 | Still on market |
| France | Jun 1, 2021 | Still on market |
| Ireland | May 1, 2021 | Still on market |
| Italy | Jun 1, 2019 | Still on market |
| Luxembourg | Jun 12, 2024 | Still on market |
| Netherlands | Jan 15, 2020 | Still on market |
| Norway | Jan 15, 2020 | Still on market |
| Poland | May 31, 2020 | Still on market |
| Portugal | Feb 1, 2020 | Still on market |
| Türkiye | Jun 12, 2024 | Still on market |
| XI | Jun 1, 2019 | Still on market |
(01)07350012440015
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.