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EUDAMED last updated this device on Mar 27, 2026
7350012440145RSSE-MF-000016903No 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.2 warnings recorded — scroll inside the panel to see all entries.
CW027CW010Primary placement in XI; available across 9 countries total.
| Country | On market since | Until |
|---|---|---|
| XIPrimary placement | May 31, 2022 | Still on market |
| Austria | May 31, 2022 | Still on market |
| Belgium | May 31, 2022 | Still on market |
| Germany | May 31, 2022 | Still on market |
| Finland | May 31, 2022 | Still on market |
| France | May 31, 2022 | Still on market |
| Ireland | May 31, 2022 | Still on market |
| Italy | May 31, 2022 | Still on market |
| Luxembourg | May 31, 2022 | Still on market |
(01)07350012440145
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 - OTHER