- Role
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- Date of registration
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EUDAMED last updated this device on Mar 27, 2026
7350012440237RYSE-MF-0000169034 warnings recorded — scroll inside the panel to see all entries.
CW012CW027CW010CW015Primary placement in XI; available across 14 countries total.
| Country | On market since | Until |
|---|---|---|
| XIPrimary placement | Apr 1, 2025 | Still on market |
| Austria | Apr 1, 2025 | Still on market |
| Belgium | Apr 1, 2025 | Still on market |
| Germany | Apr 1, 2025 | Still on market |
| Denmark | Apr 1, 2025 | Still on market |
| Spain | Apr 1, 2025 | Still on market |
| Finland | Apr 1, 2025 | Still on market |
| France | Apr 1, 2025 | Still on market |
| Italy | Apr 1, 2025 | Still on market |
| Luxembourg | Apr 1, 2025 | Still on market |
| Netherlands | Apr 1, 2025 | Still on market |
| Norway | Apr 1, 2025 | Still on market |
| Poland | Apr 1, 2025 | Still on market |
| Sweden | Apr 1, 2025 | Still on market |
(01)07350012440237
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.