- Role
- Country
- Date of registration
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EUDAMED last updated this device on May 8, 2025
805901671SONDEPERINEALIZMIT-MF-0000236162 warnings recorded — scroll inside the panel to see all entries.
CW010CW135Primary placement in Italy; available across 18 countries total.
| Country | On market since | Until |
|---|---|---|
| ItalyPrimary placement | Apr 24, 2025 | Still on market |
| Austria | Apr 24, 2025 | Still on market |
| Belgium | Apr 24, 2025 | Still on market |
| Germany | Apr 24, 2025 | Still on market |
| EL | Apr 24, 2025 | Still on market |
| Spain | Apr 24, 2025 | Still on market |
| Finland | Apr 24, 2025 | Still on market |
| France | Apr 24, 2025 | Still on market |
| Ireland | Apr 24, 2025 | Still on market |
| Iceland | Apr 24, 2025 | Still on market |
| Liechtenstein | Apr 24, 2025 | Still on market |
| Luxembourg | Apr 24, 2025 | Still on market |
| Latvia | Apr 24, 2025 | Still on market |
| Malta | Apr 24, 2025 | Still on market |
| Netherlands | Apr 24, 2025 | Still on market |
| Poland | Apr 24, 2025 | Still on market |
| Portugal | Apr 24, 2025 | Still on market |
| XI | Apr 24, 2025 | Still on market |
(01)08059016710412
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.
U070399PELVIC FLOOR REHABILITATION DEVICES - 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.