- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Apr 29, 2025
038283NA00170ED00382830051323038283NA00170EDMRARR23-59(01)00382830051323
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.
N010101ELECTROMYOGRAPHIC ELECTRODES1 warning recorded — scroll inside the panel to see all entries.
CW011No certificate specifically references this device's Basic UDI-DI.
Primary placement in Ireland; available across 13 countries total.
| Country | On market since | Until |
|---|---|---|
| IrelandPrimary placement | Oct 4, 2024 | Still on market |
| Austria | Oct 4, 2024 | Still on market |
| Cyprus | Oct 4, 2024 | Still on market |
| Germany | Oct 4, 2024 | Still on market |
| Estonia | Oct 4, 2024 | Still on market |
| Spain | Oct 4, 2024 | Still on market |
| France | Oct 4, 2024 | Still on market |
| Italy | Oct 4, 2024 | Still on market |
| Luxembourg | Oct 4, 2024 | Still on market |
| Malta | Oct 4, 2024 | Still on market |
| Netherlands | Oct 4, 2024 | Still on market |
| Poland | Oct 4, 2024 | Still on market |
| Sweden | Oct 4, 2024 | Still on market |
IE-MF-000000799No 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.