- Role
- Country
- Date of registration
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EUDAMED last updated this device on May 29, 2026
53915118586413EIE-MF-000002373No 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.Primary placement in Ireland; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| IrelandPrimary placement | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0104080599MANUAL SUSCEPTIBILITY TESTING - OTHER