- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on Jul 12, 2023
B-08720791370961NL-MF-000000064No 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.7 warnings recorded — scroll inside the panel to see all entries.
CW011CW009CW007CW032CW001CW010CW027Primary placement in Netherlands; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | Jul 11, 2023 | Still on market |
(01)08720791370961
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z12101185PERIPHERAL OR CENTRAL NEURO STIMULATION AND ASSESSMENT INSTRUMENTS - CONSUMABLES