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EUDAMED last updated this device on May 28, 2026
73955026122111ALQSE-MF-000000885No 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.1 warning recorded — scroll inside the panel to see all entries.
CW009Primary placement in Finland; available across 5 countries total.
| Country | On market since | Until |
|---|---|---|
| FinlandPrimary placement | Still on market | |
| Denmark | Still on market | |
| Iceland | Still on market | |
| Norway | Still on market | |
| Sweden | Still on market |
(01)07395502056291
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.
V0599CLINICAL PROCEDURES KITS NOT INCLUDED IN OTHER CLASSES - OTHER