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- Date of registration
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EUDAMED last updated this device on Nov 8, 2023
++B941KQSOFT6F20203 is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by KineQuantum. Placed on the EU market in France. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
B941202030++B941KQSOFT6F20203B941202030
DataMatrix generation currently supports GS1-issued UDIs. HIBCC / ICCBBA support is coming.
European Medical Device Nomenclature — the EU product classification assigned to this device.
Z12069099VARIOUS PHYSIOTHERAPY AND REHABILITATION INSTRUMENTS - OTHER1 warning recorded — scroll inside the panel to see all entries.
CW010No certificate specifically references this device's Basic UDI-DI.
Primary placement in France; available across 3 countries total.
| Country | On market since | Until |
|---|---|---|
| FrancePrimary placement | Nov 8, 2023 | May 31, 2024 |
| Belgium | Nov 8, 2023 | May 31, 2024 |
| Luxembourg | Nov 8, 2023 | May 31, 2024 |
FR-MF-000024566No 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.