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EUDAMED last updated this device on May 25, 2026
6936895BS0092J069368953003596936895BS0092JBS009(01)06936895300359
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.
W0202010101AUTOMATED WHOLE BLOOD HEMATOLOGY ANALYSERS - LOW ROUTINE (Throughput <= 100 samples/hr)No certificate specifically references this device's Basic UDI-DI.
Primary placement in Germany; available across 1 country total.
Placed on the market in Germany; per-country availability dates not published.
CN-MF-000025015No 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.B-06971674868286On the market5′-Nucleotidase (5’-NT) Test Kit (Colorimetric)B-06971674866251On the market5′-Nucleotidase (5’-NT) Test Kit (Colorimetric)B-06971674866244On the market5′-Nucleotidase (5’-NT) Test Kit (Colorimetric)B-06971674866206On the market5′-Nucleotidase (5’-NT) Test Kit (Colorimetric)B-06971674866220On the market