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EUDAMED last updated this device on May 11, 2026
B-0697167486622006971674866220B-06971674866220R1:20mL×1 R2:10mL×1(702)(01)06971674866220
European Medical Device Nomenclature — the EU product classification assigned to this device.
W010101015'-NUCLEOTIDASENo certificate specifically references this device's Basic UDI-DI.
Primary placement in Germany; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| GermanyPrimary placement | Still on market |
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-06971674866190On the market