- Role
- Country
- Date of registration
- Address
EUDAMED last updated this device on May 26, 2026
69268026ImmuF60001KS0692680260273769268026ImmuF60001KSImmu F6(01)06926802602737
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.
W0201020101AUTOMATED IMMUNOCHEMISTRY ANALYSERS - LOW ROUTINE (Throughput <= 100 test/h)1 warning recorded — scroll inside the panel to see all entries.
CW010No certificate specifically references this device's Basic UDI-DI.
Primary placement in Netherlands; available across 1 country total.
Placed on the market in Netherlands; per-country availability dates not published.
CN-MF-000005925No 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.69268026ImmuF60001KSOn the marketAutoMated Nucleic Acid Extraction System69268026GeneXE600000001P2On the marketAutoMated Nucleic Acid Extraction System69268026GeneXE600000001P2On the marketFully Automated Blood Grouping System69268026BT30000000000018JOn the marketFully Automated Blood Grouping System69268026BT30000000000018JOn the market