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- Date of registration
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EUDAMED last updated this device on May 26, 2026
69268026GeneXE600000001P20692680260562269268026GeneXE600000001P2GeneX E6(01)06926802605622
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.
W02050106DNA GENOMIC PREPARATION DEVICES1 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 Chemiluminescence Immunoassay Analyzer69268026ImmuF60001KSOn the marketFully Automated Blood Grouping System69268026BT30000000000018JOn the marketFully Automated Blood Grouping System69268026BT30000000000018JOn the marketFully-automated Haemostasis Analyzer69268026HameaTX001V7On the market