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EUDAMED last updated this device on May 18, 2026
697462121Metis3FAutomated Blood Grouping Analyzer is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Aikang MedTech Co., Ltd. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06974621212606697462121Metis3FMetis 200 Plus-8(01)06974621212606
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.
W0202030102AUTOMATED BLOOD GROUPING ANALYSERSNo 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-000027272No 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.697462121LumimateZQOn the market06974621212415697462121FYQS7On the marketAutomated Blood Grouping Analyzer697462121Metis3FOn the marketAutomated Blood Grouping Analyzer697462121Metis3FOn the marketAutomated Blood Grouping Analyzer697462121Metis3FOn the market