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EUDAMED last updated this device on May 20, 2026
697530920G521E4Flow Cytometer is an EU IVDR-regulated in vitro diagnostic registered in EUDAMED. It is classified as IVDR Class A. Manufactured by Beijing Challen Biotechnology Co., Ltd.. Placed on the EU market in Czechia. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
06975309200663697530920G521E4C.LS.A2000T2(01)06975309200663
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.
W0202040103CYTOFLOWMETERS - HIGH ROUTINE1 warning recorded — scroll inside the panel to see all entries.
CW999No certificate specifically references this device's Basic UDI-DI.
Primary placement in Czechia; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| CzechiaPrimary placement | Still on market |
CN-MF-000023656No 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.