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EUDAMED last updated this device on Jun 14, 2023
B-08719327116197NL-MF-000002704No 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.1 warning recorded — scroll inside the panel to see all entries.
CW010Primary placement in Netherlands; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| NetherlandsPrimary placement | Dec 9, 2014 | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0105040505RESPIRATORY SYNCYTIAL VIRUS (RSV) - NA REAGENTSW0105040502ENTEROVIRUS - NA REAGENTSW0105040520RHINOVIRUS - NA REAGENTSW0105010503LEGIONELLA DETECTION BY NA REAGENTSW0105010803MYCOPLASMA DETECTION BY NA REAGENTSW0105010118CHLAMYDIA PNEUMONIAE DETECTION BY NA REAGENTSW0105011607BORDETELLA PERTUSSIS / PARAPERTUSSIS - NA REAGENTSW0105040504INFLUENZA & PARA INFLUENZA - NA REAGENTSW0105040517HUMAN METAPNEUMOVIRUS - NA REAGENTSW0105040519CORONAVIRUS - NA REAGENTSInactiveW0105040518BOCAVIRUS - NA REAGENTSW0105040501ADENOVIRUS - NA REAGENTS87193274979PFCC-Rv5QR