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EUDAMED last updated this device on Jun 14, 2023
B-08719327116128NL-MF-0000027041 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 | Apr 28, 2017 | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0105040311HSV - NA REAGENTSW0104080207MYCOPLASMA / UREAPLASMA - (INCL. COMBINED ID-AST)W0105010305SYPHILIS DETECTION BY NA REAGENTSW0105070501STIS / STDS (C.TRACHOMATIS, N.GONORRHOEAE ,M.GENITALIUM, T.VAGINALIS, UREAPLASMA SPP….) COMBINATION - MULTIPLEX NA REAGENTSW0105010803MYCOPLASMA DETECTION BY NA REAGENTSW0105010117CHLAMYDIA TRACHOMATIS DETECTION BY NA REAGENTS87193271161PFCC-2SKVOn the marketGastroFinder® 2SMART87193271161PF5600-2SVQOn the marketMeningoFinder® 2SMARTB-08719327116111On the marketRealAccurate® Quadruplex Atypical Bacteria PCR kitB-08719327497944On the marketRealAccurate® Quadruplex Color Compensation v587193274979PFCC-Rv5QROn the marketNo 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.