ANVISA registration

cobas® 4800 HPV - Amplification/Detection Kit

Registration 10287410898. PAPILOMAVÍRUS HUMANO (HPV)

Registration details

Registration number10287410898
Application number25351414690201045
Technical namePAPILOMAVÍRUS HUMANO (HPV)
Risk classIII
Published on04/10/2010
ValidityValid until 04/10/2035

Registration holder

Legal nameROCHE DIAGNÓSTICA BRASIL LTDA
CNPJ30.280.358/0001-86

Manufacturer

  • ROCHE MOLECULAR SYSTEMS, INC ESTADOS UNIDOS DA AMÉRICA

Other registrations held by ROCHE DIAGNÓSTICA BRASIL LTDAview all

CARDIAC D DIMERO

10287410066

ROCHE AMONIA/ETANOL/CO2 CALIBRATOR

10287410069

CERU, Ceruloplasmina.

10287410074

COBAS INTEGRA FP-CAL (FP CALIBRATION)

10287410075

Família ROCHE AMONIA/ETANOL/ CO2 CONTROLS

10287410079

CARDIAC D DIMERO CONTROLE

10287410080

Source: ANVISA

Source: ANVISA open data, medical device file, updated daily. The public database provides registration validity, rather than registration status: this registration may have been cancelled before its expiry date without this being shown here. Before making purchasing, import or marketing decisions, check the ANVISA search portal.

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