ANVISA registration

DIGENE CAPTURA HIBRIDA HPV

Registration 10322250001. PAPILOMAVÍRUS HUMANO (HPV)

Registration details

Registration number10322250001
Application number250000200339701
Technical namePAPILOMAVÍRUS HUMANO (HPV)
Risk classIII
Published on28/04/1998
ValidityValid until 28/04/2033

Registration holder

Legal nameQIAGEN BIOTECNOLOGIA BRASIL LTDA.
CNPJ01.334.250/0001-20

Manufacturer

  • QIAGEN ESTADOS UNIDOS DA AMÉRICA

Other registrations held by QIAGEN BIOTECNOLOGIA BRASIL LTDA.view all

CAPTURA HIBRIDA PARA CT/GC

10322250007

QUIMIOLUMINÔMETRO DML 2000 DIGENE SISTEMA LUMINÔMETRO EM MICROPLACA

10322250012

KIT DE COLETA DOS ESPÉCIMES

10322250018

DIGENE CAPTURA HIBRIDA 2 HPV ALTO RISCO

10322250019

Dispositivo de Conversão de Amostras hc2

10322250021

PyroMark Q24 Validation Oligo

10322250041

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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