ANVISA registration

QIASYMPHONY AS

Registration 10322259012. Instrumento para preparo e processamento de amostras fase pré-analítica

Registration details

Registration number10322259012
Application number25351261763201427
Technical nameInstrumento para preparo e processamento de amostras fase pré-analítica
Risk classI
Published on03/11/2014
ValidityIndefinite validity

Registration holder

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

Manufacturer

  • QIAGEN GMBH ALEMANHA

Other registrations held by QIAGEN BIOTECNOLOGIA BRASIL LTDA.view all

DIGENE CAPTURA HIBRIDA HPV

10322250001

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

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.

Next step

Medical device registration with ANVISA

HSC manages the process from risk classification to liaising with the regulator, in Brazil and more than 40 other countries.

Speak to a specialist