ANVISA registration

COVID-19 RBD RAPID TEST

Registration 80638720175. CORONAVÍRUS

Registration details

Registration number80638720175
Application number25351040876202172
Technical nameCORONAVÍRUS
Risk classIII
Published on03/05/2021
ValidityValid until 03/05/2031

Registration holder

Legal nameDIAGNÓSTICA INDÚSTRIA E COMÉRCIO LTDA - ME
CNPJ11.462.456/0001-90

Manufacturer

  • GUANGZHOU WONDFO BIOTECH CO., LTD. CHINA, REPÚBLICA POPULAR

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Tira de Urina Biocon 10

80638720016

hCG Rapid Test Biocon

80638720017

BIOCON READER 300

80638720018

TUBOS A VACUO

80638720022

TUBOS

80638720023

ADAPTADOR DE AGULHA

80638720027

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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