ANVISA registration

Kit teste rápido de antígenos Flu A + B

Registration 81464750079. VÍRUS INFLUENZA A e B

Registration details

Registration number81464750079
Application number25351491688202028
Technical nameVÍRUS INFLUENZA A e B
Risk classIII
Published on25/01/2021
ValidityValid until 25/01/2031

Registration holder

Legal nameDomo Salute Consultoria Regulatória Ltda
CNPJ26.263.959/0001-03

Manufacturer

  • NANTONG EGENS BIOTECHNOLOGY CO., LTD. CHINA, REPÚBLICA POPULAR

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