ANVISA registration

Kit Instrumental para Cirurgia de Fusão Intersomática Lombar por Via Anterior

Registration 81050760097. Kit Instrumental

Registration details

Registration number81050760097
Application number25351661586201942
Technical nameKit Instrumental
Risk classI
Published on21/11/2019
ValidityIndefinite validity

Registration holder

Legal nameGUSMED DO BRASIL COMERCIO E LOCAÇÃO DE PRODUTOS MEDICOS LTDA - EPP
CNPJ19.443.457/0001-07

Manufacturer

  • NOVAX DMA S.A ARGENTINA

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