ANVISA registration

Sistema Canulado para Microdebridação RhinoFlex

Registration 82209520115. Peça de mão/eletrodo eletrocirúrgico para cirurgia aberta, bipolar, de uso único

Registration details

Registration number82209520115
Application number25351068303202618
Technical namePeça de mão/eletrodo eletrocirúrgico para cirurgia aberta, bipolar, de uso único
Risk classIII
Published on29/06/2026
ValidityValid until 29/06/2036

Registration holder

Legal nameMARDEN MEDICAL LTDA
CNPJ40.220.751/0001-38

Manufacturer

  • MARDEN MEDICAL LTDA BRASIL

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