ANVISA registration

Radifocus Fio Guia M não vascular

Registration 10430319069. FIO GUIA DE USO GERAL, NÃO VASCULAR

Registration details

Registration number10430319069
Application number25351040512202192
Technical nameFIO GUIA DE USO GERAL, NÃO VASCULAR
Risk classII
Published on18/02/2021
ValidityIndefinite validity

Registration holder

Legal nameCOLOPLAST DO BRASIL LTDA.
CNPJ02.794.555/0003-40

Manufacturer

  • TERUMO EUROPA N.V. BÉLGICA

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