ANVISA registration

FIO GUIA HIBRID

Registration 81936210017. FIO GUIA CARDIOVASCULAR

Registration details

Registration number81936210017
Application number25351040746202130
Technical nameFIO GUIA CARDIOVASCULAR
Risk classIV
Published on22/03/2021
ValidityValid until 31/05/2036

Registration holder

Legal nameBALT BRASIL PRODUTOS MEDICOS LTDA
CNPJ12.236.355/0002-44

Manufacturer

  • BALT EXTRUSION SAS FRANÇA

Other registrations held by BALT BRASIL PRODUTOS MEDICOS LTDAview all

CATETER HIPERSELETIVO SONIC

81936210000

CATETER GUIA CORAIL

81936210001

CATETER HIPERSELETIVO VASCO

81936210002

BALAO DESTACAVEL BALT

81936210003

STENT LEO+BABY

81936210004

STENT SILK VISTA BABY

81936210005

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