ANVISA registration

FIO GUIA RADIOFOCUS GLIDEWIRE TERUMO

Registration 80012280073. FIO GUIA CARDIOVASCULAR

Registration details

Registration number80012280073
Application number25351176974200527
Technical nameFIO GUIA CARDIOVASCULAR
Risk classIV
Published on26/09/2005
ValidityValid until 26/09/2035

Registration holder

Legal nameTERUMO MEDICAL DO BRASIL LTDA.
CNPJ03.129.105/0001-33

Manufacturer

  • TERUMO CORPORATION JAPÃO

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.

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