ANVISA registration

FIO-GUIA NITINOL

Registration 80603600012. Fio Guia

Registration details

Registration number80603600012
Application number25351602792201147
Technical nameFio Guia
Risk classII
Published on19/12/2011
ValidityIndefinite validity

Registration holder

Legal nameHUMMER DO BRASIL COMERCIAL IMP E EXP. DE EQUIPS HOSPITALARES LTDA
CNPJ09.553.187/0001-25

Manufacturer

  • Marflow AG - Medical Equipment SUÍÇA

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

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