ANVISA registration

Fio-Guia Superstiff Pré curvado AngelGuide

Registration 81667100053. FIO GUIA CARDIOVASCULAR

Registration details

Registration number81667100053
Application number25351019218202201
Technical nameFIO GUIA CARDIOVASCULAR
Risk classIV
Published on05/09/2022
ValidityValid until 05/09/2032

Registration holder

Legal nameMICROPORT SCIENTIFIC VASCULAR BRASIL LTDA
CNPJ29.182.018/0001-33

Manufacturer

  • SHANGHAI MICROPORT CARDIOFLOW MEDTECH CO.,LTD CHINA, REPÚBLICA POPULAR

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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