ANVISA registration

FIO GUIA PTFE FLEX P

Registration 81042210017. Fio Guia

Registration details

Registration number81042210017
Application number25351852610201870
Technical nameFio Guia
Risk classII
Published on15/07/2019
ValidityIndefinite validity

Registration holder

Legal namePorto71 Importação e Exportação Ltda
CNPJ17.035.479/0001-02

Manufacturer

  • LAVI DISPOSITIVOS MÉDICOS UNIPESSOAL LTDA PORTUGAL

Other registrations held by Porto71 Importação e Exportação Ltdaview all

Cateter para Retirada de Calculos TRITON

81042210001

Fio Guia Hidrofílico Titan

81042210002

Kit Renal Amplatz

81042210003

EVACUADOR DE ELLICK

81042210004

KIT DE DILATADORES RENAIS AMPLATZ

81042210005

BAINHA DE ACESSO URETERAL FLEX PASS

81042210006

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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