ANVISA registration

Kit Canula para Anuloplastia percutânea Dirigível Orthoplus +

Registration 82209520056. Eletrodo eletrocirúrgico endoscópico, bipolar, uso único

Registration details

Registration number82209520056
Application number25351018156202554
Technical nameEletrodo eletrocirúrgico endoscópico, bipolar, uso único
Risk classIII
Published on26/05/2025
ValidityValid until 26/05/2035

Registration holder

Legal nameMARDEN MEDICAL LTDA
CNPJ40.220.751/0001-38

Manufacturer

  • MARDEN MEDICAL LTDA BRASIL

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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