ANVISA registration

INSTRUMENTAL PARA FIXADORES EXTERNOS SMART CORRECTION

Registration 80012459003. Kit Instrumental

Registration details

Registration number80012459003
Application number25351569459201266
Technical nameKit Instrumental
Risk classI
Published on11/03/2013
ValidityIndefinite validity

Registration holder

Legal nameBIOSINTESE HOSPITALAR LTDA
CNPJ01.086.229/0001-53

Manufacturing sites

  • RESPONSE ORTHO LLC ESTADOS UNIDOS DA AMÉRICA
  • TUNA MEDIKAL URUNLER TURQUIA

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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