ANVISA registration

HI-TORQUE COMMAND GUIDE WIRE

Registration 80146501828. FIO GUIA CARDIOVASCULAR

Registration details

Registration number80146501828
Application number25351640930201221
Technical nameFIO GUIA CARDIOVASCULAR
Risk classII
Published on01/04/2013
ValidityIndefinite validity

Registration holder

Legal nameABBOTT LABORATORIOS DO BRASIL LTDA
CNPJ56.998.701/0001-16

Manufacturer

  • ABBOTT MEDICAL ESTADOS UNIDOS DA AMÉRICA

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SONDA NASOENTERAL FLEXIFLO 8Fr-10Fr-12Fr

10055310572

CN-Free Hemoglobin Reagent

10055310721

DILUENT/SHEATH CD Sapphire and CD Ruby

10055310743

WBC REAGENT PART B

10055310785

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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