ANVISA registration

Família Alinity m STI

Registration 80146502213. PARÂMETROS COMBINADOS NO MESMO PRODUTO - CLASSE III

Registration details

Registration number80146502213
Application number25351321061201977
Technical namePARÂMETROS COMBINADOS NO MESMO PRODUTO - CLASSE III
Risk classIII
Published on17/06/2019
ValidityValid until 17/06/2029

Registration holder

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

Manufacturer

  • ABBOTT MOLECULAR INC ESTADOS UNIDOS DA AMÉRICA

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SONDA NASOENTERAL FLEXIFLO 8Fr-10Fr-12Fr

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DILUENT/SHEATH CD Sapphire and CD Ruby

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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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