ANVISA registration

Cartucho Reagente Flex® Fósforo DIMENSION

Registration 10345161939. FÓSFORO/FOSFATO INORGÂNICO

Registration details

Registration number10345161939
Application number25351693723201455
Technical nameFÓSFORO/FOSFATO INORGÂNICO
Risk classII
Published on02/02/2015
ValidityIndefinite validity

Registration holder

Legal nameSIEMENS HEALTHCARE DIAGNÓSTICOS LTDA
CNPJ01.449.930/0001-90

Manufacturer

  • SIEMENS HEALTHACARE DIAGNOSTICS INC ESTADOS UNIDOS DA AMÉRICA

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.

Next step

Medical device registration with ANVISA

HSC manages the process from risk classification to liaising with the regulator, in Brazil and more than 40 other countries.

Speak to a specialist