ANVISA registration

DS-EIA-FSH

Registration 80189860307. HORMÔNIO FOLÍCULO ESTIMULANTE (FSH)

Registration details

Registration number80189860307
Application number25351387912201552
Technical nameHORMÔNIO FOLÍCULO ESTIMULANTE (FSH)
Risk classII
Published on21/09/2015
ValidityIndefinite validity

Registration holder

Legal nameANFLA PRODUTOS PARA DIAGNOSTICOS LABORATORIAL LTDA
CNPJ05.774.798/0001-42

Manufacturer

  • RPC DIAGNOSTIC SYSTEMS RÚSSIA (FEDERAÇÃO RUSSA)

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