ANVISA registration

Rennova Fill 20 Lido

Registration 80451960261. Solucao para Preenchimento Intradermico

Registration details

Registration number80451960261
Application number25351012783202581
Technical nameSolucao para Preenchimento Intradermico
Risk classIV
Published on01/06/2026
ValidityValid until 01/06/2036

Manufacturer

  • DR. KORMAN LABORATORIES LTD. ISRAEL

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