ANVISA registration

SPIROM Ti

Registration 10306840202. PARAFUSO ÓSSEO ORTOPÉDICO NÃO BIOABSORVÍVEL, ESTÉRIL

Registration details

Registration number10306840202
Application number25351287340202381
Technical namePARAFUSO ÓSSEO ORTOPÉDICO NÃO BIOABSORVÍVEL, ESTÉRIL
Risk classIII
Published on08/07/2024
ValidityValid until 08/07/2034

Registration holder

Legal namePROMEDON DO BRASIL PRODUTOS MEDICO HOSPITALARES LTDA
CNPJ00.028.682/0001-40

Manufacturer

  • PROMEDON S.A. ARGENTINA

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