ANVISA registration

CARDIOVERSOR DESFIBRILADOR IMPLANTÁVEL DE CÂMARA DUPLA COND PARA RESSONÂNCIA MAGNÉTICA (FULLBody)

Registration 80224390262. DESFIBRILADOR IMPLANTÁVEL DE CÂMARA DUPLA

Registration details

Registration number80224390262
Application number25351245751201609
Technical nameDESFIBRILADOR IMPLANTÁVEL DE CÂMARA DUPLA
Risk classIV
Published on17/10/2016
ValidityExpired on 17/10/2026

Registration holder

Legal nameBIOTRONIK COMERCIAL MÉDICA LTDA.
CNPJ50.595.271/0001-05

Manufacturer

  • BIOTRONIK SE & CO. KG ALEMANHA

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