ANVISA registration

Cateter de Dilatação por Balão Reewarm

Registration 81667109001. CATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA

Registration details

Registration number81667109001
Application number25351258665202011
Technical nameCATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA
Risk classII
Published on22/10/2020
ValidityIndefinite validity

Registration holder

Legal nameMICROPORT SCIENTIFIC VASCULAR BRASIL LTDA
CNPJ29.182.018/0001-33

Manufacturer

  • SHANGHAI MICROPORT ENDOVASCULAR MEDTECH (GROUP) CO., LTD. CHINA, REPÚBLICA POPULAR

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