ANVISA registration

VenusA-Pro Transcatheter Aortic Valve Replacement Retrievable Delivery System

Registration 80117581081. Instrumental para Válvulas Cardiacas

Registration details

Registration number80117581081
Application number25351040819202355
Technical nameInstrumental para Válvulas Cardiacas
Risk classIV
Published on16/10/2023
ValidityValid until 16/10/2033

Manufacturer

  • VENUS MEDTECH (HANGZHOU) INC 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