FIO GUIA HIBRID
Cardiovascular guidewire · class IV · Until 31/05/2036
- Registration no.
- 81936210017
- Process no.
- 25351040746202130
- Status
- Until 31/05/2036
- Device type
- Cardiovascular guidewire (FIO GUIA CARDIOVASCULAR)
- Risk class
- IV
- Registration holder
- BALT BRASIL PRODUTOS MEDICOS LTDA CNPJ 12.236.355/0002-44 · 35 registrations
- Manufacturer
- Published
- 22/03/2021
- Valid until
- 31/05/2036
- Last updated by ANVISA
- 2026-10-12
- Official record
- View on ANVISA ↗