FibroScan 530 Compact
Ultrasound device · class II · Valid
- Registration no.
- 80686360130
- Process no.
- 25351036767201702
- Status
- Valid
- Device type
- Ultrasound device (Aparelho de Ultra-Som)
- Risk class
- II
- Registration holder
- MANDALA BRASIL IMPORTACAO E DISTRIBUICAO DE PRODUTO MEDICO HOSPITALAR LTDA CNPJ 09.117.476/0001-81 · 618 registrations
- Manufacturer
- Published
- 20/03/2017
- Valid until
- No expiry (VIGENTE)
- Last updated by ANVISA
- 2026-10-12
- Official record
- View on ANVISA ↗