Fio-guia para Trato Urinário de Uso Único
General-purpose guidewire, non-vascular · class II · Valid
- Registration no.
- 83210069012
- Process no.
- 25351128776202681
- Status
- Valid
- Device type
- General-purpose guidewire, non-vascular (FIO GUIA DE USO GERAL, NÃO VASCULAR)
- Risk class
- II
- Registration holder
- KODA MEDITEC BRASIL LTDA CNPJ 57.516.989/0001-08 · 12 registrations
- Manufacturer
- Published
- 10/08/2026
- Valid until
- No expiry (VIGENTE)
- Last updated by ANVISA
- 2026-10-12
- Official record
- View on ANVISA ↗