CATETER PARA ANGIOPLASTIA TRANSLUMINAL PERCUTANEO (PTA) SLEEK
Peripheral angioplasty balloon catheter · class III · Until 05/05/2028
- Registration no.
- 81576620015
- Process no.
- 25351102953202357
- Status
- Until 05/05/2028
- Device type
- Peripheral angioplasty balloon catheter (CATETER BALÃO PARA ANGIOPLASTIA PERIFÉRICA)
- Risk class
- III
- Registration holder
- CORDIS MEDICAL BRASIL LTDA CNPJ 27.548.227/0001-22 · 69 registrations
- Manufacturer
- Published
- 06/03/2023
- Valid until
- 05/05/2028
- Last updated by ANVISA
- 2026-10-12
- Official record
- View on ANVISA ↗