Cateter Guia Aórtico Abdominal Heli-FX
class II · Cancelled 06/09/2020
- Registration no.
- 10339190689
- Process no.
- 25351099055201705
- Status
- Cancelled 06/09/2020
- Risk class
- II
- Registration holder
- MEDTRONIC COMERCIAL LTDA CNPJ 01.772.798/0001-52 · 872 registrations
- Device type, manufacturer
- Not available
- Published
- 02/10/2017
- Original expiry
- 02/10/2022
- Official record
- View on ANVISA ↗