Agulha Hipodérmica Prolife com Dispositivo de Segurança
class II · Cancelled 01/08/2022
- Registration no.
- 80261410057
- Process no.
- 25351007974201259
- Status
- Cancelled 01/08/2022
- Risk class
- II
- Registration holder
- REMED PHARMA LTDA -ME CNPJ 06.985.581/0001-44 · 59 registrations
- Device type, manufacturer
- Not available
- Published
- 28/05/2012
- Original expiry
- 28/05/2017
- Official record
- View on ANVISA ↗