Fibroureterorenoscópio
class II · Cancelled 26/08/2019
- Registration no.
- 10371280041
- Process no.
- 25351669578201494
- Status
- Cancelled 26/08/2019
- Risk class
- II
- Registration holder
- PENTAX MEDICAL BRASIL MATERIAIS E EQUIPAMENTOS LTDA - EPP CNPJ 01.716.863/0001-22 · 52 registrations
- Device type, manufacturer
- Not available
- Published
- 02/02/2015
- Original expiry
- 02/02/2020
- Official record
- View on ANVISA ↗