Rapid Response™ COVID-19 Antígeno Rapid Test Device
class III · Cancelled 14/02/2022
- Registration no.
- 80102512592
- Process no.
- 25351949902202049
- Status
- Cancelled 14/02/2022
- Risk class
- III
- Registration holder
- VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA CNPJ 04.718.143/0001-94 · 4,180 registrations
- Device type, manufacturer
- Not available
- Published
- 01/10/2020
- Original expiry
- 01/10/2030
- Official record
- View on ANVISA ↗