CATETER ARTERIAL SWITCH SAFETY (FEP)

class II · Cancelled 25/08/2025

Registration no.
10290310067
Process no.
25351857996201814
Status
Cancelled 25/08/2025
Risk class
II
Registration holder
GREINER BIO-ONE BRASIL PRODUTOS MÉDICOS HOSPITALARES LTDA CNPJ 71.957.310/0001-47 · 97 registrations
Device type, manufacturer
Not available
Published
25/03/2019
Original expiry
25/03/2024
Official record
View on ANVISA ↗