FIO GUIA HIBRID

class IV · Cancelled 20/06/2021

Registration no.
80065320160
Process no.
25351334421201020
Status
Cancelled 20/06/2021
Risk class
IV
Registration holder
CMS PRODUTOS HOSPITALARES LTDA CNPJ 03.301.390/0001-28 · 314 registrations
Device type, manufacturer
Not available
Published
31/05/2011
Original expiry
31/05/2026
Official record
View on ANVISA ↗