Cateter Guia Aórtico Torácico Heli-FX

class II · Cancelled 06/09/2020

Registration no.
10339190690
Process no.
25351099059201707
Status
Cancelled 06/09/2020
Risk class
II
Registration holder
MEDTRONIC COMERCIAL LTDA CNPJ 01.772.798/0001-52 · 872 registrations
Device type, manufacturer
Not available
Published
02/10/2017
Original expiry
02/10/2022
Official record
View on ANVISA ↗