InTRAkit com Cateter IV (Intravenoso) e Fio Guia de Nitinol

class II · Cancelled 08/12/2019

Registration no.
10339190693
Process no.
25351338425201782
Status
Cancelled 08/12/2019
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 ↗