Agulha Hipodérmica Prolife

class II · Cancelled 01/08/2022

Registration no.
80261410056
Process no.
25351007959201251
Status
Cancelled 01/08/2022
Risk class
II
Registration holder
REMED PHARMA LTDA -ME CNPJ 06.985.581/0001-44 · 59 registrations
Device type, manufacturer
Not available
Published
28/05/2012
Original expiry
28/05/2017
Official record
View on ANVISA ↗