Scanbody Intraoral Zfx GenTek

class II · Cancelled 16/12/2024

Registration no.
80444819009
Process no.
25351512953202361
Status
Cancelled 16/12/2024
Risk class
II
Registration holder
HIGHRIDGE MEDICAL BRASIL LTDA CNPJ 08.954.683/0001-28 · 134 registrations
Device type, manufacturer
Not available
Published
13/11/2023
Original expiry
13/11/2028
Official record
View on ANVISA ↗