Cobas® TaqScreen Cadaveric Specimen Diluent Kit

class I · Cancelled 18/02/2026

Registration no.
10287410911
Process no.
25351602698201039
Status
Cancelled 18/02/2026
Risk class
I
Registration holder
ROCHE DIAGNÓSTICA BRASIL LTDA CNPJ 30.280.358/0001-86 · 1,784 registrations
Device type, manufacturer
Not available
Published
30/11/2010
Original expiry
30/11/2020
Official record
View on ANVISA ↗