Kit Cânula Percutânea Probe Ultrassônica

class II · Cancelled 19/08/2024

Registration no.
82209529164
Process no.
25351111305202391
Status
Cancelled 19/08/2024
Risk class
II
Registration holder
MARDEN MEDICAL LTDA CNPJ 40.220.751/0001-38 · 509 registrations
Device type, manufacturer
Not available
Published
06/03/2023
Original expiry
06/03/2028
Official record
View on ANVISA ↗