ANVISA registration

DISPOSITIVO DE REGULAGEM PARA VÁLVULA PROGRAMÁVEL SPHERA PRO

Registration 10166369001. Equipamento de Diagnóstico em Neurologia

Registration details

Registration number10166369001
Application number25351710777201418
Technical nameEquipamento de Diagnóstico em Neurologia
Risk classI
Published on08/12/2014
ValidityIndefinite validity

Registration holder

Legal nameHP BIOPROTESES LTDA
CNPJ54.801.196/0001-42

Manufacturer

  • HP BIOPROTESES LTDA BRASIL

Other registrations held by HP BIOPROTESES LTDAview all

SHUNT LOMBO PERITONEAL HPBIO

10166360025

DERIVAÇÃO PARA HIDROCEFALIA SPHERA

10166360026

DERIVAÇÃO PARA HIDROCEFALIA SPHERA DUO

10166360029

RESERVATÓRIO CEREBRAIS

10166360030

CATETER ATRIAL

10166360031

CÂNULA DE PERFUSÃO CORONÁRIA

10166360032

Source: ANVISA

Source: ANVISA open data, medical device file, updated daily. The public database provides registration validity, rather than registration status: this registration may have been cancelled before its expiry date without this being shown here. Before making purchasing, import or marketing decisions, check the ANVISA search portal.

Next step

Medical device registration with ANVISA

HSC manages the process from risk classification to liaising with the regulator, in Brazil and more than 40 other countries.

Speak to a specialist