ANVISA registration

SHUNT INTRACORONÁRIO

Registration 10166360035. Dispositivo Para Anastomose

Registration details

Registration number10166360035
Application number25351264937201046
Technical nameDispositivo Para Anastomose
Risk classIV
Published on11/07/2011
ValidityValid until 11/07/2036

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.

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