International safety notice
Technical name: Catheter with Infusion Port
Brazil / Anvisa · BRA · Aug 30, 2016
Key facts
| Title | Technical name: Catheter with Infusion Port |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Secor Implantable Infusion Device with Multi-Dose Reservoir /// Technical name: Catheter with Infusion Port /// ANVISA registration number: 10175060017 /// Risk class: IV Maximum Risk /// Affected model: 09039303 - Secor Implantable Infusion Device with Multi-Dose Reservoir Affected batch numbers: See Distribution Map |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO VENTURA BIOMÉDICA LTDA CNPJ 57182230000136 AV FRANCISCO DAS CHAGAS 1100 JD MORUMBI SÃO JOSÉ DO RIO PRETOSP TELEFONE 17 21389555 EMAIL QUALIDADEVENTURAINDBR FABRICANTE VENTURA BIOMÉDICA LTDA CNPJ 57182230000136 AV FRANCISCO DAS CHAGAS 1100 JD MORUMBI SÃO JOSÉ DO RIO PRETOSP TELEFONE 17 21389555 EMAIL QUALIDADEVENTURAINDBR |
| Models | 10175060017, 09039303 |
| Date | Aug 30, 2016 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1