International safety notice
Technical name: Balao Intra-Aortic Pump System
Brazil / Anvisa · BRA · Apr 3, 2017
Key facts
| Title | Technical name: Balao Intra-Aortic Pump System |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: INTRA-AORTIC BALLOON PUMP Technical name: Balao Intra-Aortic Pump System ANVISA registration number: 10390690062 Risk class: III Affected model: CARDIOSAVE Hybrid; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO MAQUET CARDIOPULMONARY DO BRASIL INDUSTRIA E COMERCIO LTDA ENDEREÇO AV MARGINAL DO RIBEIRAO DOS CRISTAIS 500 TELEFONE 11 26087426 FABRICANTE MAQUET CARDIOPULMONARY DO BRASIL INDUSTRIA E COMERCIO LTDA 00944324000188 AV MARGINAL DO RIBEIRAO DOS CRISTAIS 500 CAJAMAR SP 11 26087426 DATASCOPE CORP 1300 MACARTHUR BLVD MAHWAH NJ USA 07430 |
| Models | 150468904PE, 10390690062, 150470604PE |
| Date | Apr 3, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
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