International safety notice
Technical name: Intra-Aortic Balloon Pump System
Brazil / Anvisa · BRA · Sep 6, 2017
Key facts
| Title | Technical name: Intra-Aortic Balloon Pump System |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Commercial name: Intra-Aortic Balloon Pump Technical name: Intra-Aortic Balloon Pump System ANVISA registration number: 10390690062 Risk class: III Affected model: CS100 intra-aortic balloon pump; |
| Manufacturer | EMPRESA DETENTORA DO REGISTRO MAQUET CARDIOPULMONARY DO BRASIL INDUSTRIA E COMERCIO LTDA CNPJ 00944324000188 AV MARGINAL DO RIBEIRÃO DOS CRISTAIS 500 CAJAMAR SP FABRICANTE DATASCOPE CORP 1300 MACARTHUR BLVD MAHWAH NJ USA 07430 ESTADOS UNIDOS DA AMÉRICA TELEFONE 19737097652 EMAIL KARENLEFEVEREGETINGECOM |
| Models | CS300, 10390690062, CS100 |
| Date | Sep 6, 2017 |
| Regulator page | anvisa.gov.br |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers 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