International safety notice
Defibrillator.
Brazil / Anvisa · BRA · Jan 15, 2010
Key facts
| Title | Defibrillator. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | POWERHEART AUTOMATIC EXTERNAL DEFIBRILLATOR. |
| Manufacturer | TECNIMEDPARAMEDICS ELETROMEDICINA COMERCIAL LTDA E MEDCORP HOSPITALAR LTDA DETENTORES DE REGISTRO NO BRASIL CARDIAC SCIENCE CORPORATION FABRICANTE EUA |
| Models | 9300E, 10312210014, AED175, 9300A, 9300C, 9300P, 10265410052 |
| Date | Jan 15, 2010 |
| 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