International safety notice
Implantable Pulse Generator Pacemaker.
Brazil / Anvisa · BRA · Apr 25, 2011
Key facts
| Title | Implantable Pulse Generator Pacemaker. |
|---|---|
| Regulator | Brazil / Anvisa |
| Country | BRA |
| Brand | Kappa Medtronic Series 900 Pacemaker; |
| Manufacturer | MEDTRONIC COMERCIAL |
| Models | 10339190277, 10339190170, 10339190278, 10339190183 |
| Date | Apr 25, 2011 |
| 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