DUAL CHAMBER TEMPORARY PACEMAKER Adverse Event — Injury (MDR 3004593495-2020-00482)
DUAL CHAMBER TEMPORARY PACEMAKER Adverse Event — Injury (MDR 3004593495-2020-00482) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: DUAL CHAMBER TEMPORARY PACEMAKER; Generic name: PULSE-GENERATOR, PACEMAKER, EXTERNAL; Manufacturer: PLEXUS MANUFACTURING SDN. BHD.
| Device | DUAL CHAMBER TEMPORARY PACEMAKER |
|---|---|
| Generic name | PULSE-GENERATOR, PACEMAKER, EXTERNAL |
| Manufacturer | PLEXUS MANUFACTURING SDN. BHD |
| Report number | 3004593495-2020-00482 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | HEALTH PROFESSIONAL |
| Narrative | IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED. |
| Source | openFDA MAUDE (device adverse events) |
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