ENO Adverse Event — Malfunction (MDR 1000165971-2020-00373)
ENO Adverse Event — Malfunction (MDR 1000165971-2020-00373) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ENO; Generic name: IMPLANTABLE PULSE GENERATOR, PACEMAKER (NON-CRT); Manufacturer: MICROPORT CRM S.R.L..
| Device | ENO |
|---|---|
| Generic name | IMPLANTABLE PULSE GENERATOR, PACEMAKER (NON-CRT) |
| Manufacturer | MICROPORT CRM S.R.L. |
| Report number | 1000165971-2020-00373 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | HEALTH PROFESSIONAL |
| Narrative | PRELIMINARY ANALYSIS RESULTS SHOWED THAT THE DEVICE BEHAVED AS SPECIFIED. |
| Source | openFDA MAUDE (device adverse events) |
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