NEUROBLATE SYSTEM Adverse Event — Malfunction (MDR 3009970070-2020-00034)
NEUROBLATE SYSTEM Adverse Event — Malfunction (MDR 3009970070-2020-00034) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: NEUROBLATE SYSTEM; Generic name: NEUROBLATE® SYSTEM; Manufacturer: MONTERIS MEDICAL.
| Device | NEUROBLATE SYSTEM |
|---|---|
| Generic name | NEUROBLATE® SYSTEM |
| Manufacturer | MONTERIS MEDICAL |
| Report number | 3009970070-2020-00034 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE |
| Narrative | DEVICE EVALUATION: THE BLUE PIXEL PHENOMENON WAS CONFIRMED DURING THE CASE. |
| Source | openFDA MAUDE (device adverse events) |
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