SPEEDBAND SUPERVIEW SUPER 7 Adverse Event — Malfunction (MDR 3005099803-2020-01794)
SPEEDBAND SUPERVIEW SUPER 7 Adverse Event — Malfunction (MDR 3005099803-2020-01794) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SPEEDBAND SUPERVIEW SUPER 7; Generic name: LIGATOR, ESOPHAGEAL; Manufacturer: BOSTON SCIENTIFIC CORPORATION.
| Device | SPEEDBAND SUPERVIEW SUPER 7 |
|---|---|
| Generic name | LIGATOR, ESOPHAGEAL |
| Manufacturer | BOSTON SCIENTIFIC CORPORATION |
| Report number | 3005099803-2020-01794 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | USER FACILITY |
| Narrative | (B)(4). THE DEVICE HAS NOT BEEN RECEIVED FOR ANALYSIS. SHOULD THE DEVICE BECOME AVAILABLE FOR ANALYSIS AND THERE IS ANY FURTHER RELEVANT INFORMATION, A SUPPLEMENTAL MDR WILL BE FILED. FDA REGISTRATION # MW5093631. |
| Source | openFDA MAUDE (device adverse events) |
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