SUPPORT GUIDECATHETER Adverse Event — Malfunction (MDR 2029214-2020-00402)
SUPPORT GUIDECATHETER Adverse Event — Malfunction (MDR 2029214-2020-00402) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: SUPPORT GUIDECATHETER; Generic name: CATHETER, PERCUTANEOUS; Manufacturer: MICRO THERAPEUTICS, INC. DBA EV3.
| Device | SUPPORT GUIDECATHETER |
|---|---|
| Generic name | CATHETER, PERCUTANEOUS |
| Manufacturer | MICRO THERAPEUTICS, INC. DBA EV3 |
| Report number | 2029214-2020-00402 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, FOREIG |
| Narrative | IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED. |
| Source | openFDA MAUDE (device adverse events) |
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