GUIDEWIRE 3.2 THREAD-TIP L215 SST Adverse Event — Malfunction (MDR 8030965-2020-03156)
GUIDEWIRE 3.2 THREAD-TIP L215 SST Adverse Event — Malfunction (MDR 8030965-2020-03156) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: GUIDEWIRE 3.2 THREAD-TIP L215 SST; Generic name: GUIDE; Manufacturer: OBERDORF SYNTHES PRODUKTIONS GMBH.
| Device | GUIDEWIRE 3.2 THREAD-TIP L215 SST |
|---|---|
| Generic name | GUIDE |
| Manufacturer | OBERDORF SYNTHES PRODUKTIONS GMBH |
| Report number | 8030965-2020-03156 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | COMPANY REPRESENTATIVE, FOREIG |
| Narrative | WITHOUT A LOT NUMBER, THE DEVICE HISTORY RECORDS REVIEW COULD NOT BE COMPLETED AS NO PRODUCT WAS RECEIVED. THE INVESTIGATION COULD NOT BE COMPLETED, NO PRODUCT WAS RECEIVED; NO CONCLUSION COULD BE DRAWN AT THE TIME OF FILING THIS REPORT. DEVICE WAS USED FOR TREATMENT, NOT DIAGNOSIS. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS AP |
| Source | openFDA MAUDE (device adverse events) |
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