EVIS EXERA DUODENOVIDEOSCOPE Adverse Event — Malfunction (MDR 8010047-2020-02407)
EVIS EXERA DUODENOVIDEOSCOPE Adverse Event — Malfunction (MDR 8010047-2020-02407) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: EVIS EXERA DUODENOVIDEOSCOPE; Generic name: DUODENOVIDEOSCOPE; Manufacturer: OLYMPUS MEDICAL SYSTEMS CORP..
| Device | EVIS EXERA DUODENOVIDEOSCOPE |
|---|---|
| Generic name | DUODENOVIDEOSCOPE |
| Manufacturer | OLYMPUS MEDICAL SYSTEMS CORP. |
| Report number | 8010047-2020-02407 |
| Event type | Malfunction |
| Product problem | Y |
| Date received | 2020-04-28 |
| Report source | FOREIGN, USER FACILITY |
| Narrative | THE SUBJECT DEVICE IN THIS REPORT HAS NOT BEEN RETURNED TO OMSC FOR EVALUATION. THE EXACT CAUSE OF THE REPORTED EVENT COULD NOT BE CONCLUSIVELY DETERMINED AT THIS TIME. IF ADDITIONAL INFORMATION BECOMES AVAILABLE, THIS REPORT WILL BE SUPPLEMENTED. |
| Source | openFDA MAUDE (device adverse events) |
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