MICROWAVE ENDOMETRIAL ABLATION (MEA) SYSTEM Adverse Event — Injury (MDR 9710493-2008-00001)
MICROWAVE ENDOMETRIAL ABLATION (MEA) SYSTEM Adverse Event — Injury (MDR 9710493-2008-00001) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: MICROWAVE ENDOMETRIAL ABLATION (MEA) SYSTEM; Generic name: MICROWAVE ENDOMETRIAL ABLATION DEVICE; Manufacturer: MICROSULIA MEDICAL LTD..
| Device | MICROWAVE ENDOMETRIAL ABLATION (MEA) SYSTEM |
|---|---|
| Generic name | MICROWAVE ENDOMETRIAL ABLATION DEVICE |
| Manufacturer | MICROSULIA MEDICAL LTD. |
| Report number | 9710493-2008-00001 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-21 |
| Report source | Foreign, Health Professional |
| Narrative | PT WAS TREATED WITH A REUSABLE APPLICATOR. USER SUSPECTED FORWARD ADVANCEMENT OF THE APPLICATOR AND ABORTED THE TREATMENT. LAPAROSCOPY CONFIRMED UTERINE PERFORATION AND INJURY TO BOWEL. CORRECTIVE SURGERY PERFORMED. |
| Source | openFDA MAUDE (device adverse events) |
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