MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2013-12-02 for FILSHIE CLIPS manufactured by .
[4043523]
Filshie clips in 2006. Since then have experienced ptls symptoms; hormonal imbalance resulting in shorter cycle, heavier periods and stabbing pains.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW5033203 |
| MDR Report Key | 3501894 |
| Date Received | 2013-12-02 |
| Date of Report | 2013-11-27 |
| Date Added to Maude | 2013-12-06 |
| Event Key | 0 |
| Report Source Code | Voluntary report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 0 |
| Reporter Occupation | PATIENT |
| Health Professional | 0 |
| Initial Report to FDA | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | FILSHIE CLIPS |
| Generic Name | FILSHIE CLIPS |
| Product Code | HGB |
| Date Received | 2013-12-02 |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Deathisabilit | 2013-12-02 |