MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-10-30 for FILSHIE CLIPS manufactured by Femcare Ltd..
Report Number | MW5090788 |
MDR Report Key | 9260500 |
Date Received | 2019-10-30 |
Date of Report | 2019-10-28 |
Date of Event | 2019-10-26 |
Date Added to Maude | 2019-10-31 |
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 | 3 |
Reporter Occupation | PATIENT |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 0 |
Brand Name | FILSHIE CLIPS |
Generic Name | LAPAROSCOPIC CONTRACEPTIVE TUBAL OCCLUSION DEVICE |
Product Code | KNH |
Date Received | 2019-10-30 |
Device Availability | Y |
Device Eval'ed by Mfgr | I |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | FEMCARE LTD. |
Brand Name | BREAST IMPLANTS |
Generic Name | PROSTHESIS, BREAST, NONINFLATABLE INTERNAL, SILICONE GEL-FILLED |
Product Code | FTR |
Date Received | 2019-10-30 |
Device Availability | Y |
Device Eval'ed by Mfgr | I |
Device Sequence No | 2 |
Device Event Key | 0 |
Manufacturer | UNKNOWN |
Brand Name | BREAST IMPLANTS |
Generic Name | PROSTHESIS, BREAST, NONINFLATABLE INTERNAL, SILICONE GEL-FILLED |
Product Code | FTR |
Date Received | 2019-10-30 |
Device Availability | Y |
Device Eval'ed by Mfgr | I |
Device Sequence No | 3 |
Device Event Key | 0 |
Manufacturer | UNKNOWN |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Deathisabilit | 2019-10-30 |