MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2012-05-04 for LAPAROSCOPIC TENNACULUM 33310UM * manufactured by Karl Storz.
| Report Number | 2572406 |
| MDR Report Key | 2572406 |
| Date Received | 2012-05-04 |
| Date of Report | 2012-05-04 |
| Date of Event | 2012-04-30 |
| Report Date | 2012-05-04 |
| Date Reported to FDA | 2012-05-04 |
| Date Added to Maude | 2012-05-14 |
| Event Key | 0 |
| Report Source Code | User Facility 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 | RISK MANAGER |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | LAPAROSCOPIC TENNACULUM |
| Generic Name | TENACULUM |
| Product Code | HDC |
| Date Received | 2012-05-04 |
| Model Number | 33310UM |
| Catalog Number | * |
| Lot Number | * |
| ID Number | * |
| Operator | PHYSICIAN |
| Device Availability | Y |
| Device Age | 3 YR |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | KARL STORZ |
| Manufacturer Address | 2151 EAST GRAND AVENUE EL SEGUNDO CA 90245 US 90245 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2012-05-04 |