MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-02 for 24/26 BIPOLAR CUTTING LOOP, DIAMETER 0.35MM REF 27040GP1-S manufactured by Karl Storz Se & Co..
| Report Number | MW5087918 |
| MDR Report Key | 8768355 |
| Date Received | 2019-07-02 |
| Date of Report | 2019-06-28 |
| Date of Event | 2019-06-24 |
| Date Added to Maude | 2019-07-08 |
| 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 |
| 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 | 24/26 BIPOLAR CUTTING LOOP, DIAMETER 0.35MM |
| Generic Name | BIPOLAR ELECTRODES |
| Product Code | HIN |
| Date Received | 2019-07-02 |
| Catalog Number | REF 27040GP1-S |
| Lot Number | 37CI1943 |
| Device Availability | N |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | KARL STORZ SE & CO. |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-07-02 |