MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-08-05 for STAPLER GIA 60 3.8 HANDLE GIA6038S manufactured by Covidien.
| Report Number | MW5088823 |
| MDR Report Key | 8866164 |
| Date Received | 2019-08-05 |
| Date of Report | 2019-08-02 |
| Date of Event | 2019-07-21 |
| Date Added to Maude | 2019-08-06 |
| 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 | 3 |
| Reporter Occupation | RISK MANAGER |
| 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 | STAPLER GIA 60 3.8 HANDLE |
| Generic Name | STAPLER, SURGICAL |
| Product Code | GAG |
| Date Received | 2019-08-05 |
| Model Number | GIA6038S |
| Lot Number | PBG1407KX |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | COVIDIEN |
| Brand Name | STAPLER GIA 60 3.8 HANDLE |
| Generic Name | STAPLER, SURGICAL |
| Product Code | GAG |
| Date Received | 2019-08-05 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | I |
| Device Sequence No | 2 |
| Device Event Key | 0 |
| Manufacturer | COVIDIEN |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-08-05 |