MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2012-08-27 for * 331693 manufactured by B.braun Medical.
| Report Number | 2772366 |
| MDR Report Key | 2772366 |
| Date Received | 2012-08-27 |
| Date of Report | 2012-08-27 |
| Date of Event | 2012-04-03 |
| Report Date | 2012-08-27 |
| Date Reported to FDA | 2012-08-27 |
| Date Added to Maude | 2012-10-04 |
| 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 | 3 |
| 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 | * |
| Generic Name | CONTINUOUS NERVE BLOCK SET |
| Product Code | BXN |
| Date Received | 2012-08-27 |
| Model Number | * |
| Catalog Number | 331693 |
| Lot Number | * |
| ID Number | * |
| Device Availability | N |
| Device Age | 1 DY |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | B.BRAUN MEDICAL |
| Manufacturer Address | 901 MARCON BOULEVARD ALLENTOWN PA 18109 US 18109 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2012-08-27 |