MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2009-08-13 for SKYTRON 3600B * manufactured by Mizuho.
| Report Number | 1825014-2009-00006 |
| MDR Report Key | 1554080 |
| Date Received | 2009-08-13 |
| Date of Report | 2009-08-12 |
| Date Facility Aware | 2009-07-30 |
| Report Date | 2009-08-12 |
| Date Reported to FDA | 2009-08-12 |
| Date Added to Maude | 2009-12-09 |
| Event Key | 0 |
| Report Source Code | Distributor 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 | SKYTRON |
| Generic Name | SURGICAL TABLE |
| Product Code | BWN |
| Date Received | 2009-08-13 |
| Model Number | 3600B |
| Catalog Number | * |
| Lot Number | * |
| ID Number | * |
| Device Availability | N |
| Device Age | 2 YR |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | MIZUHO |
| Manufacturer Address | * TOKYO JA |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2009-08-13 |