MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2003-06-29 for DEL EV200 TABLE 8680R * manufactured by Del Medical Group.
[325482]
X-ray table top downward movement, on it's own, trapping pt's knee and lower extremity under table top.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | MW1028854 |
| MDR Report Key | 469511 |
| Date Received | 2003-06-29 |
| Date of Report | 2003-06-27 |
| Date of Event | 2003-06-26 |
| Date Added to Maude | 2003-07-07 |
| 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 | 0 |
| Health Professional | 3 |
| Initial Report to FDA | 0 |
| Report to FDA | 0 |
| Event Location | 3 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | DEL EV200 TABLE |
| Generic Name | * |
| Product Code | IXQ |
| Date Received | 2003-06-29 |
| Model Number | 8680R |
| Catalog Number | * |
| Lot Number | * |
| ID Number | * |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | * |
| Implant Flag | N |
| Date Removed | * |
| Device Sequence No | 1 |
| Device Event Key | 458376 |
| Manufacturer | DEL MEDICAL GROUP |
| Manufacturer Address | * * * |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2003-06-29 |