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 |