Brand Name | BED, MANUAL |
Type of Device | BED, MANUAL |
Manufacturer (Section D) |
|
MDR Report Key | 17530950 |
MDR Text Key | 321134590 |
Report Number | MW5137866 |
Device Sequence Number | 1 |
Product Code |
FNJ
|
Combination Product (y/n) | N |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Voluntary
|
Reporter Occupation |
Other
|
Type of Report
| Initial |
Report Date |
08/20/2018 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 08/12/2023 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
No
|
Device Model Number | GENDRON 750LB BED |
Patient Sequence Number | 1 |
|
|