Brand Name | MOXI SA MAX |
Type of Device | MATTRESS, AIR FLOTATION, ALTERNATING PRESSURE |
Manufacturer (Section D) |
|
MDR Report Key | 17536811 |
MDR Text Key | 321347813 |
Report Number | MW5143695 |
Device Sequence Number | 1 |
Product Code |
FNM
|
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 |
03/06/2017 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
No
|
Device Model Number | MOXI LAL 36X80 MATTRESS, MOXI APL CONTROL UNIT |
Device Lot Number | SASHORTMATT, SA MAX |
Initial Date Manufacturer Received |
Not provided |
Initial Date FDA Received | 08/12/2023 |
Patient Sequence Number | 1 |
Patient Age | 78 YR |
|
|