Brand Name | MATTRESS, AIR FLOTATION, ALTERNATING PRESSURE |
Type of Device | MATTRESS, AIR FLOTATION, ALTERNATING PRESSURE |
Manufacturer (Section D) |
|
MDR Report Key | 17528673 |
MDR Text Key | 321051974 |
Report Number | MW5135603 |
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 |
07/25/2018 |
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 | TRIDIEN APL 48X80 MATTRESS, TRIDIEN STAT 5000 AP BARI CU |
Device Catalogue Number | 5000C, 3001016 |
Initial Date Manufacturer Received |
Not provided
|
Initial Date FDA Received | 08/12/2023 |
Patient Sequence Number | 1 |
|
|