Brand Name | FLEX TIP PLUS EPIDURAL CATHETER |
Type of Device | CATHETER, CONDUCTION, ANESTHETIC |
Manufacturer (Section D) |
|
MDR Report Key | 12814407 |
MDR Text Key | 280935188 |
Report Number | MW5105313 |
Device Sequence Number | 2 |
Product Code |
BSO
|
Combination Product (y/n) | N |
Reporter Country Code | US |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Voluntary
|
Reporter Occupation |
Risk Manager
|
Type of Report
| Initial |
Report Date |
11/10/2021 |
3 Devices were Involved in the Event: |
1
2
3
|
1 Patient was Involved in the Event |
|
Date FDA Received | 11/12/2021 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Lot Number | 23F21C0172 |
Is the Reporter a Health Professional? |
Yes
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Patient Sequence Number | 1 |
Patient Age | 28 YR |
Patient Sex | Female |
|
|