Brand Name | EUFLEXXA INJ 10MG/ML |
Type of Device | EUFLEXXA INJ 10MG/ML |
MDR Report Key | 6199341 |
MDR Text Key | 63195406 |
Report Number | MW5066867 |
Device Sequence Number | 2 |
Product Code |
MOZ
|
UDI-Device Identifier | 55566410001 |
UDI-Public | 55566410001 |
Reporter Country Code | US |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Voluntary
|
Reporter Occupation |
Pharmacist
|
Type of Report
| Initial |
Report Date |
12/19/2016 |
2 Devices were Involved in the Event: |
1
2
|
1 Patient was Involved in the Event |
|
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
No
|
Device Operator |
No Information
|
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
Not provided |
Initial Date FDA Received | 12/19/2016 |
Type of Device Usage |
N
|
Patient Sequence Number | 1 |
Patient Age | 58 YR |
|
|