MDR Report Key | 8676580 |
Report Number | COR19000279-000 |
Device Sequence Number | 1 |
Product Code |
EAP
|
Reporter Country Code | US |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Reporter Occupation |
Other
|
Type of Report
| Initial |
Report Date |
06/06/2019 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Device Operator |
Other
|
Was Device Available for Evaluation? |
No Information
|
Initial Date Manufacturer Received |
Not provided
|
Initial Date FDA Received | 06/06/2019 |
Patient Sequence Number | 1 |
|
|