Brand Name | BIOMET ULTRADRIVE PLUG PULLER ENDPIECE |
Type of Device | INSTRUMENT, SURGICAL, SONIC AND ACCESSORY/ATTACHMENT |
Manufacturer (Section D) |
|
MDR Report Key | 14695367 |
MDR Text Key | 294386946 |
Report Number | MW5110315 |
Device Sequence Number | 1 |
Product Code |
JDX
|
Combination Product (y/n) | N |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Voluntary
|
Reporter Occupation |
Risk Manager
|
Type of Report
| Initial |
Report Date |
06/10/2022 |
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
|
Was Device Available for Evaluation? |
Device Returned to Manufacturer
|
Date Returned to Manufacturer | 05/02/2022 |
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
Not provided |
Initial Date FDA Received | 06/14/2022 |
Patient Sequence Number | 1 |
|
|