Brand Name | OPTIPAC-S 60 REFOB BN CMT R |
Type of Device | BONE CEMENT, ANTIBIOTIC |
Manufacturer (Section D) |
BIOMET FRANCE S.A.R.L. |
plateau de lautagne bp75 |
valence cedex 26903 |
FR 26903 |
|
Manufacturer (Section G) |
BIOMET FRANCE S.A.R.L. |
plateau de lautagne bp75 |
|
valence cedex 26903 |
FR
26903
|
|
Manufacturer Contact |
elisabeth
plane
|
plateau de lautagne bp75 |
valence cedex 26903
|
FR
26903
|
0334757591
|
|
MDR Report Key | 6051649 |
MDR Text Key | 58198403 |
Report Number | 3006946279-2016-00392 |
Device Sequence Number | 1 |
Product Code |
MBB
|
Combination Product (y/n) | N |
Reporter Country Code | UK |
PMA/PMN Number | PNI |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
company representative,foreig |
Reporter Occupation |
Other
|
Type of Report
| Initial |
Report Date |
09/26/2016 |
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? |
Yes
|
Device Operator |
Physician
|
Device Model Number | N/A |
Device Catalogue Number | 4711500396-1 |
Other Device ID Number | N/A |
Was Device Available for Evaluation? |
No
|
Initial Date Manufacturer Received |
09/26/2016 |
Initial Date FDA Received | 10/24/2016 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Is the Device Single Use? |
Yes
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Initial
|
Removal/Correction Number | N/A |
Patient Sequence Number | 1 |