Brand Name | UNKNOWN ZIMMER VERSYS HEAD |
Type of Device | HIP PROSTHESIS |
Manufacturer (Section D) |
ZIMMER, INC. |
p.o. box 708 |
warsaw IN 46581 0708 |
|
Manufacturer (Section G) |
ZIMMER GMBH |
|
|
winterthur |
SZ
|
|
Manufacturer Contact |
kevin
escapule
|
p.o. box 708 |
warsaw, IN 46581-0708
|
8006136131
|
|
MDR Report Key | 4898102 |
MDR Text Key | 15563925 |
Report Number | 1822565-2015-01070 |
Device Sequence Number | 1 |
Product Code |
LPH
|
Combination Product (y/n) | N |
Reporter Country Code | UK |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Foreign,Health Professional,Distributor,distributor,foreign |
Reporter Occupation |
Other
|
Type of Report
| Initial |
Report Date |
06/04/2015 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
No
|
Device Operator |
Health Professional
|
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
No
|
Initial Date Manufacturer Received |
06/04/2015
|
Initial Date FDA Received | 07/06/2015 |
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
|
Patient Sequence Number | 1 |
|
|