Brand Name | ON-X CONFORM-X AORTIC PROSTHETIC HEART VALVE |
Type of Device | MECHANICAL HEART VALVE |
Manufacturer (Section D) |
ON-X LIFE TECHNOLOGIES, INC. |
1300 e anderson ln |
bldg b |
austin TX 78752 |
|
Manufacturer Contact |
walt
moeller, dir
|
1300 e anderson ln |
bldg b |
austin, TX 78752
|
5123398000
|
|
MDR Report Key | 4176963 |
MDR Text Key | 5088826 |
Report Number | 1649833-2014-00012 |
Device Sequence Number | 1 |
Product Code |
LWQ
|
Combination Product (y/n) | N |
Reporter Country Code | CA |
PMA/PMN Number | P000037 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Foreign,Distributor |
Reporter Occupation |
Not Applicable
|
Type of Report
| Initial |
Report Date |
10/10/2014 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 10/14/2014 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Lay User/Patient
|
Device Expiration Date | 06/12/2018 |
Device Model Number | ONXACE |
Device Catalogue Number | ONXACE-23 |
Other Device ID Number | 00851788001464 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
No
|
Date Manufacturer Received | 09/03/2014 |
Was Device Evaluated by Manufacturer? |
No
|
Date Device Manufactured | 05/01/2013 |
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Initial
|
Patient Sequence Number | 1 |
|
|