Brand Name | MASTERS SERIES HEART VALSALVA AORTIC VALVES GRAFT |
Type of Device | HEART-VALVE, MECHANICAL |
Manufacturer (Section D) |
ABBOTT MEDICAL |
5050 nathan lane n |
plymouth MN 55442 |
|
Manufacturer (Section G) |
ST. JUDE MEDICAL PUERTO RICO, INC. REG#2648612 |
20 b st caguas west park |
|
caguas 00725 |
*
00725
|
|
Manufacturer Contact |
karen
krouse
|
5050 nathan lane n |
plymouth, MN 55442
|
6517565400
|
|
MDR Report Key | 16456991 |
MDR Text Key | 310405043 |
Report Number | 2135147-2023-00779 |
Device Sequence Number | 1 |
Product Code |
LWQ
|
Combination Product (y/n) | N |
Reporter Country Code | AU |
PMA/PMN Number | P810002 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Foreign,Study,Health Professional,Company Representative |
Reporter Occupation |
Physician
|
Type of Report
| Initial,Followup |
Report Date |
05/02/2023 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 02/28/2023 |
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Expiration Date | 01/31/2023 |
Device Model Number | 29VAVGJ-515 |
Device Catalogue Number | 29VAVGJ-515 |
Device Lot Number | 7806167 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Date Manufacturer Received | 04/26/2023 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 01/17/2021 |
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 |
Patient Outcome(s) |
Required Intervention;
|
Patient Age | 52 YR |
Patient Sex | Male |
Patient Weight | 92 KG |
Patient Race | White |
|
|