Brand Name | CONFIRM |
Type of Device | IMPLANTABLE CARDIAC MONITOR |
Manufacturer (Section D) |
ST. JUDE MEDICAL, INC. CR,D |
15900 valley view ct. |
sylmar CA 91342 |
|
Manufacturer (Section G) |
ST. JUDE MEDICAL, INC CRMD |
15900 valley view ct. |
|
sylmar CA 91342 |
|
Manufacturer Contact |
cary
lawler
|
15900 valley view ct. |
sylmar, CA 91342
|
8184932621
|
|
MDR Report Key | 4121327 |
MDR Text Key | 4949584 |
Report Number | 2017865-2014-07042 |
Device Sequence Number | 1 |
Product Code |
MXC
|
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K081365 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Health Professional,User Facility |
Reporter Occupation |
Physician
|
Type of Report
| Initial |
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 |
Health Professional
|
Device Expiration Date | 07/31/2011 |
Device Model Number | DM2100 |
Device Catalogue Number | SMTFY999 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Distributor Facility Aware Date | 01/25/2012 |
Device Age | 18 MO |
Event Location |
Hospital
|
Initial Date Manufacturer Received |
01/25/2012
|
Initial Date FDA Received | 01/13/2014 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 07/01/2010 |
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 Age | 61 YR |
|
|