Brand Name | LIVEWIRE¿ ELECTROPHYSIOLOGY CATHETER DUO-DECAPOLAR (20 ELECTRODES), MEDIUM CURL |
Type of Device | CATHETER, STEERABLE |
Manufacturer (Section D) |
ST. JUDE MEDICAL, INC. |
14901 deveau place |
minnetonka MN 55345 |
|
Manufacturer (Section G) |
ST. JUDE MEDICAL, INC. |
14901 deveau place |
|
minnetonka MN 55345 |
|
Manufacturer Contact |
stephanie
o' sullivan
|
5050 nathan lane north |
plymouth, MN 55442
|
6517565400
|
|
MDR Report Key | 8498164 |
MDR Text Key | 141428582 |
Report Number | 2182269-2019-00037 |
Device Sequence Number | 1 |
Product Code |
DRA
|
UDI-Device Identifier | 05414734202558 |
UDI-Public | 05414734202558 |
Combination Product (y/n) | N |
Reporter Country Code | PL |
PMA/PMN Number | K913940 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
company representative,foreig |
Reporter Occupation |
Physician
|
Type of Report
| Initial,Followup |
Report Date |
04/12/2019 |
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
|
Device Expiration Date | 03/31/2021 |
Device Model Number | 401908 |
Device Catalogue Number | 401908 |
Device Lot Number | 6393027 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Was the Report Sent to FDA? |
No
|
Initial Date Manufacturer Received |
03/19/2019 |
Initial Date FDA Received | 04/09/2019 |
Supplement Dates Manufacturer Received | 03/19/2019
|
Supplement Dates FDA Received | 04/12/2019
|
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 04/23/2018 |
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;
|
|
|