Brand Name | PRESSURE MONITORING KIT WITH TRUWAVE DISPOSABLE PRESSURE TRANSDUCER |
Type of Device | TRANSDUCER, PRESSURE, CATHETER TIP |
Manufacturer (Section D) |
EDWARDS LIFESCIENCES DR |
parque industrial de itabo |
carr. sanchez km 18.5 |
haina, san cristobal |
DR |
|
Manufacturer (Section G) |
EDWARDS LIFESCIENCES DR |
parque industrial de itabo |
carr. sanchez km 18.5 |
haina, san cristobal |
DR
|
|
Manufacturer Contact |
lynn
selawski
|
1 edwards way |
irvine, CA 92614
|
9497564386
|
|
MDR Report Key | 5368336 |
MDR Text Key | 36471965 |
Report Number | 2015691-2016-00156 |
Device Sequence Number | 1 |
Product Code |
DXO
|
Combination Product (y/n) | N |
Reporter Country Code | CH |
PMA/PMN Number | K925638 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
company representative,foreig |
Reporter Occupation |
Health Professional
|
Type of Report
| Initial,Followup |
Report Date |
12/24/2015 |
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 | 01/13/2017 |
Device Model Number | PX260 |
Device Lot Number | 59963877 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
12/24/2015
|
Initial Date FDA Received | 01/14/2016 |
Supplement Dates Manufacturer Received | Not provided
|
Supplement Dates FDA Received | 03/07/2016
|
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 01/14/2015 |
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 |