Brand Name | MERIT CUSTOM KIT |
Type of Device | CATHETER, INTRAVASCULAR, DIAGNOSTIC |
Manufacturer (Section D) |
MERIT MEDICAL SYSTEMS, INC. |
south jordan UT |
|
Manufacturer Contact |
paul
kennedy
|
1600 west merit pkwy. |
south jordan, UT 84095
|
8012084301
|
|
MDR Report Key | 3823843 |
MDR Text Key | 4390121 |
Report Number | 1721504-2014-00036 |
Device Sequence Number | 1 |
Product Code |
DQO
|
Combination Product (y/n) | N |
PMA/PMN Number | K913682 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Foreign,Company Representative,Distributor |
Reporter Occupation |
Not Applicable
|
Type of Report
| Initial |
Report Date |
01/24/2014 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 02/21/2014 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Expiration Date | 09/30/2016 |
Device Catalogue Number | K12-MS2666A |
Device Lot Number | H531687 |
Was Device Available for Evaluation? |
Yes
|
Date Returned to Manufacturer | 02/06/2014 |
Is the Reporter a Health Professional? |
No
|
Date Manufacturer Received | 01/24/2014 |
Was Device Evaluated by Manufacturer? |
Yes
|
Date Device Manufactured | 10/01/2013 |
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 |
|
|