Brand Name | ADVANTA V12 |
Type of Device | PTFE COVERED SHEET |
Manufacturer (Section D) |
ATRIUM MEDICAL CORP. |
hudson NH |
|
Manufacturer Contact |
theresa
morin, mgr
|
5 wentworth dr. |
hudson, NH 03051
|
6038801433
|
|
MDR Report Key | 3688026 |
MDR Text Key | 17569660 |
Report Number | 1219977-2014-00050 |
Device Sequence Number | 1 |
Product Code |
DSY
|
Combination Product (y/n) | N |
Reporter Country Code | MY |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Company Representative |
Reporter Occupation |
Other
|
Type of Report
| Initial |
Report Date |
02/22/2012 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 02/28/2014 |
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
No
|
Device Operator |
Health Professional
|
Device Expiration Date | 06/30/2014 |
Device Model Number | 85323 |
Device Catalogue Number | 85323 |
Device Lot Number | 10762206 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
No
|
Date Manufacturer Received | 02/22/2012 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 07/01/2011 |
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;
|
|
|