Brand Name | SORIN CENTRIFUGAL PUMP CONSOLE |
Type of Device | PUMP, BLOOD, CARDIOPULMONARY BYPASS, NON-ROLLER TYPE |
Manufacturer (Section D) |
SORIN GROUP DEUTSCHLAND GMBH |
lindberghstr. 25 |
munich, 80939 |
GM 80939 |
|
Manufacturer (Section G) |
SORIN GROUP DEUTSCHLAND |
lindberghstr. 25 |
|
munich, 80939 |
GM
80939
|
|
Manufacturer Contact |
carrie
wood
|
14401 w. 65th way |
arvada, CO 80004
|
3034676461
|
|
MDR Report Key | 5240760 |
MDR Text Key | 31789178 |
Report Number | 9611109-2015-00546 |
Device Sequence Number | 1 |
Product Code |
KFM
|
Combination Product (y/n) | N |
Reporter Country Code | FR |
PMA/PMN Number | K020571 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
health professional |
Reporter Occupation |
Health Professional
|
Remedial Action |
Other |
Type of Report
| Initial,Followup |
Report Date |
10/09/2015 |
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 Model Number | 60-03-00 |
Device Catalogue Number | N/A |
Device Lot Number | N/A |
Was Device Available for Evaluation? |
Yes
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
10/09/2015 |
Initial Date FDA Received | 11/20/2015 |
Supplement Dates Manufacturer Received | Not provided
|
Supplement Dates FDA Received | 03/28/2016
|
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 10/30/2002 |
Is the Device Single Use? |
No
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Reuse
|
Patient Sequence Number | 1 |
|
|