Brand Name | QUART ARTERIAL FILTER, MODEL HBF 140 |
Type of Device | FILTER, BLOOD, CPB, ARTERIAL LINE |
Manufacturer (Section D) |
MAQUET CARDIOPULMONARY AG |
kehler strasse 31 |
rastatt, 7643 7 |
GM 76437 |
|
Manufacturer (Section G) |
MAQUET CARDIOPULMONARY AG |
kehler strasse 31 |
|
rastatt, 7643 7 |
GM
76437
|
|
Manufacturer Contact |
tina
evancho
|
maquet medical system, usa |
45 barbour pond drive |
wayne, NJ 07470
|
9737097265
|
|
MDR Report Key | 4282859 |
MDR Text Key | 5030998 |
Report Number | 8010762-2014-00475 |
Device Sequence Number | 1 |
Product Code |
DTM
|
Combination Product (y/n) | N |
Reporter Country Code | JA |
PMA/PMN Number | K001787 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Foreign,Health Professional,User Facility,Company Representative |
Reporter Occupation |
Other
|
Type of Report
| Initial |
Report Date |
10/10/2012 |
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 |
Other
|
Device Expiration Date | 01/31/2014 |
Device Model Number | HBF-140 J |
Device Catalogue Number | 70103.1617 |
Device Lot Number | 70076441 |
Was Device Available for Evaluation? |
Device Returned to Manufacturer
|
Date Returned to Manufacturer | 10/19/2012 |
Was the Report Sent to FDA? |
No
|
Distributor Facility Aware Date | 10/10/2012 |
Device Age | 9 MO |
Event Location |
Hospital
|
Date Report to Manufacturer | 10/10/2012 |
Initial Date Manufacturer Received |
10/10/2012 |
Initial Date FDA Received | 11/27/2014 |
Was Device Evaluated by Manufacturer? |
Yes
|
Date Device Manufactured | 01/01/2012 |
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 |
|
|