Brand Name | CODEMASTER XL+ |
Type of Device | LDD, MKJ, DQA |
Manufacturer (Section D) |
AGILENT TECHNOLOGIES, INC |
3000 minuteman rd. |
andover MA 01810 |
|
Manufacturer Contact |
phyllis
mccarthy
|
3000 minuteman rd. |
andover, MA 01810
|
9786592811
|
|
MDR Report Key | 3660502 |
MDR Text Key | 18298306 |
Report Number | 1218950-2014-00043 |
Device Sequence Number | 1 |
Product Code |
LDD
|
Combination Product (y/n) | N |
Reporter Country Code | FR |
PMA/PMN Number | K954957 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Foreign,User Facility |
Reporter Occupation |
Unknown
|
Type of Report
| Initial |
Report Date |
12/13/2013 |
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 | M1722B |
Was Device Available for Evaluation? |
Yes
|
Initial Date Manufacturer Received |
12/13/2013
|
Initial Date FDA Received | 01/06/2014 |
Was Device Evaluated by Manufacturer? |
No
|
Date Device Manufactured | 12/01/2000 |
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 |
|
|