Brand Name | CODEMASTER XL+ |
Type of Device | LDD, MKJ, DQA |
Manufacturer (Section D) |
PHILIPS MEDICAL SYSTEMS |
3000 minuteman rd. |
andover MA 01810 |
|
Manufacturer Contact |
denyse
murphy
|
3000 minuteman rd. |
andover, MA 01810
|
9786597844
|
|
MDR Report Key | 3880789 |
MDR Text Key | 4589004 |
Report Number | 1218950-2014-03010 |
Device Sequence Number | 1 |
Product Code |
LDD
|
Combination Product (y/n) | N |
Reporter Country Code | IT |
PMA/PMN Number | K954957 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Foreign,User Facility |
Reporter Occupation |
Other
|
Type of Report
| Initial |
Report Date |
05/07/2014 |
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
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
05/07/2014 |
Initial Date FDA Received | 05/29/2014 |
Was Device Evaluated by Manufacturer? |
No
|
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 |
|
|