Brand Name | CODEMASTER XL |
Type of Device | LDD, MKJ, DQA |
Manufacturer (Section D) |
PHILIPS MEDICAL SYSTEMS |
3000 minuteman rd. |
andover MA 01810 |
|
Manufacturer Contact |
betty
harris
|
3000 minuteman rd. |
andover, MA 01810
|
9786593311
|
|
MDR Report Key | 4231790 |
MDR Text Key | 4971699 |
Report Number | 1218950-2014-06143 |
Device Sequence Number | 1 |
Product Code |
LDD
|
Combination Product (y/n) | N |
Reporter Country Code | TW |
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 |
09/23/2014 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 10/14/2014 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
No
|
Device Operator |
Health Professional
|
Device Model Number | M1723B |
Was Device Available for Evaluation? |
Yes
|
Date Manufacturer Received | 09/23/2014 |
Was Device Evaluated by Manufacturer? |
Yes
|
Date Device Manufactured | 04/01/1999 |
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 |
|
|