Brand Name | M3150 INFROMATION CENTER REV. G UPGRADE |
Type of Device | NA |
Manufacturer (Section D) |
PHILIPS MEDICAL SYSTEMS |
3000 minuteman road |
andover MA 01810 |
|
Manufacturer Contact |
robert
corning
|
3000 minuteman road |
andover, MA 01810
|
9786871501
|
|
MDR Report Key | 7609484 |
MDR Text Key | 111839640 |
Report Number | 1218950-2018-05040 |
Device Sequence Number | 1 |
Product Code |
MHX
|
Combination Product (y/n) | N |
Reporter Country Code | IT |
PMA/PMN Number | K050742 |
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 |
05/24/2018 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 06/18/2018 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Model Number | 862202 (M3150) |
Was Device Available for Evaluation? |
Yes
|
Was the Report Sent to FDA? |
No
|
Date Manufacturer Received | 05/24/2018 |
Was Device Evaluated by Manufacturer? |
Yes
|
Date Device Manufactured | 02/15/2007 |
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 |
|
|