Brand Name | INGENIA 3.0T |
Type of Device | INGENIA 3.0T CX |
Manufacturer (Section D) |
PHILIPS ELECTRONICS NEDERLAND B.V. |
veenpluis 6 |
best 5684 PC |
NL 5684 PC |
|
Manufacturer (Section G) |
PHILIPS ELECTRONICS NEDERLAND B.V. |
veenpluis 6 |
|
best 5684 PC |
NL
5684 PC
|
|
Manufacturer Contact |
dusty
leppert
|
222 jacobs st |
cambridge, MA 02141
|
6172455900
|
|
MDR Report Key | 14958705 |
MDR Text Key | 295511521 |
Report Number | 3003768277-2022-00320 |
Device Sequence Number | 1 |
Product Code |
LNH
|
UDI-Device Identifier | 00884838068452 |
UDI-Public | 884838068452 |
Combination Product (y/n) | N |
Reporter Country Code | KS |
PMA/PMN Number | K162931 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Foreign,Health Professional,Company Representative |
Reporter Occupation |
Other Health Care Professional
|
Type of Report
| Initial,Followup |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
No
|
Device Operator |
Health Professional
|
Device Model Number | INGENIA 3.0T CX |
Device Catalogue Number | 781271 |
Was Device Available for Evaluation? |
Yes
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
05/04/2022 |
Initial Date FDA Received | 07/08/2022 |
Supplement Dates Manufacturer Received | 05/04/2022
|
Supplement Dates FDA Received | 08/10/2022
|
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 |
Patient Outcome(s) |
Other;
|
Patient Sex | Female |
|
|