Brand Name | SOMATOM FORCE |
Type of Device | SYSTEM, X-RAY, TOMOGRAPHY, COMPUTED |
Manufacturer (Section D) |
SIEMENS HEALTHCARE GMBH |
siemensstrasse 1~or |
rittigfeld 1 |
forchheim 91301 |
GM 91301 |
|
Manufacturer (Section G) |
SIEMENS HEALTHCARE GMBH |
siemensstrasse 1~or |
rittigfeld 1 |
forchheim 91301 |
GM
91301
|
|
Manufacturer Contact |
meredith
adams
|
40 liberty blvd. |
malvern, PA 19355
|
4843231631
|
|
MDR Report Key | 18490872 |
MDR Text Key | 332603229 |
Report Number | 3004977335-2024-00001 |
Device Sequence Number | 1 |
Product Code |
JAK
|
UDI-Device Identifier | 04056869006956 |
UDI-Public | 04056869006956 |
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K230421 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Company Representative |
Reporter Occupation |
Other
|
Type of Report
| Initial,Followup |
Report Date |
02/16/2024 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 01/11/2024 |
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
No
|
Device Operator |
Health Professional
|
Device Model Number | 10742326 |
Device Catalogue Number | 10742326 |
Was Device Available for Evaluation? |
Yes
|
Is the Reporter a Health Professional? |
No
|
Date Manufacturer Received | 02/16/2024 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Is the Device Single Use? |
No
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
A
|
Patient Sequence Number | 1 |
Patient Outcome(s) |
Other;
|
|
|