Brand Name | TX2 TISSUE REMOVAL SYSTEM - MICROTIP |
Type of Device | INSTRUMENT, ULTRASONIC SURGICAL |
Manufacturer (Section D) |
TENEX HEALTH, INC. |
26902 vista terrace |
lake forest CA 92630 8123 |
|
Manufacturer (Section G) |
TENEX HEALTH, INC. |
26902 vista terrace |
|
lake forest CA 92630 |
|
Manufacturer Contact |
david
vancelette
|
26902 vista terrace |
lake forest, CA 92630
|
9492388220
|
|
MDR Report Key | 17761181 |
MDR Text Key | 323818952 |
Report Number | 1000135560-2023-00037 |
Device Sequence Number | 1 |
Product Code |
LFL
|
UDI-Device Identifier | 00857156006154 |
UDI-Public | (01)00857156006154 |
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K153299 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Distributor |
Reporter Occupation |
Non-Healthcare Professional
|
Type of Report
| Initial |
Report Date |
09/15/2023 |
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 | 554-2003-001 |
Device Catalogue Number | 554-2003-001 |
Was Device Available for Evaluation? |
No
|
Initial Date Manufacturer Received |
08/21/2023
|
Initial Date FDA Received | 09/15/2023 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Is the Device Single Use? |
Yes
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Initial
|
Patient Sequence Number | 1 |