Brand Name | THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP TYPE S |
Type of Device | ULTRASONIC SURGICAL DEVICE |
Manufacturer (Section D) |
AOMORI OLYMPUS CO., LTD. |
2-248-1 okkonoki |
kuroishi-shi, aomori 036-0 357 |
JA 036-0357 |
|
Manufacturer (Section G) |
AOMORI OLYMPUS CO., LTD. |
2-248-1 okkonoki |
|
kuroishi-shi, aomori 036-0 357 |
JA
036-0357
|
|
Manufacturer Contact |
todd
brill
|
800 west park drive |
westborough, MA 01581
|
5082077661
|
|
MDR Report Key | 18989561 |
MDR Text Key | 338762045 |
Report Number | 9614641-2024-00775 |
Device Sequence Number | 1 |
Product Code |
GEI
|
UDI-Device Identifier | 04953170383540 |
UDI-Public | 04953170383540 |
Combination Product (y/n) | N |
Reporter Country Code | KS |
PMA/PMN Number | K211838 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Other,Foreign,User Facility,Company Representative |
Reporter Occupation |
Other
|
Type of Report
| Initial |
Report Date |
03/27/2024 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 03/27/2024 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Model Number | TB-0535FCS |
Device Lot Number | 38K04 |
Was Device Available for Evaluation? |
Device Returned to Manufacturer
|
Date Returned to Manufacturer | 03/26/2024 |
Was the Report Sent to FDA? |
No
|
Date Manufacturer Received | 02/29/2024 |
Was Device Evaluated by Manufacturer? |
No
|
Date Device Manufactured | 08/04/2023 |
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 |
|
|