Brand Name | MYOSURE TISSUE REMOVAL DEVICE |
Type of Device | HYSTEROSCOPE (AND ACCESSORIES) |
Manufacturer (Section D) |
HOLOGIC, INC |
250 campus drive |
marlborough MA 01752 |
|
Manufacturer (Section G) |
HOLOGIC, INC. |
250 campus drive |
|
marlborough MA 01752 |
|
Manufacturer Contact |
daniel
guevara
|
562 parkway |
coyol free zone building b24 |
san jose 20102
|
CR
20102
|
|
MDR Report Key | 18415594 |
MDR Text Key | 332497945 |
Report Number | 1222780-2023-00474 |
Device Sequence Number | 1 |
Product Code |
HIH
|
UDI-Device Identifier | 15420045505070 |
UDI-Public | (01)15420045505070(17)260907(10)23J23RD |
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K142029 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
User Facility,Company Representative |
Reporter Occupation |
Non-Healthcare Professional
|
Type of Report
| Initial |
Report Date |
12/28/2023 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 12/28/2023 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Model Number | 30-401LITE |
Device Catalogue Number | 30-401LITE |
Device Lot Number | 23J23RD |
Was Device Available for Evaluation? |
Yes
|
Date Manufacturer Received | 12/08/2023 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 09/23/2023 |
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 |