Brand Name | ACESSA PROVU HANDPIECE |
Type of Device | COAGULATOR, LAPAROSCOPIC, UNIPOLAR (AND ACCESORIES) |
Manufacturer (Section D) |
HOLOGIC, INC |
250 campus drive |
marlborough MA 01752 |
|
Manufacturer (Section G) |
HOLOGIC, INC. |
250 campus drive |
|
marlborough MA 01752 |
|
Manufacturer Contact |
ariel
lafuente
|
562 parkway |
coyol free zone building b24 |
san jose 20102
|
CR
20102
|
|
MDR Report Key | 17821492 |
MDR Text Key | 324304426 |
Report Number | 1222780-2023-00357 |
Device Sequence Number | 1 |
Product Code |
HFG
|
UDI-Device Identifier | 15420045515246 |
UDI-Public | (01)15420045515246(17)250124(10)C00018520 |
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K181124 |
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 |
09/26/2023 |
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 | 7300 |
Device Lot Number | C00018520 |
Was Device Available for Evaluation? |
No
|
Initial Date Manufacturer Received |
09/01/2023 |
Initial Date FDA Received | 09/26/2023 |
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 |
Patient Outcome(s) |
Required Intervention;
Other;
|
Patient Sex | Female |