Brand Name | NOVASURE |
Type of Device | DEVICE, THERMAL ABLATION, ENDOMETRIAL |
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 jos[?], alajuela 20102- CRI
|
CS
20102 CRI
|
|
MDR Report Key | 11694340 |
MDR Text Key | 246808094 |
Report Number | 1222780-2021-00075 |
Device Sequence Number | 1 |
Product Code |
MNB
|
UDI-Device Identifier | 15420045508224 |
UDI-Public | (01)15420045508224(10)20A31RG(17)220228 |
Combination Product (y/n) | N |
Reporter Country Code | IS |
PMA/PMN Number | P010013 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
company representative,foreig |
Reporter Occupation |
Non-Healthcare Professional
|
Type of Report
| Initial |
Report Date |
04/20/2021 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 04/20/2021 |
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
No
|
Device Operator |
Health Professional
|
Device Expiration Date | 02/28/2022 |
Device Model Number | 2013 |
Device Catalogue Number | NS2013 |
Device Lot Number | 20A31RG |
Was Device Available for Evaluation? |
No
|
Date Manufacturer Received | 04/03/2021 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 01/31/2020 |
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) |
Other;
|