Brand Name | SYMPHION |
Type of Device | INSUFFLATOR, HYSTEROSCOPIC, FLUID, CLOSED-LOOP RECIRCULATION WITH CUTTER-COAGULA |
Manufacturer (Section D) |
BOSTON SCIENTIFIC CORPORATION |
300 boston scientific way |
marlborough MA 01752 |
|
Manufacturer (Section G) |
NORTECH SYSTEM INC |
nw 7791 |
1450 |
minneapolis MN 55485 |
|
Manufacturer Contact |
carole
morley
|
300 boston scientific way |
marlborough, MA 01752
|
5086834015
|
|
MDR Report Key | 10874856 |
MDR Text Key | 220958641 |
Report Number | 3005099803-2020-05217 |
Device Sequence Number | 1 |
Product Code |
PGT
|
UDI-Device Identifier | 08714729863717 |
UDI-Public | 08714729863717 |
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K141848 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
company representative,health |
Reporter Occupation |
Physician
|
Type of Report
| Initial |
Report Date |
11/20/2020 |
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 Expiration Date | 08/03/2021 |
Device Model Number | FG-0202 |
Device Catalogue Number | 74052 |
Device Lot Number | 0083170582 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
10/26/2020
|
Initial Date FDA Received | 11/20/2020 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 08/03/2020 |
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 |