Brand Name | MONOPOLAR ELECTRODE |
Type of Device | STERILE MONOPOLAR ELECTRODE, 1MM |
Manufacturer (Section D) |
KARL STORZ SE & CO. KG |
dr.-karl-storz-strasse 34 |
78532 |
tuttlingen, gm |
|
Manufacturer (Section G) |
KARL STORZ SE & CO.KG |
dr.-karl-storz -strasse 34 |
78532 |
tuttlingen, gm |
|
Manufacturer Contact |
anja
fair
|
2151 e. grand avenue |
el segundo, CA 90245
|
4242118810
|
|
MDR Report Key | 13826568 |
MDR Text Key | 292979703 |
Report Number | 9610617-2022-00027 |
Device Sequence Number | 1 |
Product Code |
GEI
|
UDI-Device Identifier | 04048551392546 |
UDI-Public | 4048551392546 |
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | K972497 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
User Facility |
Reporter Occupation |
Nurse
|
Type of Report
| Initial |
Report Date |
03/17/2022 |
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? |
Yes
|
Device Operator |
Health Professional
|
Device Model Number | 11161AB-S |
Device Catalogue Number | 11161AB-S |
Was Device Available for Evaluation? |
Yes
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
02/23/2022 |
Initial Date FDA Received | 03/19/2022 |
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 |
Unknown
|
Patient Sequence Number | 1 |
|
|