Brand Name | STONE CRUSHING FORCEPS, SGL. ACTION JAWS |
Type of Device | STONE CRUSHING FORCEPS, SGL. ACTION JAWS |
Manufacturer (Section D) |
KARL STORZ SE & CO. KG |
dr.-karl-storz-strasse 34 |
tuttlingen, 78532 |
GM 78532 |
|
Manufacturer (Section G) |
KARL STORZ SE & CO. KG |
dr.-karl-storz-strasse 34 |
|
tuttlingen, 78532 |
GM
78532
|
|
Manufacturer Contact |
anja
fair
|
2151 e grand ave. |
el segundo, CA 90245
|
4242188247
|
|
MDR Report Key | 18722366 |
MDR Text Key | 335593972 |
Report Number | 9610617-2024-00039 |
Device Sequence Number | 1 |
Product Code |
OCZ
|
Combination Product (y/n) | N |
Reporter Country Code | CA |
PMA/PMN Number | K950434 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Other,Health Professional,Company Representative |
Reporter Occupation |
Nurse
|
Type of Report
| Initial |
Report Date |
02/16/2024 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 02/16/2024 |
Is this an Adverse Event Report? |
Yes
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Model Number | 27074B |
Device Catalogue Number | 27074B |
Is the Reporter a Health Professional? |
Yes
|
Date Manufacturer Received | 01/24/2024 |
Was Device Evaluated by Manufacturer? |
No
|
Is the Device Single Use? |
No
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Unknown
|
Patient Sequence Number | 1 |
Patient Outcome(s) |
Required Intervention;
Other;
|
Patient Age | 58 YR |
Patient Sex | Male |
Patient Weight | 120 KG |