Brand Name | STORZ SIMCO DOUBLE BARRELED I/A UNIT 23G |
Type of Device | SIMCO DOUBLE BARRELED 23G I/A UNIT |
Manufacturer (Section D) |
BAUSCH & LOMB, INC. |
rochester NY 14609 |
|
Manufacturer Contact |
sharon
spencer, dir
|
50 technology |
irvine, CA 92618
|
9493985698
|
|
MDR Report Key | 4060352 |
MDR Text Key | 15104245 |
Report Number | 1920664-2014-00149 |
Device Sequence Number | 1 |
Product Code |
HNR
|
Combination Product (y/n) | N |
Reporter Country Code | US |
PMA/PMN Number | EXEMPT |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Health Professional,User Facility |
Reporter Occupation |
Physician
|
Type of Report
| Initial |
Report Date |
07/16/2014 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 08/08/2014 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Catalogue Number | E4971 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Date Manufacturer Received | 07/16/2014 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Is the Device Single Use? |
No
|
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Reuse
|
Patient Sequence Number | 1 |