Brand Name | MONARCH III IOL DELIVERY SYSTEM, CARTRIDGE C |
Type of Device | FOLDERS AND INJECTORS, INTRAOCULAR LENS (IOL) |
Manufacturer (Section D) |
ALCON RESEARCH, LLC - HUNTINGTON |
6065 kyle lane |
huntington WV 25702 |
|
Manufacturer (Section G) |
ALCON RESEARCH, LLC - HUNTINGTON |
6065 kyle lane |
|
huntington WV 25702 |
|
Manufacturer Contact |
jonathan
schlech
|
6201 south freeway |
mail stop ab2-6 |
fort worth, TX 76134
|
8007579780
|
|
MDR Report Key | 17622237 |
MDR Text Key | 321920336 |
Report Number | 1119421-2023-01511 |
Device Sequence Number | 1 |
Product Code |
MSS
|
UDI-Device Identifier | 00380659777622 |
UDI-Public | 00380659777622 |
Combination Product (y/n) | N |
Reporter Country Code | BR |
PMA/PMN Number | K112977 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Foreign,Health Professional |
Reporter Occupation |
Other Health Care Professional
|
Type of Report
| Initial |
Report Date |
08/25/2023 |
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 Catalogue Number | 8065977762 |
Device Lot Number | 15585641 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Initial Date Manufacturer Received |
07/31/2023 |
Initial Date FDA Received | 08/25/2023 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 02/07/2023 |
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Initial
|
Patient Sequence Number | 1 |
Treatment | IOL LW625A; MCPHERSON FORCEPS |
Patient Outcome(s) |
Other;
|
Patient Sex | Male |