Brand Name | ACRYSOF IQ SINGLEPIECE IOL WITH ULTRASERT DELIVERY SYSTEM |
Type of Device | LENS, GUIDE, INTRAOCULAR |
Manufacturer (Section D) |
ALCON RESEARCH, LTD. - HUNTINGTON |
6065 kyle lane |
huntington WV 25702 |
|
MDR Report Key | 8194533 |
MDR Text Key | 131376227 |
Report Number | 1119421-2018-01784 |
Device Sequence Number | 1 |
Product Code |
KYB
|
Combination Product (y/n) | N |
PMA/PMN Number | P930014 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
foreign,other |
Type of Report
| Initial,Followup |
Report Date |
02/27/2019 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 12/24/2018 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Expiration Date | 12/31/2020 |
Device Model Number | AU00T0 |
Device Lot Number | 12589996 |
Was Device Available for Evaluation? |
No
|
Date Manufacturer Received | 02/26/2019 |
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Patient Sequence Number | 1 |
Treatment | PROVISC |
|
|