Brand Name | CLAREON IOL WITH THE AUTONOME DELIVERY SYSTEM |
Type of Device | INTRAOCULAR LENS |
Manufacturer (Section D) |
ALCON LABORATORIES IRELAND LTD. |
cork business&technology park |
model farm road |
cork 00000 |
EI 00000 |
|
Manufacturer (Section G) |
ALCON LABORATORIES IRELAND LTD. |
cork business&technology park |
model farm road |
cork 00000 |
EI
00000
|
|
Manufacturer Contact |
jonathan
schlech
|
6201 south freeway |
mail stop ab2-6 |
fort worth, TX 76134
|
8007579780
|
|
MDR Report Key | 14771390 |
MDR Text Key | 294499575 |
Report Number | 9612169-2022-00287 |
Device Sequence Number | 1 |
Product Code |
HQL
|
UDI-Device Identifier | 00380652393805 |
UDI-Public | 00380652393805 |
Combination Product (y/n) | N |
Reporter Country Code | AS |
PMA/PMN Number | P190018 |
Number of Events Reported | 1 |
Summary Report (Y/N) | N |
Report Source |
Manufacturer
|
Source Type |
Foreign,Health Professional,Company Representative |
Reporter Occupation |
Physician
|
Type of Report
| Initial |
Report Date |
06/22/2022 |
1 Device was Involved in the Event |
|
1 Patient was Involved in the Event |
|
Date FDA Received | 06/22/2022 |
Is this an Adverse Event Report? |
No
|
Is this a Product Problem Report? |
Yes
|
Device Operator |
Health Professional
|
Device Model Number | CNA0T0 |
Device Lot Number | 25273625 |
Was Device Available for Evaluation? |
No
|
Is the Reporter a Health Professional? |
Yes
|
Date Manufacturer Received | 03/30/2022 |
Was Device Evaluated by Manufacturer? |
Device Not Returned to Manufacturer
|
Date Device Manufactured | 09/22/2021 |
Is This a Reprocessed and Reused Single-Use Device? |
No
|
Type of Device Usage |
Initial
|
Patient Sequence Number | 1 |