MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2019-06-28 for CRYSTALENS ACCOMMODATING IOL AT50-AO AT50AO-2450 manufactured by Bausch + Lomb.
Report Number | 0001313525-2019-00102 |
MDR Report Key | 8745500 |
Report Source | HEALTH PROFESSIONAL,USER FACI |
Date Received | 2019-06-28 |
Date of Report | 2019-06-04 |
Date of Event | 2018-06-01 |
Device Manufacturer Date | 2014-03-27 |
Date Added to Maude | 2019-06-28 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | TES PROUD |
Manufacturer Street | 1400 NORTH GOODMAN ST. |
Manufacturer City | ROCHESTER NY 14609 |
Manufacturer Country | US |
Manufacturer Postal | 14609 |
Manufacturer Phone | 5853388549 |
Manufacturer G1 | BAUSCH + LOMB |
Manufacturer Street | 21 NORTH PARK PLACE BLVD. |
Manufacturer City | CLEARWATER FL 33759 |
Manufacturer Country | US |
Manufacturer Postal Code | 33759 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CRYSTALENS ACCOMMODATING IOL |
Generic Name | LENS, INTRAOCULAR, ACCOMMODATIVE |
Product Code | NAA |
Date Received | 2019-06-28 |
Model Number | AT50-AO |
Catalog Number | AT50AO-2450 |
Lot Number | 7443716 |
Device Expiration Date | 2019-02-28 |
Operator | HEALTH PROFESSIONAL |
Device Availability | * |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BAUSCH + LOMB |
Manufacturer Address | 1400 N. GOODMAN ROCHESTER NY 14609 US 14609 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2019-06-28 |