CRYSTALENS ACCOMMODATING IOL AO1UV AO1UV-2075

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2019-09-13 for CRYSTALENS ACCOMMODATING IOL AO1UV AO1UV-2075 manufactured by Bausch + Lomb.

MAUDE Entry Details

Report Number0001313525-2019-00145
MDR Report Key9050478
Report SourceUSER FACILITY
Date Received2019-09-13
Date of Report2019-08-14
Date of Event2019-08-13
Report Date2005-01-01
Date Reported to FDA2005-01-01
Date Reported to Mfgr2005-01-10
Date Mfgr Received2019-10-11
Device Manufacturer Date2016-02-23
Date Added to Maude2019-09-13
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. STEPHANIE ANASTASIOU
Manufacturer Street21 N PARK BLVD
Manufacturer CityCLEARWATER FL 33759
Manufacturer CountryUS
Manufacturer Postal33759
Manufacturer Phone7277246659
Manufacturer G1BAUSCH + LOMB
Manufacturer Street21 NORTH PARK PLACE BLVD.
Manufacturer CityCLEARWATER FL 33759
Manufacturer CountryUS
Manufacturer Postal Code33759
Single Use0
Previous Use Code0
Event Type3
Type of Report3

Device Details

Brand NameCRYSTALENS ACCOMMODATING IOL
Generic NameLENS, INTRAOCULAR, ACCOMMODATIVE
Product CodeNAA
Date Received2019-09-13
Model NumberAO1UV
Catalog NumberAO1UV-2075
Lot Number7643514
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Sequence No1
Device Event Key0
ManufacturerBAUSCH + LOMB
Manufacturer Address1400 NORTH GOODMAN ST ROCHESTER NY 14609 US 14609


Patients

Patient NumberTreatmentOutcomeDate
101. Other; 2. Required No Informationntervention 2019-09-13

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