CRYSTALENS ACCOMMODATING IOL AT50AO AT50AO-1750

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2019-07-17 for CRYSTALENS ACCOMMODATING IOL AT50AO AT50AO-1750 manufactured by Bausch + Lomb.

MAUDE Entry Details

Report Number0001313525-2019-00114
MDR Report Key8799446
Report SourceCONSUMER
Date Received2019-07-17
Date of Report2018-11-15
Device Manufacturer Date2015-07-28
Date Added to Maude2019-07-17
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. TES PROUD
Manufacturer Street1400 NORTH GOODMAN STREET
Manufacturer CityROCHESTER NY 14609
Manufacturer CountryUS
Manufacturer Postal14609
Manufacturer Phone5853388549
Manufacturer G1BAUSCH + LOMB
Manufacturer Street21 NORTH PARK PLACE BLVD.
Manufacturer CityCLEARWATER FL 33759
Manufacturer CountryUS
Manufacturer Postal Code33759
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCRYSTALENS ACCOMMODATING IOL
Generic NameLENS, INTRAOCULAR, ACCOMMODATIVE
Product CodeNAA
Date Received2019-07-17
Model NumberAT50AO
Catalog NumberAT50AO-1750
Lot Number7558202
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBAUSCH + LOMB
Manufacturer Address1400 NORTH GOODMAN STREET ROCHESTER NY 14609 US 14609


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-07-17

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