CRYSTALENS ACCOMMODATING IOL AT50-AO AT50AO-2450

MAUDE Adverse Event Report

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.

MAUDE Entry Details

Report Number0001313525-2019-00102
MDR Report Key8745500
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2019-06-28
Date of Report2019-06-04
Date of Event2018-06-01
Device Manufacturer Date2014-03-27
Date Added to Maude2019-06-28
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactTES PROUD
Manufacturer Street1400 NORTH GOODMAN ST.
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 Received2019-06-28
Model NumberAT50-AO
Catalog NumberAT50AO-2450
Lot Number7443716
Device Expiration Date2019-02-28
OperatorHEALTH PROFESSIONAL
Device Availability*
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerBAUSCH + LOMB
Manufacturer Address1400 N. GOODMAN ROCHESTER NY 14609 US 14609


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-06-28

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