FRESHLOOK ONE-DAY CBV92013371

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign,other report with the FDA on 2020-03-20 for FRESHLOOK ONE-DAY CBV92013371 manufactured by Ciba Vision Gmbh.

MAUDE Entry Details

Report Number9610813-2020-00005
MDR Report Key9862341
Report SourceDISTRIBUTOR,FOREIGN,OTHER
Date Received2020-03-20
Date of Report2020-03-31
Date of Event2020-01-27
Date Mfgr Received2020-03-30
Device Manufacturer Date2019-07-21
Date Added to Maude2020-03-20
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 ContactMR. JONATHAN SCHLECH
Manufacturer Street6201 SOUTH FREEWAY MAIL STOP AB2-6
Manufacturer CityFORT WORTH TX 76134
Manufacturer CountryUS
Manufacturer Postal76134
Manufacturer Phone8175514979
Manufacturer G1CIBA VISION GMBH
Manufacturer StreetPOSTFACH, INDUSTRIERING 1
Manufacturer CityGROSSWALLSTADT D-63868
Manufacturer CountryGM
Manufacturer Postal CodeD-63868
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameFRESHLOOK ONE-DAY
Generic NameLENS, CONTACT, (DISPOSABLE)
Product CodeMVN
Date Received2020-03-20
Model NumberNA
Catalog NumberCBV92013371
Lot NumberN0684902
OperatorLAY USER/PATIENT
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCIBA VISION GMBH
Manufacturer AddressPOSTFACH, INDUSTRIERING 1 GROSSWALLSTADT D-63868 GM D-63868


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2020-03-20

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