VISCOAT OPHTHALMIC VISCOSURGICAL DEVICE 8065183975

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2020-02-25 for VISCOAT OPHTHALMIC VISCOSURGICAL DEVICE 8065183975 manufactured by Alcon - Couvreur N.v./alcon - Belgium.

MAUDE Entry Details

Report Number3002037047-2020-00003
MDR Report Key9752316
Report SourceHEALTH PROFESSIONAL
Date Received2020-02-25
Date of Report2020-02-25
Date of Event2020-02-12
Date Mfgr Received2020-02-12
Date Added to Maude2020-02-25
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 ContactMR. JONATHAN SCHLECH
Manufacturer Street6201 SOUTH FREEWAY MAIL STOP AB2-6
Manufacturer CityFORT WORTH TX 76134
Manufacturer CountryUS
Manufacturer Postal76134
Manufacturer Phone8175514979
Manufacturer G1ALCON - COUVREUR N.V./ALCON - BELGIUM
Manufacturer StreetRIJKSWEG 14
Manufacturer CityPUURS B-2870
Manufacturer CountryBE
Manufacturer Postal CodeB-2870
Single Use3
Previous Use Code3
Removal Correction NumberNA
Event Type3
Type of Report3

Device Details

Brand NameVISCOAT OPHTHALMIC VISCOSURGICAL DEVICE
Generic NameAID, SURGICAL, VISCOELASTIC
Product CodeLZP
Date Received2020-02-25
Model NumberNA
Catalog Number8065183975
Lot Number028148
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerALCON - COUVREUR N.V./ALCON - BELGIUM
Manufacturer AddressRIJKSWEG 14 PUURS B-2870 BE B-2870


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-25

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