EUCLID SYSTEMS ORTHOKERATOLOGY (OPRIFOCON A) CONTACT LENSES FOR OVERNIGHT WEAR EMERALD

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-08-15 for EUCLID SYSTEMS ORTHOKERATOLOGY (OPRIFOCON A) CONTACT LENSES FOR OVERNIGHT WEAR EMERALD manufactured by Euclid Systems Corporation.

MAUDE Entry Details

Report Number3002652243-2019-00001
MDR Report Key8899325
Date Received2019-08-15
Date of Report2019-07-16
Date of Event2019-05-21
Date Mfgr Received2019-08-12
Device Manufacturer Date2019-03-28
Date Added to Maude2019-08-15
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag0
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. SANDRA GILBERT
Manufacturer Street45472 HOLIDAY DRIVE STE 7
Manufacturer CitySTERLING VA 20166
Manufacturer CountryUS
Manufacturer Postal20166
Manufacturer Phone7034717145
Manufacturer G1EUCLID SYSTEMS CORPORATION
Manufacturer Street2776 TOWERVIEW ROAD
Manufacturer CityHERNDON VA 20171
Manufacturer CountryUS
Manufacturer Postal Code20171
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameEUCLID SYSTEMS ORTHOKERATOLOGY (OPRIFOCON A) CONTACT LENSES FOR OVERNIGHT WEAR
Generic NameEUCLID SYSTEMS ORTHOKERATOLOGY (OPRIFOCON A) CONTACT LENSES FOR OVERNIGHT WEAR
Product CodeNUU
Date Received2019-08-15
Returned To Mfg2019-07-16
Model NumberEMERALD
Lot Number18186PTC002
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerEUCLID SYSTEMS CORPORATION
Manufacturer Address2776 TOWERVIEW RD HERNDON VA 20171 US 20171


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2019-08-15

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