LIGHTTRAIL SINGLE USE M0068F64640 69267

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-30 for LIGHTTRAIL SINGLE USE M0068F64640 69267 manufactured by Boston Scientific Corporation.

MAUDE Entry Details

Report Number3005099803-2020-01283
MDR Report Key9897240
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-30
Date of Report2020-03-30
Date of Event2020-02-01
Date Mfgr Received2020-03-11
Device Manufacturer Date2019-10-30
Date Added to Maude2020-03-30
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 ContactCAROLE MORLEY
Manufacturer Street300 BOSTON SCIENTIFIC WAY
Manufacturer CityMARLBOROUGH MA 01752
Manufacturer CountryUS
Manufacturer Postal01752
Manufacturer Phone5086834015
Manufacturer G1BOSTON SCIENTIFIC CORPORATION
Manufacturer StreetMODEL FARM ROAD CORK
Manufacturer CityCORK IRELAND
Manufacturer CountryEI
Manufacturer Postal CodeIRELAND
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameLIGHTTRAIL SINGLE USE
Generic NamePOWERED LASER SURGICAL INSTRUMENT
Product CodeGEX
Date Received2020-03-30
Returned To Mfg2020-03-03
Model NumberM0068F64640
Catalog Number69267
Lot Number0024681763
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerBOSTON SCIENTIFIC CORPORATION
Manufacturer Address300 BOSTON SCIENTIFIC WAY MARLBOROUGH MA 01752 US 01752


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-30

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