AUTOLITH TOUCH 72-00275-0

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor report with the FDA on 2020-02-05 for AUTOLITH TOUCH 72-00275-0 manufactured by Northgate Technologies Inc..

MAUDE Entry Details

Report Number0001450997-2020-00002
MDR Report Key9671809
Report SourceDISTRIBUTOR
Date Received2020-02-05
Date of Report2020-02-04
Date of Event2019-11-16
Date Mfgr Received2019-11-19
Device Manufacturer Date2019-02-01
Date Added to Maude2020-02-05
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. TODD GATTO
Manufacturer Street1591 SCOTTSDALE COURT
Manufacturer CityELGIN IL 60123
Manufacturer CountryUS
Manufacturer Postal60123
Manufacturer Phone2248562250
Manufacturer G1NORTHGATE TECHNOLOGIES INC.
Manufacturer Street1591 SCOTTSDALE COURT
Manufacturer CityELGIN IL 60123
Manufacturer CountryUS
Manufacturer Postal Code60123
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAUTOLITH TOUCH
Generic NameLITHOTRIPTER
Product CodeFFK
Date Received2020-02-05
Returned To Mfg2020-01-09
Model Number72-00275-0
Catalog Number72-00275-0
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerNORTHGATE TECHNOLOGIES INC.
Manufacturer Address1591 SCOTTSDALE COURT ELGIN IL 60123 US 60123


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-05

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