PISCES Z QUAD 3890

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 PISCES Z QUAD 3890 manufactured by Given Imaging Los Angeles Llc.

MAUDE Entry Details

Report Number3005344223-2020-00003
MDR Report Key9900281
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-30
Date of Report2020-03-30
Date of Event2020-03-09
Date Mfgr Received2020-03-10
Device Manufacturer Date2018-03-20
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 ContactAMY BEEMAN
Manufacturer Street161 CHESHIRE LANE, SUITE 100
Manufacturer CityPLYMOUTH MN 55441
Manufacturer CountryUS
Manufacturer Postal55441
Manufacturer Phone7632104064
Manufacturer G1GIVEN IMAGING LOS ANGELES LLC
Manufacturer Street5860 UPLANDER WAY
Manufacturer CityCULVER CITY CA 90230
Manufacturer CountryUS
Manufacturer Postal Code90230
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NamePISCES Z QUAD
Generic NameSTIMULATOR, SPINAL-CORD, IMPLANTED (PAIN RELIEF)
Product CodeGZB
Date Received2020-03-30
Model Number3890
Catalog Number3890
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerGIVEN IMAGING LOS ANGELES LLC
Manufacturer Address5860 UPLANDER WAY CULVER CITY CA 90230 US 90230


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-30

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