BIS 186-0195-DM

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,user facility report with the FDA on 2019-11-22 for BIS 186-0195-DM manufactured by Jabil Circuit Singapore Pte Ltd.

MAUDE Entry Details

Report Number2936999-2019-00967
MDR Report Key9364849
Report SourceFOREIGN,USER FACILITY
Date Received2019-11-22
Date of Report2019-11-22
Date Mfgr Received2019-10-29
Date Added to Maude2019-11-22
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactAVI KLUGER
Manufacturer Street5920 LONGBOW DRIVE
Manufacturer CityBOULDER CO 80301
Manufacturer CountryUS
Manufacturer Postal80301
Manufacturer Phone3035306582
Manufacturer G1JABIL CIRCUIT SINGAPORE PTE LTD
Manufacturer Street16 TAMPINES CRESCENT
Manufacturer CitySINGAPORE,SG 528604
Manufacturer CountrySG
Manufacturer Postal Code528604
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBIS
Generic NameINDEX-GENERATING ELECTROENCEPHALOGRAPH SOFTWARE
Product CodeOLW
Date Received2019-11-22
Returned To Mfg2019-11-04
Model Number186-0195-DM
Catalog Number186-0195-DM
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerJABIL CIRCUIT SINGAPORE PTE LTD
Manufacturer Address16 TAMPINES CRESCENT SINGAPORE,SG 528604 SG 528604


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-11-22

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