BIS 186-1046

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign report with the FDA on 2019-11-12 for BIS 186-1046 manufactured by Aspect Medical.

MAUDE Entry Details

Report Number2936999-2019-00936
MDR Report Key9313475
Report SourceFOREIGN
Date Received2019-11-12
Date of Report2019-11-12
Date Mfgr Received2019-10-28
Device Manufacturer Date2015-03-19
Date Added to Maude2019-11-12
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 G1ASPECT MEDICAL
Manufacturer Street1 UPLAND RD
Manufacturer CityNORWOOD MA 02062
Manufacturer CountryUS
Manufacturer Postal Code02062
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBIS
Generic NameINDEX-GENERATING ELECTROENCEPHALOGRAPH SOFTWARE
Product CodeOLW
Date Received2019-11-12
Returned To Mfg2019-11-04
Model Number186-1046
Catalog Number186-1046
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerASPECT MEDICAL
Manufacturer Address1 UPLAND RD NORWOOD MA 02062 US 02062


Patients

Patient NumberTreatmentOutcomeDate
10 2019-11-12

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