VIEWMATE? Z ULTRASOUND CONSOLE WBATTERY ZS3 H701336

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 2019-11-06 for VIEWMATE? Z ULTRASOUND CONSOLE WBATTERY ZS3 H701336 manufactured by Zonare Medical Systems, Inc.

MAUDE Entry Details

Report Number3004189859-2019-00003
MDR Report Key9284089
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-11-06
Date of Report2019-11-06
Date of Event2019-10-24
Date Mfgr Received2019-10-24
Device Manufacturer Date2015-10-05
Date Added to Maude2019-11-06
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 ContactSTEPHANIE O' SULLIVAN
Manufacturer Street5050 NATHAN LANE NORTH
Manufacturer CityPLYMOUTH MN 55442
Manufacturer CountryUS
Manufacturer Postal55442
Manufacturer Phone6517565400
Manufacturer G1ZONARE MEDICAL SYSTEMS, INC
Manufacturer Street420 NORTH BERNARDO AVENUE
Manufacturer CityMOUNTAIN VIEW CA 94043
Manufacturer CountryUS
Manufacturer Postal Code94043
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVIEWMATE? Z ULTRASOUND CONSOLE WBATTERY ZS3
Generic NameULTRASONIC PULSED DOPPLER IMAGING SYSTEM
Product CodeIYN
Date Received2019-11-06
Model NumberH701336
Catalog NumberH701336
Lot Number5254117
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerZONARE MEDICAL SYSTEMS, INC
Manufacturer Address420 NORTH BERNARDO AVENUE MOUNTAIN VIEW CA 94043 US 94043


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-11-06

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