BENEVISION CENTRAL MONITORING SYSTEM

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2020-01-30 for BENEVISION CENTRAL MONITORING SYSTEM manufactured by Shenzhen Mindray Bio-medical Electronics Co., Ltd.

MAUDE Entry Details

Report Number2221819-2020-00002
MDR Report Key9649188
Date Received2020-01-30
Date of Report2020-01-06
Date of Event2020-01-04
Date Facility Aware2020-01-06
Report Date2020-01-30
Date Reported to Mfgr2020-01-30
Date Added to Maude2020-01-30
Event Key0
Report Source CodeDistributor report
Manufacturer LinkN
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationBIOMEDICAL ENGINEER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameBENEVISION CENTRAL MONITORING SYSTEM
Generic NameBENEVISION
Product CodeMSX
Date Received2020-01-30
Model NumberBENEVISION CENTRAL MONITORING SYSTEM
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerSHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD
Manufacturer Address1203 NANHUAN AVENUE GUANGMING GUANGMING DISTRICT SHENZHEN, 518106 CH 518106


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-30

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