INTELLISPHERE EVENT MANAGEMENT 866030

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2018-08-21 for INTELLISPHERE EVENT MANAGEMENT 866030 manufactured by Philips Medical Systems.

Event Text Entries

[117700403] A follow up report will be submitted once the investigation is complete.
Patient Sequence No: 1, Text Type: N, H10


[117700404] The customer reported that the emergency display no longer shows any alarms. There was no patient incident.
Patient Sequence No: 1, Text Type: D, B5


[140019324]
Patient Sequence No: 1, Text Type: N, H10


MAUDE Entry Details

Report Number1218950-2018-06734
MDR Report Key7800521
Report SourceFOREIGN,HEALTH PROFESSIONAL,U
Date Received2018-08-21
Date of Report2018-07-25
Date Mfgr Received2018-07-25
Device Manufacturer Date2018-06-11
Date Added to Maude2018-08-21
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
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
Manufacturer ContactMS. BETTY HARRIS
Manufacturer Street3000 MINUTEMAN ROAD
Manufacturer CityANDOVER MA 01810
Manufacturer CountryUS
Manufacturer Postal01810
Manufacturer Phone9786871501
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameINTELLISPHERE EVENT MANAGEMENT
Generic NameCOMMUNICATION SYSTEM
Product CodeMSX
Date Received2018-08-21
Model Number866030
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerPHILIPS MEDICAL SYSTEMS
Manufacturer Address3000 MINUTEMAN ROAD ANDOVER MA 01810 US 01810


Patients

Patient NumberTreatmentOutcomeDate
10 2018-08-21

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