INTELLIVUE MX800 PATIENT MONITOR 865240 (MX800)

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 2020-03-16 for INTELLIVUE MX800 PATIENT MONITOR 865240 (MX800) manufactured by Philips Medical Systems.

Event Text Entries

[187546392] A follow up report will be submitted once the investigation is complete.
Patient Sequence No: 1, Text Type: N, H10


[187546393] The customer reported that the machine is hanging. No adverse event involving a patient or user was reported.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number9610816-2020-00089
MDR Report Key9834356
Report SourceFOREIGN,USER FACILITY
Date Received2020-03-16
Date of Report2020-02-17
Date Mfgr Received2020-02-17
Device Manufacturer Date2014-05-20
Date Added to Maude2020-03-16
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 ContactMS. BETTY HARRIS
Manufacturer StreetHEWLETT-PACKARD STR.2
Manufacturer CityBOEBLINGEN 71034
Manufacturer CountryGM
Manufacturer Postal71034
Manufacturer G1PHILIPS MEDICAL SYSTEMS
Manufacturer Street3000 MINUTEMAN ROAD
Manufacturer CityANDOVER MA 01810
Manufacturer CountryUS
Manufacturer Postal Code01810
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameINTELLIVUE MX800 PATIENT MONITOR
Generic NameINTELLIVUE MX800 PATIENT MONITOR
Product CodeMHX
Date Received2020-03-16
Model Number865240 (MX800)
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerPHILIPS MEDICAL SYSTEMS
Manufacturer AddressHEWLETT-PACKARD STR.2 BOEBLINGEN 71034 GM 71034


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-16

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