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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: PHILIPS NORTH AMERICA LLC SURESIGNS VM 8 PATIENT MONITOR
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PHILIPS NORTH AMERICA LLC SURESIGNS VM 8 PATIENT MONITOR Back to Search Results
Model Number 863066
Medical Device Problem Code Fitting Problem (2183)
Health Effect - Clinical Code No Clinical Signs, Symptoms or Conditions (4582)
Date of Event 08/23/2022
Type of Reportable Event Malfunction
Event or Problem Description
It was reported to philips that suresigns vm 8 patient monitor nibp button and alarm buttons were not functioning.The device was not in use at the time the issue was discovered.
 
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Brand Name
SURESIGNS VM 8 PATIENT MONITOR
Common Device Name
SURESIGNS VM 8 PATIENT MONITOR
Manufacturer (Section D)
PHILIPS NORTH AMERICA LLC
3000 minuteman road
andover MA 01810
Manufacturer (Section G)
PHILIPS NORTH AMERICA LLC
3000 minuteman road
andover MA 01810
Manufacturer Contact
jeanne ahearn
222 jacobs st
cambridge, MA 02141
6172455900
MDR Report Key15326236
Report Number1218950-2022-00850
Device Sequence Number15074310
Product Code MHX
UDI-Device Identifier00884838000063
UDI-Public00884838000063
Combination Product (Y/N)N
Initial Reporter CountryIN
PMA/510(K) Number
K123900
Number of Events Summarized1
Summary Report (Y/N)N
Serviced by Third Party (Y/N)N
Reporter Type Manufacturer
Report Source Foreign,User Facility
Initial Reporter Occupation Other
Type of Report Initial
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Operator of Device Health Professional
Device Model Number863066
Device Catalogue Number863066
Was Device Available for Evaluation? Yes
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 08/23/2022
Initial Report FDA Received Date08/31/2022
Was Device Evaluated by Manufacturer? (Y/N) Yes
Date Device Manufactured02/20/2014
Is the Device Labeled for Single Use? (Y/N) No
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)		 No
Usage of Device Reuse
Patient Sequence Number1
Patient SexUnknown
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