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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: REMOTE DIAGNOSTIC TECHNOLOGIES LTD. TEMPUS PRO; MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)

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REMOTE DIAGNOSTIC TECHNOLOGIES LTD. TEMPUS PRO; MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS) Back to Search Results
Model Number 00-1024-R
Device Problem Failure to Power Up (1476)
Patient Problem No Clinical Signs, Symptoms or Conditions (4582)
Event Date 06/01/2023
Event Type  malfunction  
Event Description
It has been reported to philips that the device charging port is not working.
 
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Brand Name
TEMPUS PRO
Type of Device
MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS)
Manufacturer (Section D)
REMOTE DIAGNOSTIC TECHNOLOGIES LTD.
ascent 1, aerospace centre
aerospace boulevard
farnborough GU14 6XW
UK  GU14 6XW
Manufacturer (Section G)
REMOTE DIAGNOSTIC TECHNOLOGIES LTD.
ascent 1, aerospace centre
aerospace boulevard
farnborough GU14 6XW
UK   GU14 6XW
Manufacturer Contact
jon yard
ascent 1, aerospace centre
aerospace boulevard
farnborough GU14 -6XW
UK   GU14 6XW
MDR Report Key17171444
MDR Text Key317771574
Report Number3003832357-2023-00390
Device Sequence Number1
Product Code MHX
UDI-Device Identifier05060472441027
UDI-Public05060472441027
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K201746
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type Health Professional
Reporter Occupation Other
Type of Report Initial,Followup
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received06/21/2023
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Model Number00-1024-R
Device Catalogue Number989706000051
Was Device Available for Evaluation? Yes
Is the Reporter a Health Professional? No
Date Manufacturer Received07/13/2023
Was Device Evaluated by Manufacturer? No
Is the Device Single Use? No
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Reuse
Patient Sequence Number1
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