MONACO

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,o report with the FDA on 2018-01-24 for MONACO manufactured by Elekta Inc.

Event Text Entries

[98294033] The investigation was completed by conducting a thorough evaluation of the product and the reported information. The issue was determined to be a defect in the product and will be fixed in a later version.
Patient Sequence No: 1, Text Type: N, H10


[98294034] The customer reported that monaco will display the incorrect mu for a 3d plan. Based on the available information there has been no mistreatment.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1937649-2018-00005
MDR Report Key7215480
Report SourceFOREIGN,HEALTH PROFESSIONAL,O
Date Received2018-01-24
Date of Report2018-01-24
Date Mfgr Received2018-01-11
Date Added to Maude2018-01-24
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationPHYSICIST
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactPMS
Manufacturer StreetLINAC HOUSE FLEMING WAY
Manufacturer CityCRAWLEY, WEST SUSSEX RH109RR
Manufacturer CountryUK
Manufacturer PostalRH10 9RR
Manufacturer G1ELEKTA INC.
Manufacturer Street13723 RIVERPORT DRIVE SUITE 100
Manufacturer CityMARYLAND HEIGHTS MO 63043
Manufacturer CountryUS
Manufacturer Postal Code63043
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameMONACO
Generic NameSYSTEM,PLANNING,RADIATION THERAPY TREATMENT
Product CodeMUJ
Date Received2018-01-24
OperatorPHYSICIST
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerELEKTA INC
Manufacturer Address13723 RIVERPORT DRIVE SUITE 100 MARYLAND HEIGHTS MO 63043 US 63043


Patients

Patient NumberTreatmentOutcomeDate
10 2018-01-24

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