ELEKTA INFINITY

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,other,use report with the FDA on 2019-11-01 for ELEKTA INFINITY manufactured by Elekta Ltd.

MAUDE Entry Details

Report Number9617016-2019-00007
MDR Report Key9266185
Report SourceHEALTH PROFESSIONAL,OTHER,USE
Date Received2019-11-01
Date of Report2019-11-01
Date Mfgr Received2019-10-04
Date Added to Maude2019-11-01
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
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 LTD
Manufacturer StreetLINAC HOUSE FLEMING WAY
Manufacturer CityCRAWLEY, RH109RR
Manufacturer CountryUK
Manufacturer Postal CodeRH10 9RR
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameELEKTA INFINITY
Generic NameACCELERATOR, LINEAR, MEDICAL
Product CodeIYE
Date Received2019-11-01
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerELEKTA LTD
Manufacturer AddressLINAC HOUSE FLEMING WAY CRAWLEY, RH109RR UK RH10 9RR


Patients

Patient NumberTreatmentOutcomeDate
10 2019-11-01

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