RADIXACT 1060000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-01-03 for RADIXACT 1060000 manufactured by Accuray Incorporated.

MAUDE Entry Details

Report Number3003873069-2019-00013
MDR Report Key9545225
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-01-03
Date of Report2020-01-03
Date of Event2019-12-05
Date Mfgr Received2019-12-05
Date Added to Maude2020-01-03
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 ContactMR. DANIEL BIANK
Manufacturer Street1209 DEMING WAY
Manufacturer CityMADISON WI 53717
Manufacturer CountryUS
Manufacturer Postal53717
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameRADIXACT
Generic NameRADIXACT
Product CodeIYE
Date Received2020-01-03
Model Number1060000
Catalog Number1060000
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerACCURAY INCORPORATED
Manufacturer Address1209 DEMING WAY MADISON WI 53717 US 53717


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-03

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