SYNGO RT DOSIMETRIST 2.7 SYSTEM 10568604

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-30 for SYNGO RT DOSIMETRIST 2.7 SYSTEM 10568604 manufactured by Siemens Healthcare Gmbh.

MAUDE Entry Details

Report Number3002466018-2020-21778
MDR Report Key9896963
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-30
Date of Report2020-03-02
Date of Event2020-03-02
Date Mfgr Received2020-03-02
Date Added to Maude2020-03-30
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 ContactREBECCA TUDOR
Manufacturer Street40 LIBERTY BLVD. 65-1A
Manufacturer CityMALVERN, PA
Manufacturer CountryUS
Manufacturer Phone4486484
Manufacturer G1SIEMENS HEALTHCARE GMBH
Manufacturer StreetROENTGENSTRASSE 19-21
Manufacturer CityKEMNATH, 95478
Manufacturer CountryGM
Manufacturer Postal Code95478
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSYNGO RT DOSIMETRIST 2.7 SYSTEM
Generic NameSYSTEM, PLANNING, RADIATION THERAPY TREATMENT
Product CodeMUJ
Date Received2020-03-30
Model Number10568604
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE GMBH
Manufacturer AddressROENTGENSTRASSE 19-21 KEMNATH, 95478 GM 95478


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-30

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