SOMATOM DEFINITION AS 8098027

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-10-28 for SOMATOM DEFINITION AS 8098027 manufactured by Siemens Healthcare Gmbh.

MAUDE Entry Details

Report Number3004977335-2019-02244
MDR Report Key9243951
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-10-28
Date of Report2019-10-08
Date of Event2019-10-08
Date Mfgr Received2019-10-08
Date Added to Maude2019-10-28
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 19355
Manufacturer CountryUS
Manufacturer Postal19355
Manufacturer Phone6104486484
Manufacturer G1SIEMENS HEALTHCARE GMBH
Manufacturer StreetSIEMENSTRASSE 1
Manufacturer CityFORCHHEIM, 91301
Manufacturer CountryGM
Manufacturer Postal Code91301
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSOMATOM DEFINITION AS
Generic NameSYSTEM, X-RAY, TOMOGRAPHY, COMPUTED
Product CodeJAK
Date Received2019-10-28
Model Number8098027
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE GMBH
Manufacturer AddressSIEMENSTRASSE 1 FORCHHEIM, 91301 GM 91301


Patients

Patient NumberTreatmentOutcomeDate
10 2019-10-28

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