SYNGO X-WORKPLACE 10281299

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2019-09-26 for SYNGO X-WORKPLACE 10281299 manufactured by Siemens Healthcare Gmbh.

MAUDE Entry Details

Report Number3004977335-2019-98201
MDR Report Key9122206
Report SourceUSER FACILITY
Date Received2019-09-26
Date of Report2019-09-04
Date of Event2019-09-04
Date Mfgr Received2019-09-04
Date Added to Maude2019-09-26
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 ContactMEREDITH ADAMS
Manufacturer Street40 LIBERTY BLVD. 65-1A
Manufacturer CityMALVERN PA 19355
Manufacturer CountryUS
Manufacturer Postal19355
Manufacturer Phone6104486461
Manufacturer G1SIEMENS HEALTHCARE GMBH
Manufacturer StreetSIEMENSTRASSE 1
Manufacturer CityFORCCHEIM, 91301
Manufacturer CountryGM
Manufacturer Postal Code91301
Single Use3
Remedial ActionIN
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSYNGO X-WORKPLACE
Generic NameSYSTEM, IMAGE PROCESSING, RADIOLOGICAL
Product CodeLLZ
Date Received2019-09-26
Model Number10281299
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE GMBH
Manufacturer AddressSIEMENSTRASSE 1 FORCCHEIM, 91301 GM 91301


Patients

Patient NumberTreatmentOutcomeDate
10 2019-09-26

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