STREAMLAB ANALYTICAL WORKCELL 10444806

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2020-03-17 for STREAMLAB ANALYTICAL WORKCELL 10444806 manufactured by Siemens Healthcare Diagnostics Inc..

MAUDE Entry Details

Report Number2517506-2020-00104
MDR Report Key9845395
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2020-03-17
Date of Report2020-03-17
Date of Event2020-02-22
Date Mfgr Received2020-02-22
Date Added to Maude2020-03-17
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 ContactROLANDO HUALPA
Manufacturer Street511 BENEDICT AVENUE
Manufacturer CityTARRYTOWN, NY
Manufacturer CountryUS
Manufacturer Phone5242963
Manufacturer G1INPECO S.P.A
Manufacturer StreetVIA GIVOLETTO 15 REGISTRATION #: 3005509212
Manufacturer CityVAL DELLA TORRE, TORINO 10040
Manufacturer CountryIT
Manufacturer Postal Code10040
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSTREAMLAB ANALYTICAL WORKCELL
Generic NameSTREAMLAB ANALYTICAL WORKCELL
Product CodeLGX
Date Received2020-03-17
Model NumberSTREAMLAB ANALYTICAL WORKCELL
Catalog Number10444806
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE DIAGNOSTICS INC.
Manufacturer Address500 GBC DRIVE PO BOX 6101 NEWARK, DE US


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-17

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