STREAMLAB ANALYTICAL WORKCELL 10444806

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-19 for STREAMLAB ANALYTICAL WORKCELL 10444806 manufactured by Siemens Healthcare Diagnostics Inc..

MAUDE Entry Details

Report Number2517506-2019-00293
MDR Report Key8808111
Date Received2019-07-19
Date of Report2019-09-16
Date of Event2019-05-27
Date Mfgr Received2019-07-23
Date Added to Maude2019-07-19
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 ContactMR. MIR KHAN
Manufacturer Street511 BENEDICT AVENUE
Manufacturer CityTARRYTOWN NY 10591
Manufacturer CountryUS
Manufacturer Postal10591
Manufacturer Phone9145243074
Manufacturer G1INPECO S.P.A
Manufacturer StreetVIA GIVOLETTO 15 REGISTRATION # 3005509212
Manufacturer CityVAL DELLA TORRE, 10040
Manufacturer CountryIT
Manufacturer Postal Code10040
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameSTREAMLAB ANALYTICAL WORKCELL
Generic NameSTREAMLAB ANALYTICAL WORKCELL
Product CodeLGX
Date Received2019-07-19
Model NumberSTREAMLAB ANALYTICAL WORKCELL
Catalog Number10444806
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE DIAGNOSTICS INC.
Manufacturer Address500 GBC DRIVE PO BOX 6101 NEWARK DE 197146101 US 197146101


Patients

Patient NumberTreatmentOutcomeDate
10 2019-07-19

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