CENTRALINK DATA MANAGEMENT SYSTEM 11314337

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 2020-01-10 for CENTRALINK DATA MANAGEMENT SYSTEM 11314337 manufactured by Siemens Healthcare Diagnostics Inc..

MAUDE Entry Details

Report Number2432235-2020-00035
MDR Report Key9578646
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2020-01-10
Date of Report2020-03-09
Date of Event2019-12-02
Date Mfgr Received2020-02-10
Date Added to Maude2020-01-10
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 ContactCHRISTINA LAM
Manufacturer Street511 BENEDICT AVE
Manufacturer CityTARRYTOWN, NY NY 10591
Manufacturer CountryUS
Manufacturer Postal10591
Manufacturer Phone9145243504
Manufacturer G1SIEMENS HEALTHCARE DIAGNOSTICS MANUFACTURING LTD.
Manufacturer StreetCHAPEL LANE, SWORDS, CO. REGISTRATION NUMBER: 8020888
Manufacturer CityDUBLIN,
Manufacturer CountryEI
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCENTRALINK DATA MANAGEMENT SYSTEM
Generic NameCENTRALINK DATA MANAGEMENT SYSTEM
Product CodeJQP
Date Received2020-01-10
Model NumberCENTRALINK DATA MANAGEMENT SYSTEM
Catalog Number11314337
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE DIAGNOSTICS INC.
Manufacturer Address511 BENEDICT AVE TARRYTOWN NY 10591 US 10591


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-10

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