ATELLICA CH VANCOMYCIN (VANC) 11097511

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 2019-11-22 for ATELLICA CH VANCOMYCIN (VANC) 11097511 manufactured by Siemens Healthcare Diagnostics Inc..

MAUDE Entry Details

Report Number2432235-2019-00434
MDR Report Key9365627
Report SourceHEALTH PROFESSIONAL,USER FACI
Date Received2019-11-22
Date of Report2019-11-22
Date of Event2019-10-25
Date Mfgr Received2019-10-30
Date Added to Maude2019-11-22
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. MARDOCHEE TIMOLIEN
Manufacturer Street511 BENEDICT AVENUE
Manufacturer CityTARRYTOWN NY 10591
Manufacturer CountryUS
Manufacturer Postal10591
Manufacturer Phone9145242503
Manufacturer G1SIEMENS HEALTHCARE DIAGNOSTICS INC.
Manufacturer Street500 GBC DRIVE, PO BOX 6101 REGISTRATION # 2517506
Manufacturer CityDE 197146101
Manufacturer CountryUS
Manufacturer Postal Code197146101
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameATELLICA CH VANCOMYCIN (VANC)
Generic NameATELLICA CH VANCOMYCIN (VANC)
Product CodeLEH
Date Received2019-11-22
Model NumberATELLICA CH VANCOMYCIN (VANC)
Catalog Number11097511
Lot Number190146
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerSIEMENS HEALTHCARE DIAGNOSTICS INC.
Manufacturer Address511 BENEDICT AVENUE TARRYTOWN NY 10591 US 10591


Patients

Patient NumberTreatmentOutcomeDate
10 2019-11-22

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