SMITHS MEDICAL CENTRAL VENOUS CATHETERSDELTEC LOGICATH CONVENTIONAL MXA231X20X16V

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,user facility report with the FDA on 2019-09-13 for SMITHS MEDICAL CENTRAL VENOUS CATHETERSDELTEC LOGICATH CONVENTIONAL MXA231X20X16V manufactured by Smiths Medical Asd, Inc..

MAUDE Entry Details

Report Number3012307300-2019-04907
MDR Report Key9037954
Report SourceFOREIGN,USER FACILITY
Date Received2019-09-13
Date of Report2019-10-08
Date of Event2019-05-01
Date Mfgr Received2019-09-19
Device Manufacturer Date2016-12-21
Date Added to Maude2019-09-13
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 ContactDAVE HALVERSON
Manufacturer Street6000 NATHAN LANE NORTH
Manufacturer CityMINNEAPOLIS MN 55442
Manufacturer CountryUS
Manufacturer Postal55442
Manufacturer Phone7633833310
Manufacturer G1SMITHS MEDICAL CZECH REPUBLIC A.S.
Manufacturer StreetOLOMOUCK? 306
Manufacturer CityHRANICE, 753 01
Manufacturer CountryEZ
Manufacturer Postal Code753 01
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSMITHS MEDICAL CENTRAL VENOUS CATHETERSDELTEC LOGICATH CONVENTIONAL
Generic NameCENTRAL VENOUS CATHETER DRESSING CHANGE KIT
Product CodePEZ
Date Received2019-09-13
Catalog NumberMXA231X20X16V
Lot Number3337605C
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSMITHS MEDICAL ASD, INC.
Manufacturer Address6000 NATHAN LANE NORTH MINNEAPOLIS MN 55442 US 55442


Patients

Patient NumberTreatmentOutcomeDate
10 2019-09-13

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