JACKSON ANG 4MM CUP FCPS 28CM 505100

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-07-12 for JACKSON ANG 4MM CUP FCPS 28CM 505100 manufactured by Teleflex Medical.

MAUDE Entry Details

Report Number3011137372-2019-00234
MDR Report Key8786292
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-07-12
Date of Report2019-06-19
Date of Event2019-06-17
Date Mfgr Received2019-08-01
Date Added to Maude2019-07-12
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 ContactJASMINE BROWN
Manufacturer Street3015 CARRINGTON MILL BLVD
Manufacturer CityMORRISVILLE NC 27560
Manufacturer CountryUS
Manufacturer Postal27560
Manufacturer Phone9193614124
Manufacturer G1TELEFLEX MEDICAL
Manufacturer Street3015 CARRINGTON MILL BLVD
Manufacturer CityMORRISVILLE NC 27560
Manufacturer CountryUS
Manufacturer Postal Code27560
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameJACKSON ANG 4MM CUP FCPS 28CM
Generic NameJACKSON STR 4MM CUP FCPS 28CM
Product CodeGEN
Date Received2019-07-12
Returned To Mfg2019-07-17
Catalog Number505100
Lot NumberNA
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerTELEFLEX MEDICAL
Manufacturer AddressRESEARCH TRIANGLE PARK NC


Patients

Patient NumberTreatmentOutcomeDate
10 2019-07-12

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