SHOCKWAVE S4 PERIPHERAL IVL CATHETER 61163-3540 S4IVL3540

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2019-06-13 for SHOCKWAVE S4 PERIPHERAL IVL CATHETER 61163-3540 S4IVL3540 manufactured by Shockwave Medical, Inc..

MAUDE Entry Details

Report Number3010940016-2019-00002
MDR Report Key8697738
Report SourceCOMPANY REPRESENTATIVE
Date Received2019-06-13
Date of Report2019-06-13
Date of Event2019-05-16
Date Mfgr Received2019-05-16
Device Manufacturer Date2019-01-08
Date Added to Maude2019-06-13
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 ContactMR. RYAN KIRTLAND
Manufacturer Street48501 WARM SPRINGS BLVD. SUITE 108
Manufacturer CityFREMONT CA 94539
Manufacturer CountryUS
Manufacturer Postal94539
Manufacturer Phone5106249076
Manufacturer G1SHOCKWAVE MEDICAL, INC
Manufacturer Street48501 WARM SPRINGS BLVD. SUITE 108
Manufacturer CityFREMONT CA 94539
Manufacturer CountryUS
Manufacturer Postal Code94539
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSHOCKWAVE S4 PERIPHERAL IVL CATHETER
Generic NameBALLOON CATHETER
Product CodePPN
Date Received2019-06-13
Model Number61163-3540
Catalog NumberS4IVL3540
Lot NumberP190108C
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSHOCKWAVE MEDICAL, INC.
Manufacturer Address48501 WARM SPRINGS BLVD. SUITE 108 FREMONT CA 94539 US 94539


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Required No Informationntervention 2019-06-13

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