SOUNDSTAR ECO 8F ULTRASOUND CATHETER 10439011

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 2020-03-17 for SOUNDSTAR ECO 8F ULTRASOUND CATHETER 10439011 manufactured by Biosense Webster Inc..

MAUDE Entry Details

Report Number2029046-2020-00432
MDR Report Key9844932
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-03-17
Date of Report2020-02-27
Date of Event2020-02-27
Date Mfgr Received2020-02-27
Date Added to Maude2020-03-17
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. GABRIEL ALFAGEME
Manufacturer Street31 TECHNOLOGY DRIVE
Manufacturer CityIRVINE CA 92618
Manufacturer CountryUS
Manufacturer Postal92618
Manufacturer Phone949789-868
Manufacturer G1BIOSENSE WEBSTER INC (IRWINDALE)
Manufacturer Street15715 ARROW HIGHWAY
Manufacturer CityIRWINDALE CA 91706
Manufacturer CountryUS
Manufacturer Postal Code91706
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSOUNDSTAR ECO 8F ULTRASOUND CATHETER
Generic NameCATHETER, ULTRASOUND, INTRAVASCULAR
Product CodeOBJ
Date Received2020-03-17
Model Number10439011
Catalog Number10439011
Lot NumberE8220801
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerBIOSENSE WEBSTER INC.
Manufacturer Address33 TECHNOLOGY DRIVE IRVINE CA 92618 US 92618


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization; 2. Life Threatening; 3. Required No Informationntervention 2020-03-17

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