SWAN-GANZ BIPOLAR PACING CATHETER D97120F5

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-02 for SWAN-GANZ BIPOLAR PACING CATHETER D97120F5 manufactured by Edwards Lifesciences Pr.

MAUDE Entry Details

Report Number2015691-2020-10781
MDR Report Key9774742
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-02
Date of Report2020-02-13
Date of Event2020-02-10
Date Mfgr Received2020-03-12
Device Manufacturer Date2019-02-28
Date Added to Maude2020-03-02
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 ContactMRS LYNN THOMAS
Manufacturer Street1 EDWARDS WAY
Manufacturer CityIRVINE CA 92614
Manufacturer CountryUS
Manufacturer Postal92614
Manufacturer Phone9497564386
Manufacturer G1EDWARDS LIFESCIENCES PR
Manufacturer StreetSTATE RD INDUS PK 402 KM 1.4
Manufacturer CityANASCO
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSWAN-GANZ BIPOLAR PACING CATHETER
Generic NameCATHETER, FLOW DIRECTED
Product CodeDYG
Date Received2020-03-02
Returned To Mfg2020-03-06
Model NumberD97120F5
Catalog NumberD97120F5
Lot Number61913157
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerEDWARDS LIFESCIENCES PR
Manufacturer AddressSTATE RD INDUS PK 402 KM 1.4 ANASCO PR


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-02

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.