CLEARSIGHT FINGER CUFF CSCL

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-30 for CLEARSIGHT FINGER CUFF CSCL manufactured by Edwards Lifesciences Dr.

MAUDE Entry Details

Report Number2015691-2019-02819
MDR Report Key8842045
Date Received2019-07-30
Date of Report2019-07-12
Date of Event2019-07-12
Date Mfgr Received2019-07-12
Date Added to Maude2019-07-30
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 DR
Manufacturer StreetPARQUE INDUSTRIAL DE ITABO CARR. SANCHEZ KM 18.5
Manufacturer CityHAINA, SAN CRISTOBAL
Manufacturer CountryDR
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameCLEARSIGHT FINGER CUFF
Generic NameSYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE
Product CodeDXN
Date Received2019-07-30
Model NumberCSCL
Catalog NumberCSCL
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerEDWARDS LIFESCIENCES DR
Manufacturer AddressPARQUE INDUSTRIAL DE ITABO CARR. SANCHEZ KM 18.5 HAINA, SAN CRISTOBAL DR


Patients

Patient NumberTreatmentOutcomeDate
10 2019-07-30

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