OUTBACK ELITE 120CM RE-ENTRY N/A OTB59120A

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 2019-11-07 for OUTBACK ELITE 120CM RE-ENTRY N/A OTB59120A manufactured by Cordis De Mexico.

MAUDE Entry Details

Report Number9616099-2019-03338
MDR Report Key9290045
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-11-07
Date of Report2019-11-22
Date of Event2019-10-19
Date Mfgr Received2019-11-20
Device Manufacturer Date2019-05-13
Date Added to Maude2019-11-07
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 ContactKARLA CASTRO
Manufacturer Street14201 NW 60TH AVE
Manufacturer CityMIAMI LAKES FL 33014
Manufacturer CountryUS
Manufacturer Postal33014
Manufacturer Phone7863138372
Manufacturer G1CORDIS DE MEXICO
Manufacturer StreetCIRCUITO INT NTE 1820
Manufacturer CityJUAREZ 32575
Manufacturer CountryMX
Manufacturer Postal Code32575
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameOUTBACK ELITE 120CM RE-ENTRY
Generic NameCATHETER FOR CROSSING TOTAL OCCLUSIONS
Product CodePDU
Date Received2019-11-07
Model NumberN/A
Catalog NumberOTB59120A
Lot Number17860363
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCORDIS DE MEXICO
Manufacturer AddressCIRCUITO INT NTE 1820 JUAREZ 32575 MX 32575


Patients

Patient NumberTreatmentOutcomeDate
10 2019-11-07

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