ELECTRODE LARGE PUPPYDOG PEDIATRIC 31424785

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 2019-06-14 for ELECTRODE LARGE PUPPYDOG PEDIATRIC 31424785 manufactured by Covidien.

MAUDE Entry Details

Report Number9681860-2019-00504
MDR Report Key8700156
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-06-14
Date of Report2019-06-14
Date Mfgr Received2019-06-10
Date Added to Maude2019-06-14
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 ContactJILL SARAIVA
Manufacturer Street15 HAMPSHIRE STREET
Manufacturer CityMANSFIELD MA 02048
Manufacturer CountryUS
Manufacturer Postal02048
Manufacturer Phone5084524970
Manufacturer G1COVIDIEN
Manufacturer Street215 HEBERT ST
Manufacturer CityGANANOQUE K7G 2Y7
Manufacturer CountryCA
Manufacturer Postal CodeK7G 2Y7
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameELECTRODE LARGE PUPPYDOG PEDIATRIC
Generic NameELECTRODE, ELECTROCARDIOGRAPH
Product CodeDRX
Date Received2019-06-14
Model Number31424785
Catalog Number31424785
Lot Number901826X
Device AvailabilityN
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN
Manufacturer Address215 HEBERT ST GANANOQUE K7G 2Y7 CA K7G 2Y7


Patients

Patient NumberTreatmentOutcomeDate
10 2019-06-14

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