KENDALL 7365 50007365

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-09-18 for KENDALL 7365 50007365 manufactured by Covidien.

MAUDE Entry Details

Report Number9081146
MDR Report Key9081146
Date Received2019-09-18
Date of Report2019-08-28
Date of Event2019-08-15
Report Date2019-08-28
Date Reported to FDA2019-08-28
Date Reported to Mfgr2019-09-18
Date Added to Maude2019-09-18
Event Key0
Report Source CodeUser Facility report
Manufacturer LinkN
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
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameKENDALL
Generic NameELECTRODE, ELECTROCARDIOGRAPH
Product CodeDRX
Date Received2019-09-18
Model Number7365
Catalog Number50007365
Lot Number906331
Device Availability*
Device Eval'ed by Mfgr*
Device Sequence No1
Device Event Key0
ManufacturerCOVIDIEN
Manufacturer Address1313 WEST GRANT BLVD. WABASHA MN 55981 US 55981


Patients

Patient NumberTreatmentOutcomeDate
10 2019-09-18

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