INJECTION NEEDLE CATHETER 60817 991092774

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-06-05 for INJECTION NEEDLE CATHETER 60817 991092774 manufactured by Avanos Medical Inc..

MAUDE Entry Details

Report Number8030647-2019-00052
MDR Report Key8670947
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-06-05
Date of Report2019-07-18
Date of Event2019-04-29
Date Mfgr Received2019-07-01
Device Manufacturer Date2018-01-17
Date Added to Maude2019-06-05
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 ContactMS. LISA CLARK
Manufacturer Street5405 WINDWARD PARKWAY
Manufacturer CityALPHARETTA GA 30004
Manufacturer CountryUS
Manufacturer Postal30004
Manufacturer Phone4704485444
Manufacturer G1AVENT S DE RL DE CV
Manufacturer StreetCARRETERA INTERNACIONAL SALIDA NORTE NO. 1053
Manufacturer CityMAGDALENA, CP
Manufacturer CountryUS
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameINJECTION NEEDLE CATHETER
Generic NameDH ENDOSCOPY INJECTION NEEDLE CATHETERS
Product CodeKDH
Date Received2019-06-05
Returned To Mfg2019-05-22
Model Number60817
Catalog Number991092774
Lot NumberM18011E112
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerAVANOS MEDICAL INC.
Manufacturer Address5405 WINDWARD PARKWAY ALPHARETTA GA 30004 US 30004


Patients

Patient NumberTreatmentOutcomeDate
10 2019-06-05

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