AEROMINI?.STENT, TRACHEOBRONCHIAL AERO615

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 2019-12-20 for AEROMINI?.STENT, TRACHEOBRONCHIAL AERO615 manufactured by Merit Medical Systems, Inc..

MAUDE Entry Details

Report Number3010665433-2019-00086
MDR Report Key9501097
Report SourceCOMPANY REPRESENTATIVE,HEALTH
Date Received2019-12-20
Date of Report2019-12-04
Date of Event2019-12-04
Date Mfgr Received2019-12-04
Date Added to Maude2019-12-20
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 ContactMR DAVID LOCKRIDGE
Manufacturer Street1600 MERIT PARKWAY
Manufacturer CitySOUTH JORDAN UT 84095
Manufacturer CountryUS
Manufacturer Postal84095
Manufacturer Phone8012084551
Manufacturer G1MERIT MEDICAL SYSTEMS, INC.
Manufacturer Street14646 KIRBY DRIVE
Manufacturer CityHOUSTON TX 77047
Manufacturer CountryUS
Manufacturer Postal Code77047
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAEROMINI?.STENT, TRACHEOBRONCHIAL
Generic NameTRACHEOBRONCHIAL STENT
Product CodeJCT
Date Received2019-12-20
Catalog NumberAERO615
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerMERIT MEDICAL SYSTEMS, INC.
Manufacturer Address14646 KIRBY DRIVE HOUSTON TX 77047 US 77047


Patients

Patient NumberTreatmentOutcomeDate
10 2019-12-20

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