ENSITE VELOCITY? SYSTEM VELOCITY AMPLIFIER 100014514

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 2019-11-27 for ENSITE VELOCITY? SYSTEM VELOCITY AMPLIFIER 100014514 manufactured by St. Jude Medical, Inc.

MAUDE Entry Details

Report Number2184149-2019-00236
MDR Report Key9382948
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-11-27
Date of Report2019-11-27
Date of Event2019-11-19
Date Mfgr Received2019-11-19
Date Added to Maude2019-11-27
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 ContactSTEPHANIE O' SULLIVAN
Manufacturer Street5050 NATHAN LANE NORTH
Manufacturer CityPLYMOUTH MN 55442
Manufacturer CountryUS
Manufacturer Postal55442
Manufacturer Phone6517565400
Manufacturer G1ST. JUDE MEDICAL, INC. (AF-ST. PAUL)
Manufacturer StreetONE ST. JUDE MEDICAL DRIVE
Manufacturer CityST. PAUL MN 55117
Manufacturer CountryUS
Manufacturer Postal Code55117
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameENSITE VELOCITY? SYSTEM VELOCITY AMPLIFIER
Generic NameCOMPUTER, DIAGNOSTIC, PROGRAMMABLE
Product CodeDQK
Date Received2019-11-27
Model Number100014514
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerST. JUDE MEDICAL, INC
Manufacturer AddressONE ST. JUDE MEDICAL DRIVE ST. PAUL MN 55117 US 55117


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-11-27

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.