EPIQ 7C - 795201

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-09 for EPIQ 7C - 795201 manufactured by Philips Ultrasound, Inc.

MAUDE Entry Details

Report Number3019216-2019-00041
MDR Report Key8773992
Date Received2019-07-09
Date of Report2019-06-24
Date Mfgr Received2019-06-24
Device Manufacturer Date2018-02-27
Date Added to Maude2019-07-09
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationBIOMEDICAL ENGINEER
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. PAUL CORRIGAN
Manufacturer Street22100 BOTHELL EVERETT HIGHWAY
Manufacturer CityBOTHELL WA 98021
Manufacturer CountryUS
Manufacturer Postal98021
Manufacturer Phone4254877000
Manufacturer G1PHILIPS MEDICAL SYSTEMS
Manufacturer Street3000 MINUTEMAN ROAD
Manufacturer CityANDOVER MA 01810
Manufacturer CountryUS
Manufacturer Postal Code01810
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameEPIQ 7C - 795201
Generic NameSYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC22
Product CodeIYN
Date Received2019-07-09
Model NumberEPIQ 7C - 795201
Catalog NumberEPIQ 7C - 795201
Lot NumberUS218B1150
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerPHILIPS ULTRASOUND, INC
Manufacturer Address22100 BOTHELL EVERETT HIGHWAY BOTHELL WA 98021 US 98021


Patients

Patient NumberTreatmentOutcomeDate
10 2019-07-09

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