SITE~RITE 8 ULTRASOUND SYSTEM CONSOLE WITH CONNECTOR 9770600

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-03-05 for SITE~RITE 8 ULTRASOUND SYSTEM CONSOLE WITH CONNECTOR 9770600 manufactured by Bard Access Systems.

MAUDE Entry Details

Report Number3006260740-2020-00775
MDR Report Key9794334
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-03-05
Date of Report2020-03-05
Date Mfgr Received2020-02-13
Date Added to Maude2020-03-05
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 ContactSHELLY GILBERT
Manufacturer Street605 N. 5600 W.
Manufacturer CitySALT LAKE CITY UT 84116
Manufacturer CountryUS
Manufacturer Postal84116
Manufacturer Phone8015225640
Manufacturer G1DYMAX CORP.
Manufacturer Street141 ZEHNER SCHOOL ROAD
Manufacturer CityZELIENOPLE PA 16063
Manufacturer CountryUS
Manufacturer Postal Code16063
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSITE~RITE 8 ULTRASOUND SYSTEM CONSOLE WITH CONNECTOR
Generic NameSYSTEM, IMAGING, PULSED ECHO, ULTRASONIC
Product CodeIYO
Date Received2020-03-05
Returned To Mfg2020-02-28
Model Number9770600
Catalog Number9770600
Lot NumberN/A
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerBARD ACCESS SYSTEMS
Manufacturer Address605 N. 5600 W. SALT LAKE CITY UT 84116 US 84116


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-05

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