452201100661

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-09-16 for 452201100661 manufactured by Invivo Corporation.

MAUDE Entry Details

Report Number1051786-2019-00036
MDR Report Key9069836
Date Received2019-09-16
Date of Report2019-08-19
Date Mfgr Received2019-08-19
Device Manufacturer Date2004-03-02
Date Added to Maude2019-09-16
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. ROBERT CORNING
Manufacturer Street12151 RESEARCH PARKWAY SUITE 200
Manufacturer CityORLANDO FL 32826
Manufacturer CountryUS
Manufacturer Postal32826
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

Generic NameCARDIOVASCULAR MONITOR
Product CodeMWI
Date Received2019-09-16
Model Number452201100661
Lot NumberN/A
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerINVIVO CORPORATION
Manufacturer Address12151 RESEARCH PARKWAY SUITE 200 ORLANDO FL 32826 US 32826


Patients

Patient NumberTreatmentOutcomeDate
10 2019-09-16

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