VAPR3 FOOTSWITCH *EA 225023

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,other report with the FDA on 2020-03-18 for VAPR3 FOOTSWITCH *EA 225023 manufactured by Depuy Mitek Llc Us.

MAUDE Entry Details

Report Number1221934-2020-00898
MDR Report Key9849445
Report SourceCOMPANY REPRESENTATIVE,OTHER
Date Received2020-03-18
Date of Report2020-03-04
Date of Event2020-03-04
Date Mfgr Received2020-03-04
Date Added to Maude2020-03-18
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 ContactKARA DITTY-BOVARD
Manufacturer Street325 PARAMOUNT DRIVE
Manufacturer CityRAYNHAM MA 02767
Manufacturer CountryUS
Manufacturer Postal02767
Manufacturer Phone6103142063
Manufacturer G1DEPUY MITEK
Manufacturer Street325 PARAMOUNT DRIVE
Manufacturer CityRAYNHAM MA 02767
Manufacturer CountryUS
Manufacturer Postal Code02767
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameVAPR3 FOOTSWITCH *EA
Generic NameFOOT-SWITCH, ELECTRICAL
Product CodeHRX
Date Received2020-03-18
Model Number225023
Catalog Number225023
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device Availability*
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDEPUY MITEK LLC US
Manufacturer Address325 PARAMOUNT DRIVE RAYNHAM MA 02767 US 02767


Patients

Patient NumberTreatmentOutcomeDate
10 2020-03-18

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