TRA

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a consumer report with the FDA on 2020-02-03 for TRA manufactured by Tisport, Llc.

MAUDE Entry Details

Report Number3032618-2020-00002
MDR Report Key9663147
Report SourceCONSUMER
Date Received2020-02-03
Date of Report2020-02-03
Date of Event2020-01-06
Date Mfgr Received2020-01-06
Device Manufacturer Date2018-01-25
Date Added to Maude2020-02-03
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 ContactFRED ORTMANN
Manufacturer Street2701 W COURT ST
Manufacturer CityPASCO WA 99301
Manufacturer CountryUS
Manufacturer Postal99301
Manufacturer Phone5095866117
Single Use3
Remedial ActionRL
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTRA
Generic NameWHEELCHAIR
Product CodeIOR
Date Received2020-02-03
Model NumberTRA
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerTISPORT, LLC
Manufacturer Address2701 W COURT ST PASCO WA 99301 US 99301


Patients

Patient NumberTreatmentOutcomeDate
101. Hospitalization 2020-02-03

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