RIFTON HYGIENE AND TOILETING SYSTEM Z110

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-10-01 for RIFTON HYGIENE AND TOILETING SYSTEM Z110 manufactured by Rifton Equipment.

MAUDE Entry Details

Report Number3010761454-2019-00001
MDR Report Key9139223
Date Received2019-10-01
Date of Report2019-10-01
Date of Event2019-09-04
Date Mfgr Received2019-09-05
Device Manufacturer Date2017-03-20
Date Added to Maude2019-10-01
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. TRAVIS SCOTT
Manufacturer Street103 WOODCREST DRIVE
Manufacturer CityRIFTON NY 12471
Manufacturer CountryUS
Manufacturer Postal12471
Manufacturer Phone8456587722
Manufacturer G1RIFTON EQUIPMENT
Manufacturer Street100 SPRING VALLEY ROAD
Manufacturer CityFARMINGTON PA 15437
Manufacturer CountryUS
Manufacturer Postal Code15437
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameRIFTON HYGIENE AND TOILETING SYSTEM
Generic NameTOILET CHAIR
Product CodeINN
Date Received2019-10-01
Model NumberZ110
Catalog NumberZ110
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerRIFTON EQUIPMENT
Manufacturer Address100 SPRING VALLEY ROAD FARMINGTON PA 15437 US 15437


Patients

Patient NumberTreatmentOutcomeDate
10 2019-10-01

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