More Details

Key features of the Person lift include:
* Fixed or mobile vehicle brackets
* Left or Right side applications
* Combi option available for higher vehicles
* Sling sizes: Small, Medium and Large
* Push button handset
* Can also be used inside the home either with a mobile frame or fixed wall bracket
* EMC tested and CE marked

Kivi Combi Lift
* For high clearance vehicles as minivans, SUVs and commercial vehicles. The system consists of a lifting cylinder, a mobile bracket, an articulated arm, a sling seat and of a rocker switch or a push button handset. Its operation is the same as the K-PL100.

Method Of Use

The caregiver will position the sling seat behind the passenger's back, letting the lower edges slide under the thighs and the upper edges under the armpits. Then, he/she will fasten the four attachment points of the sling seat to attachment points on the lift arm. Upwards and downwards movement is electrically controlled by a push button handset, while the lateral movement, to enter and exit, is manually operated.

Place Of Manufacture

Italy

Price Guide

Contact supplier for prices

Models

* Kivi Person Lift
* Kivi Combi Lift - for high clearance vehicles

Installation

All vehicle modifications must be installed by an authorised agent.

The RMS requires evidence that the safety standards originally built into the vehicle have been maintained. Therefore, the modifications must be certified by an Engineering Signatory who is recognised by the RMS for this purpose. If the modifications are satisfactory, the signatory will issue an Engineering Certificate which must be presented to the RMS. The RMS maintains a list of Engineering Signatories.

Standards

Standards
Some assistive technology needs to meet Australian or other standards. Standards may relate to materials, manufacturing and installation. Products that meet Australian or international standards will have written certification. To find out if a product meets Australian Standards ask the supplier to show you the certificate. For more information about standards also see
www.ilcnsw.asn.au/home/assistive_technology/standards

TGA
Many of the items on the ILC NSW website are categorised as a Medical Device. Medical devices that are approved for use in Australia have been entered into a national database called the Australian Register of Therapeutic Goods (ARTG), which is maintained by the Therapeutic Goods Administration (TGA). You can ask the supplier for the ARTG number for the device you wish to purchase and search the ARTG for the entry. To access information on the ARTG visit www.tga.gov.au

When buying a medical device it is advisable to only choose a medical device that is recommended by a healthcare professional and has been included on the ARTG.

Please note that custom made devices are not required to undergo pre-market assessment by the TGA or to be included on the ARTG before supply. Custom made medical devices do not include medical devices that have been adapted or modified to accommodate an individual patient.