Huntleigh LP110 - Table of Contents

3
Installation Guide
Contents
1. Contraindications ................................................................................4
2. Introduction .........................................................................................4
3. Detail .....................................................................................................5
3.1 Dimensions ............................................................................................. 5
3.2 Clearances .............................................................................................. 5
3.3 Rear Connections .................................................................................. 6
3.3.1 Equi-potential Earth Connection............................................................................. 6
3.3.2 Trigger Output Connection .....................................................................................7
3.4 Gantry Mounting .................................................................................... 7
3.5 Mobile Cart /Table Pedestal Mounting ................................................. 8
3.6 Attaching to a Mobile Cart/Table Pedestal .......................................... 9
3.6.1 Mobile Cart ............................................................................................................. 9
3.6.2 Table Pedestal ........................................................................................................ 10
4. Service ..................................................................................................11
Manufactured in the UK for CANON Medical Systems by Huntleigh Healthcare Ltd.
As part of the ongoing development programme the company reserves the right to modify
specifi cations and materials of the Lifepulse range without notice.
Lifepulse, Huntleigh and ‘H’ logo are registered trademarks of Huntleigh Technology Ltd.
2010.
© Huntleigh Healthcare Ltd. 2010
The LP110/LP110-S complies with the essential requirements of the Medical
Device Directive (93/42/EEC) - Medical Device Regulation (EU/2017/745)