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sidhil PLUS II Dynamic User Instructions

Mattress replacement system
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PLUS II
Dynamic Mattress Replacement System
User Instructions

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Summary of Contents for sidhil PLUS II Dynamic

  • Page 1 PLUS II Dynamic Mattress Replacement System User Instructions...

  • Page 3: Table Of Contents

    CONTENTS Important Notice Before operating this medical equipment, it is important to read this manual and understand the operating instructions and safety precautions. Failure to do so could result in injury and/or damage to the product. If you have any questions, please see contact information on rear cover.

  • Page 4: Introduction

    INTRODUCTION Plus II Dynamic Mattress Replacement System Thank you for choosing a Plus II Dynamic Mattress Replacement System. This user manual should be read carefully before using the mattress as it contains important information regarding safe operation and maintenance in order to provide long lasting and reliable service.

  • Page 5: Safety Precautions

    SAFETY PRECAUTIONS In General Control Unit Do not use this equipment in the The control unit is tested and CE marked presence of flammable anaesthetics. in line with Medical Device Directive (93/42/ EEC). Keep away from sources of heat and naked flames.

  • Page 6: Product Overview

    PRODUCT OVERVIEW Alternating Mattress System (see Technical Specification) The Plus II Dynamic Mattress Replacement Control Unit System is intended to provide comfort and The control unit provides the air supply to the pressure relief to patients vulnerable to mattress. pressure damage. It is designed for use on •...

  • Page 7: Installation

    INSTALLATION Any damaged or missing components should be reported to your supplier as soon as possible. System Installation Control Unit Activation The following describes the procedures for a. Position the control unit by hanging the initial system set up: hooks over the foot board or place unit on the floor under the bed with the front a.
  • Page 8 INSTALLATION To attach the handle to the control unit: 1) Depress the lever on the top of the handle. 2) Aligning the ports on the handle with those on the control box, firmly push the handle into position. 3) Release the lever, ensuring this has engaged onto the catch connected to the control box.

  • Page 9: Operation

    OPERATION Control Unit Panel A Power Button F Max Button Turns system on/off by pressing for at least two Pressing the ‘max’ button facilitates rapid seconds. inflation to the maximum pressure setting (60mmHg), the orange ‘static’ LED will B Alarm LED illuminate.

  • Page 10: Mattress Function

    OPERATION Mattress Function Establishing Pressure (supine patient) Establishing Pressure (upright position) With the patient lying supine (face upwards), use the ‘+/-’ functions to establish the best When moving the patient to a sitting or more setting for effective support and comfort. upright position, the pressure may need to be increased to provide added support and to Before changing or lowering the pressure,...

  • Page 11: Use Of Incontinence Products

    OPERATION To gain access to the sealing connectors, unzip the top cover past the CPR tag. Push together keeping both halves parallel to each other. Use of Incontinence Products Static Mode Incontinence products such as sheets or Patients should always be nursed on the pads can be used with this system.

  • Page 12: Removal & Transport Function

    OPERATION System Removal Transport Function 1. Turn off the control unit by pressing the 1. Before patient transport, switch modes power button for at least 2 seconds and from alternating to static and wait for 12 unplug the mains cable. minutes for all cells to inflate.

  • Page 13: Troubleshooting

    TROUBLESHOOTING The red alarm LED flashes, and an audible alert sounds, to indicate the control unit or mattress pressure has failed. The LED will remain illuminated until appropriate pressure is restored. The audible alarm can be silenced by pressing the alarm mute button. The system has five different alarm signals, identified by five different pressure setting illumination sequences.
  • Page 14 2. To check effective system performance, conduct a weight bottoming out test as described previously. If the above actions fail to rectify the problem please contact your local authorised service provider or Sidhil Limited.

  • Page 15: Cleaning

    CLEANING Wipe down with a disposable soft cloth Infection Control moistened with a mild detergent and diluted in Routine cleaning for infection control must warm water (40˚C), dry thoroughly before use. be carried out in accordance with your local Wipe down with a solution of Sodium infection control policy or regulatory body.

  • Page 16: Maintenance

    Failure to do so may result in the product warranty becoming void. The mattress system must be serviced once yearly, as a minimum. Sidhil also recommends that the carer performs frequent visual and operational inspections. If there are any signs of damage or the system is not performing as it should withdraw it from service until the system has been repaired and is fit for use again.

  • Page 17: Technical Specification

    TECHNICAL SPECIFICATION Control System Digital micro controller Cycle Time 12 minutes Supply Voltage 230V, 50Hz 0.2A for Control Unit Fuse Rating Mains Plug – 3AMP Control Unit – 1AMP (x1) Power Rating 12VA Standards CE marked in line with Medical Devices Directive (93/42/EEC) No.
  • Page 18 TECHNICAL SPECIFICATION Definition of Symbolys Used The following symbols may appear in this manual, on the Control Unit, or on its accessories. Some of the symbols represent standards and compliances associated with the Control Unit and its use. Caution: Consult accompanying documents Class II equipment Manufacturer Serial number...
  • Page 19 TECHNICAL SPECIFICATION TECHNICAL SPECIFICATION Declaration – electromagnetic emissions- for all ME EQUIPMENT and ME SYSTEMS Guidance and manufacture’s declaration – electromagnetic emission The Plus II is intended for use in the electromagnetic environment specified below. The customer or the user of the Plus II should ensure that it is used in such an environment. Emission test Compliance Electromagnetic...
  • Page 20 TECHNICAL SPECIFICATION Declaration – electromagnetic immunity Guidance and manufacture’s declaration – electromagnetic immunity The Plus II is intended for use in the electromagnetic environment specified below. The customer or the user of the Plus II should ensure that it is used in such an environment. Immunity test IEC 60601 Compliance Electromagnetic...
  • Page 21 TECHNICAL SPECIFICATION TECHNICAL SPECIFICATION Declaration – electromagnetic immunity – for ME EQUIPMENT and ME SYSTEMS that are not LIFE-SUPPORTING Guidance and manufacture’s declaration – electromagnetic immunity The Plus II is intended for use in the electromagnetic environment specified below. The customer or the user of the Plus II should ensure that it is used in such an environment.
  • Page 22 TECHNICAL SPECIFICATION Recommended separation distances between portable and mobile RF communications equipment and the EQUIPMENT or SYSTEM – for ME EQUIPMENT or ME SYSTEM that are not LIFE-SUPPORTING Recommended separation distances between portable and mobile RF communications equipment and the Plus II Alternating Control Unit The Plus II is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled.

  • Page 23: Warranty Information

    Sidhil Ltd guarantees this product is free from defects in material and workmanship under normal use for two (2) years from the date of purchase from Sidhil Ltd and its subsidiary companies or its authorised dealers. All implied warranties, including but not limited to those implied warranties of fitness and merchantability, are limited in the total duration of one year from date of purchase.
  • Page 24 CONTACT INFORMATION Tel: 01422 233000 Fax: 01422 233010 Email: sales@sidhil.com www.sidhil.com Sidhil Business Park, Holmfield, Halifax, HX2 9TN A member of the Siddall & Hilton Ltd. Group of Companies (93/42/EEC) Certificate No. FM14550 INSTRUC/PLUSII - 05-08-2011 - REV3...

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