Getinge ARJOHUNTLEIGH AURA Instructions For Use Manual
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Getinge ARJOHUNTLEIGH AURA Instructions For Use Manual

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AURA
Instructions for Use
0086
...with people in mind

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Summary of Contents for Getinge ARJOHUNTLEIGH AURA

  • Page 1 AURA Instructions for Use 0086 ...with people in mind...

  • Page 3: Table Of Contents

    Contents General Safety ............iii Introduction .
  • Page 4 (ii)

  • Page 5: General Safety

    GENERAL SAFETY Before you connect the system pump to a mains socket, read carefully all the installation instructions contained within this manual. The system has been designed to comply with regulatory safety standards including: • EN60601-1:1990/A13:1996 and IEC 60601-1:1988/A2:1995 • UL60601-1, UL2601-1 and CAN/CSA C22.2 No. 601.1-M90 •...
  • Page 6 Electromagnetic Compatibility (EMC) This product complies with the requirements of applicable EMC Standards. Medical electrical equipment needs special precautions regarding EMC and needs to be installed in accordance with the following instructions: • The use of accessories not specified by the manufacturer may result in increased emissions by, or decreased immunity of, the equipment, affecting its performance.

  • Page 7: Introduction

    1. Introduction ® About this Manual Aura This manual is your introduction to the system. You must read and fully understand this manual before using the system. Use this manual to initially set up the system, and keep it as a reference for day-to-day routines and as a guide to maintenance.
  • Page 8 Aura Seat Cushion Cover Straps Cells...

  • Page 9: Clinical Applications

    2. Clinical Applications Indications The Aura systems are indicated for the prevention and/ or management of all categories of pressure ulcer, when combined with an individualised, comprehensive pressure ulcer protocol: for example, repositioning, nutritional support, skin care. Selection should be based upon a holistic assessment of the patient’s individual care needs.

  • Page 10: Installation

    3. Installation The system is simple to set up and the following guidelines may assist you. Preparing the Aura 1. Remove the contents of the packaging. You should Cushion and Pump have the following items: Aura • pump with integral mains power cord and hanging bracket.
  • Page 11 7. If the chair is of the open sided construction, then fix the cushion as shown below. 8. If the chair is of the closed side type with a Aura removable seat cushion, fix the cushion as shown below. 9. If the chair is of the closed side type with a non- removable seat cushion, then security will rely on Aura the anti-slip pads on the base of the...

  • Page 12: Controls, Indicators And Alarms

    4. Controls, Indicators and Alarms Controls Run/Standby Switch This is situated on the side panel of the pump and is used to activate the unit and reset the alarm. Mains isolation should be performed by switching the pump to standby ( ) and then removing the mains plug from the socket.

  • Page 13: Operation

    5. Operation These instructions cover day-to-day operation of the system. Other operations, such as maintenance and repair, should only be carried out by suitably qualified personnel.  Refer to Section 4, Page 6 “Controls, Indicators and Alarms” for a comprehensive description of the controls and indicators on the pump. ...

  • Page 14: Deflating The Seat Cushion

    Deflating the To deflate and store the seat cushion, do the following: Seat Cushion 1. Switch off the pump, and disconnect the pump from the mains power supply. 2. Remove the tubeset from the pump. 3. Deflate the seat cushion. ...

  • Page 15: Decontamination

    6. Decontamination The following processes are recommended, but should be adapted to comply with the local or national guidelines (Decontamination of Medical Devices) which may apply within the Healthcare Facility or the country of use. If you are uncertain, you should seek advice from your local Infection Control Specialist.
  • Page 16 DO NOT WRING/MANGLE, AUTOCLAVE OR USE PHENOLIC BASED SOLUTIONS. Thermal Disinfection For information for the seat top cover, including laundering guidelines, refer to “Cleaning Symbols” on page 14. Re-use with multiple Professional hygiene maintenance is required before re-use of the system with a different patient. patients...

  • Page 17: Troubleshooting Guide

    7. Troubleshooting Guide Problem Possible Cause Action Seat cushion not inflating. 1. Tubes kinked. Check 2. Pump not switched on. Check 3. No pump output. Check 4. Punctured cell or leakage Check. See Pump not from T-connector operating below 5. Tubes not correctly fitted. Check Consistent Low Pressure 1.

  • Page 18: Technical Description

    8. Technical Description PUMP Model: Aura Part Numbers: ALS01 ALS03 Supply Voltage: 230 V 120 V Supply Frequency: 50 Hz 60 Hz Power Input: 14 VA 14 VA Size: 248 x 160 x 116 mm (9.8 x 6.3 x 4.6 in.) Weight: 2.75 kg (6 lb) Case Material:...

  • Page 19: Seat

    PUMP SYMBOLS The operator must read this document Do not dispose of in (Instructions for Use) Standby domestic refuse before use. Note: This symbol is blue on the product label. With respect to electric shock, fire and mechanical hazards only in accordance with CAN/ Type BF CSA-C22.2 No.

  • Page 20: Cover Specification

    COVER SPECIFICATION Standard Cover Feature ® (Dartex Removable Cover Moisture Vapour Permeable Air Permeable Low Friction Water Resistant / Repellent Infection Control Material coating is bacteriostatic, fungistatic, antimicrobial Fire Retardant BS 7175: 0,1 & 5 2-Way Stretch MAX 95°C (203°F) for 15 mins Washing Conditions Tumble Dry up to 130°C (266°F) or Air Dry Drying Conditions...
  • Page 21 Guidance and manufacturer’s declaration - electromagnetic emissions The pump is intended for use in the electromagnetic environment specified below. The customer or the user of the pump should assure that it is used in such an environment. Emissions Test Compliance Electromagnetic environment - guidance RF emissions Group 1...
  • Page 22 Guidance and manufacturer’s declaration - electromagnetic immunity The pump is intended for use in the electromagnetic environment specified below. The customer or the user of the Nimbus pump should assure that it is used in such an environment. Immunity Test IEC 60601 Test Compliance Electromagnetic environment - guidance...
  • Page 23 AUSTRALIA FAR EAST PORTUGAL ArjoHuntleigh Pty Ltd ARJO Far East Limited ArjoHuntleigh em Portugal: 78, Forsyth street Unit 3A, 4/F., Block B Hoi Luen MAQUET Portugal, Lda. O’Connor Industrial Centre (Distribudor Exclusivo) AU-6163 Western Australia 55 Hoi Yuen Road, Rua Poeta Bocage n.º 2 - 2G Tel: +61 89337 4111 Kwun Tong, Kowloon 1600-233 Lisboa, Portugal...
  • Page 24 GETINGE GROUP is a leading global provider of products and systems that contribute to quality enhancement and cost efficiency within healthcare and life sciences. We operate under the three brands of ArjoHuntleigh, GETINGE and MAQUET. ArjoHuntleigh focuses on patient mobility and wound management solutions.

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