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Talley PULSAIR CHOICE User Manualline

Pressure area care mattresses and cushions
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...reducing avoidable harms
User Guidelines for Pressure Area
Care Mattresses and Cushions
QUATTRO
ACUTE Systems
®
QUATTRO
PLUS Systems
®
QUATTRO
OVERLAY Systems
®
PULSAIR
CHOICE Systems
®
POLYFLOAT SUPREMA
™
POLYFLOAT DORMIRA
™
B.A.S.E.
Seating Systems
®

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Summary of Contents for Talley PULSAIR CHOICE

  • Page 1 ...reducing avoidable harms User Guidelines for Pressure Area Care Mattresses and Cushions QUATTRO ACUTE Systems ® QUATTRO PLUS Systems ® QUATTRO OVERLAY Systems ® PULSAIR CHOICE Systems ® POLYFLOAT SUPREMA ™ POLYFLOAT DORMIRA ™ B.A.S.E. Seating Systems ®...

  • Page 2: Explanation Of Labels Symbols And Statements

    Explanation of Label Symbols and Statements Protect from heat and Caution radioactive sources Refer to instructions of use / Temperature limitation booklet Humidity limitation Medical Devices Directive 93/42/EEC Atmospheric pressure limitation North America ETL listed Suitable for connection to type BF applied parts Class II Equipment (Double Insulated)

  • Page 3: Table Of Contents

    SPECIFICATIONS EMI/EMC STATEMENT AND MANUFACTURER’S DECLARATION Introduction Thank you for choosing to use a Talley pressure area care product, effective for the prevention and management of pressure ulcers. The range of alternating air pressure products is as follows:- ACUTE: mattress replacement system for patients at very high risk of pressure l QUATTRO ®...

  • Page 4: Cautions And Warnings Information

    linen.
  • Page 5 l Intended for home healthcare use and professional healthcare facility environments where operators with medical training are continually available when patients are present. l The device is intended to be hung over the beds footboard. l Wireless equipment such as mobile phones should be kept at least 10 feet or 3.3 meters away from the equipment.

  • Page 6: Alternating Air Pressure Mattresses & Cushions Installation And User Guidelines

    Alternating Air Pressure Mattresses & Cushions Installation and User Guidelines INSTALLING MATTRESSES If using a mattress replacement system, which is intended to completely replace the bed mattress, remove any existing mattress from the bed frame. If using a mattress overlay system, ensure bed frame to be used has an existing mattress in place.
  • Page 7 Note: It is important that during the INITIALISING phase the mattress connector is not disconnected from the power unit. If this is done, the power unit must be switched off, MUTE button pressed when the sounder is heard, the mattress connector re-engaged, and the power unit restarted.
  • Page 8 correctly clicked into place, otherwise a leak may Fig. 4 occur. Attach the power lead, plug into the mains outlet and switch the power on at the side of power unit adjacent to the power lead entry. Once inflated (approx. 5 minutes) increase the comfort control setting to SEATED using the UP arrow button.
  • Page 9 and therapy is provided. The automatic default comfort setting is MEDIUM (with the exception of the QUATTRO ACUTE PAEDIATRIC mattress, which defaults to SOFT). However, if the ® patient prefers a firmer or softer mattress, increase or decrease the comfort control setting accordingly using the UP and DOWN arrow buttons (SOFT/MEDIUM/FIRM).
  • Page 10 CPR FACILITY (Fig. 5) Fig. 5 The CPR device is situated at the head end on the right hand side of the mattress (viewed from foot end), as indicated by arrows on the mattress tag. For rapid deflation rotate the dial of the CPR device anti-clockwise to ‘click’...

  • Page 11: Care And Maintenance

    The individual cells can also be wiped clean with a mild antiseptic solution*. l All cells are replaceable and can be obtained easily from Talley. l Do not immerse the PULSAIR CHOICE mattresses/cushion in water.
  • Page 12 Talley personnel to bag the equipment if the mattress has been in a known or suspected infectious environment. TRANSPORT AND STORAGE Handle with care.

  • Page 13: Fault Finding

    All systems have a fault log that records the last 5 faults via the DATA display mode. If problems reoccur contact Talley. AC FAIL fault – indicates a mains power failure, a sounder will be heard if power is interrupted, e.g.
  • Page 14 PUMP OR TRIAC fault - indicates a pump control failure or an open pump coil fault. Should this occur, contact Talley. UNCALIBRATED - contact Talley for recalibration. If you have any queries relating to this system please contact Talley or your local authorised dealer. ROTOR...

  • Page 15: Installation And User Guidelines

    Static Foam Mattresses Installation and User Guidelines MATTRESSES Ensure the bed frame to be used has no existing mattress components, and is free from items which could cause damage to the POLYFLOAT SUPREMA™ / POLYFLOAT DORMIRA™ mattress. It should be noted that this mattress is intended to completely replace the existing mattresses.
  • Page 16 POLYFLOAT SUPREMA™ mattress has a 2 way turning cycle. Please refer to instructions printed on cover. SYSTEM DESIGN LIFE: 3 years HANDLING AND STORAGE Handle with care. Please report instances of damage or impact to Talley Service Department. The mattress should be stored flat. Temperature: Operational: 10 C to 40 Storage: 10...

  • Page 17: Specifications

    5 metres / 16.5’ For the USA:- only a hospital grade attachment plug with a 15A NEMAP 5-15 configuration and 18AWG hospital grade flexible cord is to be used, as supplied by Talley. Electricity Supply: 230V ~ 50Hz (CE marked)
  • Page 18 PLUS / PULSAIR QUATTRO CHOICE MATTRESS REPLACEMENT: ® ® 1950mm x 880mm x 180mm QUATTRO OVERLAY/ PULSAIR CHOICE MATTRESS OVERLAY: ® ® 1930mm x 850mm x 130mm Weight: QUATTRO ACUTE: 12.5kg (PAEDIATRIC version: 6.6kg) n QUATTRO ® ® PLUS: 10.5kg n QUATTRO OVERLAY: 6.8 kg n PULSAIR CHOICE: ®...

  • Page 19: Emi/Emc Statement And Manufacturer's Declaration

    EMI/EMC Statement and Manufacturer’s Declaration This equipment has been tested and found to comply with the limits of EN 60601-1-2. These limits are designed to provide reasonable protection against harmful interference in both a medical and residential environment. This equipment generates, uses and can radiate radio frequency energy and, if not used in accordance with manufacturer’s instructions, may cause harmful interference to radio communications.
  • Page 20 This medical device is compliant with: IEC 60601.1 3rd edition Medical electrical equipment safety and essential performance IEC 60601.1.11 Home healthcare environment USER MANUAL PART NUMBER 50-02-07-200/13 Talley Group Limited Premier Way, Abbey Park Industrial Estate, Romsey, Hampshire, SO51 9DQ England 44(0)1794 503500 +44(0)1794 503555...

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