HELP WITH SAFETY CARE For every type of use, Hillrom™ mattresses provide patients with optimal comfort and greater independence for a feeling of well-being that is conducive to a swift recovery. They are also easy to use for caregivers. (6) - 199253 Accella™...
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Understanding the Symbols Symbol Description Highlights special information or explains important instructions. WARNING This symbol indicates that the failure to follow the associated recommendation can put the patient or the user in danger, or damage the equipment. CAUTION This symbol indicates that the failure to follow the associated recommendation can result in damage to the equipment.
Safety and Usage Tips Intended Use This device benefits are phase I to phase IV pressure ulcers prevention and treatment help. Indications It is suitable for low to very high-risk patients, within the recommended patient weight limits of 30 to 160 kg on the standalone mattress and between 40 and 160 kg on the version combined with the Accella™...
Accella™ Therapy MCM™ mattress P006791A* P006794A* P006789A* Accella™ Therapy MCM™ mattress combined with Hillrom™ 900 Accella™ bed P006792A* P006793A* Accella™ Therapy MCM™ mattress combined with Hillrom™ 900 Progressa™ bed The mattress P006783A or P006788A or P006790A or P006791A is a standalone mattress controlled by a wired remote control,also available as an accessory (see page 51).
Preventing Risks Improper use of the device can result in risks for the patient or the user. The following recommendations must be read and followed. In view of the multitude of models of frames and siderails, and for safety reasons, Hill-Rom advises that all necessary precautions must be taken, especially with regard to the height of the siderails and the dimensions of the mattress support platform.
For the mattress P006789A* or P006792A* (combined with the Accella™ bed) and P006793A* (combined with the Progressa™ bed), refer to the bed’s manual for the recommendations on connections. In compliance with standards relating to electromagnetic interference for medical devices, this product does not interfere with other medical devices nor is it susceptible to interference when combined with other medical devices that also comply with the electromagnetic standards in place.
Referring to Technical Specifications Specifications are subject to change. Essential performances of the device The Accella™ Therapy is a therapeutic mattress. It has two operating modes: continuous low pressure (CLP) and alternating low pressure (ALP), with permanent regulation of the pressure by the I-mmersion™ sensor in both modes. Control pendant* Front View of the Control Pendant Control...
Therapeutic Mattress Characteristics Description P006783A- P006790A- P006793A- Model P006788A- P006791A- P006794A P006789A P006792A 215x96x21.5 cm Dimension (inflated) 203x92x21.5 cm / 80x35.5x8.5’’ / 84.6x37.8x8.5’’ Weight ~ 17.5 kg / ~ 37.5 lb Voltage 220-240V 120V 220-240V Frequency 50 Hz 60 Hz 50 Hz Apparent power ALP &...
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Viewing the Whole Device Item Name Upper cover Therapeutic Mattress with 5 Zones: Head zone (3 bladders) Back zone (6 bladders) Sacrum zone (8 bladders) Thigh zone (2 bladders) Heel Zone (11 bladders) Bottom Cover I-mmersion™ sensor Straps (Accella™ Therapy) or knobs (Progressa™) Technical box Bottom cover Control pendant*...
Understanding the Symbols on the Device Symbols on the Upper Cover Do not walk on or run over the power cord Adjust the straps Foot end Zone for notes Always install the mattress so that the (I-mmersion™ ) Therapy text is visible Seat cushion X-ray bag MCM™...
Symbols on the Technical Box fuse 220-240VAC: 5*20 time delayed 1.6A fuse-Icu=1,500A 120VAC: 5*20 time delayed 2A fuse-Icu=1500A (6) - 199253 Accella™ Therapy Mattress Instructions for Use Page 11...
Symbols on the Control Pendant* All commands are centralized and are activated by simply pressing a button. Buttons and indicator lights Symbol Description Symbol Description CPR activated: Green 6 On/Off Button Continuous low Malfunction/service alarm: pressure (CLP) mode yellow and intermittent activated: Green audible alarm Mains power present after...
Symbols on the labels Cover protected against access to dangerous Manufacturer IP24 parts with fingers and splashes of water Type BF applied parts protected against Device reference defibrillation shocks Serial number Class II device Medical Device Alternating Current conformity mark General safety sign Temperature limits Refer to the user...
Locating the Identification Labels of the Device On the technical box To identify the device model REF and its serial number SN: P006783A P006788A P006789A P006790A P006791A P006792A P006793A P006794A (6) - Page 14 199253 Accella™ Therapy Mattress Instructions for Use...
On the Control Pendant The label showing the conditions of use and specifications of the device is located on the rear of the control pendant. Refer to “Symbols on the labels” page 13 for details of the symbols. Accessing to the Upper and BottomCovers Identification Labels Open the zip fastener on the device Upper cover P006788A-P006789A-...
See details of the symbols for cleaning and disinfection in the “Disinfecting and Servicing” page 39 section. Checking the Model of the Device on the Packaging Label P006783A P006788A P006789A P006790A P006791A P006792A P006793A P006794A See symbols in paragraph“Complying with Conditions for Transport, Storage and Use”...
Installing the Patient Before Placing the Patient on the Device Assess the various risks, including but not limited to the following (incomplete list containing risks related to reasonably foreseeable misuse): • risk of entrapment; • potential falls from the bed; •...
Installing the Device Standalone version 1. Unpack the control unit and the mattress. Take care not to damage them when unpacking. 2. Check that all the components are present and correct, and that the power cord is not damaged. 3. Place the rolled up mattress on the top of the bed at head foot end and unroll it.
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9. Attach the control pendant to the footboard of the bed using the handle attachment (A). 10. Open the zip fastener of the upper cover on the left at the foot of the bed. Pass the cord through the hole in the middle on the left-hand side and put the power cord under the lower mattress and the connector as shown below, making sure that it is secured by the safety clamp (B).
15. Close the zip on the upper cover. Placing a cotton sheet on the mattress will improve patient comfort and make it easier to administer care. It is advisable not to place any waterproof materials (e.g., drapes) on mattresses with the MCM™ function, as doing so would reduce the performance of the function.
8. Connect the plug to the bed connector (it clicks into place). 9. Install the hard surface of the thigh section. 10. Attach the mattress using the straps in the center on the thigh section. 11. Unfold the mattress. 12. Adjust the length of the straps to securely attach the mattress.
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3. Place the rolled up mattress on the top of the bed at the head end and unroll it. 4. Check that the symbol on the cover is at the foot of the bed. Fold in two at the head end. 6.
Mobilizing and Securing the Patient The CPR function and the therapeutic modes and alarms are not available when the mattress is OFF. This device is designed for optimal therapeutic benefits when the adjustable head section is inclined to between 0° and 45°. Raising the head of bed to 45°...
After 20 minutes, the device automatically returns to the initial therapy mode to reduce the risks associated with non-therapy mode. After activating the P-Max mode, it is possible to return to therapy mode previously selected by selecting the P-Max button. Transport mode The Accella™...
Combined mattress Refer to the bed’s manual for the activation and control of the different therapeutic modes. Activating the CPR Standalone version In emergencies, opening the CPR valve (cardiopulmonary resuscitation) quickly deflates the mattress, providing a hard surface for external heart massages. Do not allow unqualified persons to activate this function.
X-ray cassette pouch The head end of the mattress is equipped with a pouch for X-ray cassettes (min. height 85 cm, min. width 84 cm) to take chest X-rays. The type of materials, the density and the thickness of the mattress, and the weight and morphology of the patient can affect the quality of the X-ray images.
Understanding the Alarms Meaning of the alarms on the standalone mattress* Type of Time before Action to be taken by Reason for sounding alarm sounding the operator When the product starts: Calibration problem, battery Audible Immediate Contact a Hill-Rom missing, low battery, and visible technician I-mmersion™...
Table of alerts Type of Time before Action to be taken by Reason for sounding alarm sounding the operator Immediately, at the end of the At the end of the product Audible (1 product Mattress ready for use initialization phase beep) initialization phase...
Mains power fault The audible Mains power fault alarm sounds and the corresponding yellow visual alarm comes on if the device is disconnected from mains, or in the event of a power failure. The audible and visual alarms remain active during the transport of the device. (see “Moving the Patient on the Bed in Transport Mode”...
Moving the Device Moving the Patient on the Bed in Transport Mode 1. Unplug the device from the wall socket. Never pull on the power cable or you may damage it. A damaged power cord is an electric shock hazard. The device automatically switches to transport mode.
Transferring the Device from One Bed to Another Never leave the patient on the device during transfer. Make sure that the bed chassis brakes are applied to prevent any accidental movements. Standalone version* 1. Activate the maximum inflate mode and wait for 1 minute, until the mattress is firm.
Storing the Device Make sure that the bed chassis brakes are applied to prevent any accidental movements. Deflating the standalone mattress* 1. Open the head end zip fastener. Unscrew and remove the deflation plug (A). 2. Undo the two straps that secure the mattress to the bed (at the head and foot ends) for the Accella™...
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11. Use the strap on the lower cover to keep the mattress rolled up. 12. Place the rolled up mattress in a plastic bag. 13. Store the mattress in its original packaging or in a transport bag. Deflate the mattress combined with the Accella™* bed 1.
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10. Starting at the foot end of the bed, roll up the mattress slowly to allow any remaining air to be expelled. 11. Expel as much air as possible. 12. Screw in the deflation plug. 13. Close the zip fastener. 14.
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7. Open the head end zip fastener. Unscrew and remove the deflation plug (A). 8. Starting at the foot end of the bed, roll up the mattress slowly to allow any remaining air to be expelled. 9. Expel as much air as possible. 10.
Disinfecting and Servicing Cleaning and Disinfecting the Device Complying with Safety Instructions • Check that the brakes are applied on the bed on which the mattress is installed. • Lock out all electrical functions. • Disconnect the appliance and stow the power cable. •...
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Using cleaning and disinfecting protocols or products other than those recommended by Hill-Rom can compromise the conformity of the device and patient safety and render the warranty null and void. Hill-Rom recommends that the device should be disinfected before scrapping, in accordance with applicable local regulations.
Cleaning and disinfection frequency of the various parts of the mattress Parts to be kept clean at all times. - After a patient’s departure. - At every change of sheets if the inspection reveals ingress of fluids. Cleaning and Disinfecting after the Departure of a Patient or when Changing the Sheets Using Recommended Products Disinfectant detergent at and recommended contact time and dilution...
For all other disinfectants: Chlorine-based solutions can be used. Concentration must be less than or equal to 1,000 ppm. Ethanol-based solutions (alcohol) can be used. Concentration must not exceed ¼ of ethanol for ¾ of water. Proceed with the final steps before reusing the cleaned and disinfected mattress (see “Proceed with the final steps before reusing the cleaned and disinfected device.”...
The upper cover can be machine-washed, but it must not always be machine-washed, as doing so will reduce the life time of the components. The upper cover should only be machine-washed if particular risks of infection occur. If this method is used, choose the wash and spin cycle with reduced mechanical action.
Servicing of the Device Complying with Safety Instructions Never modify this device without Hill-Rom's prior written consent. Only facility-authorized personnel should perform maintenance. Changes made by unauthorized personnel may result in damage to the device and/or serious injury to staff or users. Before maintenance or servicing works: •...
Troubleshooting The device is designed to adjust automatically, therefore troubleshooting is limited to a few checks. Always disconnect the device before troubleshooting. In the event of a malfunction, press the silence alarm button to stop the audible alarm. Check the following points: •...
Complying with Warranty Conditions The warranty for Hill-Rom’s devices will be rendered null and void, in part or in total, in the event of: • Repairs, installations, assembly, modifications or checks and tests are not conducted by the manufacturer’s maintenance personnel or by personnel authorized by the manufacturer.
Accessories and additional parts Reflex Seat Cushion (M04177)** ™ The seat cushion is available as an option with the Accella™ Therapy device. In combination with the air mattresses, the ReFlex™ seat cushion provide 24-hour pressure relieving care and help to prevent pressure ulcers for semi-mobile patients up to high.
Locate the seat cushion labels On the seat cushion cover. Open the zip fastener of the device. Identification labels Packaging labels (6) - Page 48 199253 Accella™ Therapy Mattress Instructions for Use...
Installing the Seat Cushion 1. Open the flap (B) on the seat cushion, disconnect and stretch the spiral hose (C). 2. Lift the cover of the device at the foot left end to access to the zip fastener (E). 3. Open the zip fastener to locate the seat cushion’s outlet between the two mattresses.
11. Select the Continuous Low Pressure mode on the control pendant. Once the patient is back on the mattress, the sensor automatically adjusts and provides optimal pressure management of the mattress. Deflating and Packing the Seat Cushion 1. Open the closure located adjacent to the protection of the hose. 2.
Control pendant** A control pendant can be ordered for the device. Model Description AD293A** Control pendant for mattress P006788A or P006791A (low pressure Accella™ Therapy MCM™ mattress) AD313A** Control pendant for mattress P006783A or P006790A (low pressure Accella™ Therapy mattress) Correlation mattress / control pendant P006788A/ P006783A/...
Compliance Electromagnetic Compatibility Compliance CE conformity mark The CE conformity mark applicable to class IIa Medical Devices was applied to the Accella™ Therapy mattress for the first time in 2018. Standards Designation EN 60601-1: 2007 / A1: 2017 IEC 60601-1: 2005 / A1: 2012 EN 60601-1-2: 2015 IEC 60601-1-2: 2014 EN 60601-1-6: 2010...
Electromagnetic emissions compliance Manufacturer's recommendations and declaration – electromagnetic emissions The Accella™ Therapy mattress is intended for use in the electromagnetic environment specified below. The customer or the user of the Accella™ Therapy mattress device should make sure it is used in such an environment. Emission test Compliance Electromagnetic environment...
Manufacturer's recommendations and declaration – electromagnetic immunity The Accella™ Therapy device is intended for use in the electromagnetic environment specified below. The customer or the user of the Accella™ Therapy device should make sure it is used in such an environment. Immunity test Test level Compliance...
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RF communication equipment (including peripherals such as antenna cables and external antennas) should be used no closer to any part of the device, including cables specified by Hill-Rom, than the recommended separation distances shown in the following table. Otherwise, degradation of the performance of this equipment could result. Wireless communication system Separation distance...
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Table 6 – Recommended separation distances between portable and mobile RF communication equipment and Accella™ Therapy device –for the Accella™ Therapy device Recommended separation distances between portable and mobile RF communications equipment and the Accella™ Therapy The Accella™ Therapy device is designed for use in an electromagnetic environment in which interference due to radiated RF is monitored.
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