Contents Introduction ............................5 Intended Use ............................ 5 2.1 Contraindications ........................5 About the Product ..........................5 Symbols and Statements ......................... 7 Important Safety Information ......................8 Technical Specification ........................9 6.1 Power unit ..........................9 6.2 Mattress ........................... 9 Installation and Set-Up........................
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15.2 Fuse replacement ........................21 15.3 Air filter replacement ......................21 16. EMC Information ..........................22 Page 4 of 29 Issue: 4 - 16/08/18...
User Manual. Note: Ultimate Healthcare reserves the right to modify the information in this User Manual at any time. The information in this User Manual may vary slightly with respect to the basic design of the product.
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Mattress Replacement HEAD END 3 x Static Head Cells Knitted Cell Retention Bands Removable Cover CPR Tag 1 x Standard Cell 11 x Standard Cells FOOT END 4 x Smaller Lower Legs Cells (TPU) Cable Management Fixings Air Pipe Connector Power Unit Carry Handle Air Pipe...
4. Symbols and Statements Note: Indicates tips and advice for the correct use of this product. Caution: Indicates correct operating or maintenance procedures in order to prevent damage to or destruction of the product or other property. Warning: Indicates potential danger that requires correct procedures or practises in order to prevent personal injury.
Use only the cleaning and disinfectant agents recommended in this User Manual. When connecting product after transportation or storage, inspect the power cable visually for any signs of damage. If evident, do not use product and contact Ultimate Healthcare or your local distributor for repair.
6. Technical Specification Power unit Dimensions: 130mm x 420mm x 230mm (D x W X H) Weight: 4.6 kg Alternating cycle time: 10 / 15 / 20 / 25 / 30 mins Output pressure range: 25 to 60mmHg (+/-2) Power supply: AC 230V 50 Hz Current: 3.0 amp...
7. Installation and Set-Up Setting up mattress For the comfort and safety of the patient do not put them onto the mattress until you are sure that the mattress is properly secured and the system indicates that it is fully inflated. The mattress is designed to completely replace any existing mattress which may be in use on a bed.
Cable management system Cable management fixings are located on each side of the mattress underneath the flap of the cover. The mains power cable should be secured through the cable management fixing as follows: Locate each cable management fixing. ...
8. Control Panel Operation Guide The Control Panel of the power unit is used to make adjustments to the mattress and also indicates fault conditions/service requirements. These are either visual (indicator lights) or audible. Auto detection Auto-Firm & Indicator Comfort Control Buttons Operate / Standby Button &...
Comfort level The Soft and Firm buttons allow carers to adjust pressures within a safe pre-set range to provide patients with enhanced comfort or support whilst maintaining a very good level of protection and therapy. Qualified clinical advice must always be taken before adjusting mattress pressures.
Function mode switch 8.5.1 Alternate Alternating mode is the default mode for the system. Within this mode the mattress will operate in an alternating 1-in-2 cell cycle. The alternating cycle will continue at the selected cycle time until another mode is selected. 8.5.2 Static Pressing the Function Mode Selection button until the Static indicator illuminates puts the system into Static mode.
9. CPR Mode CPR (Cardio Pulmonary Resuscitation) can be performed using the red CPR valve which is situated at the head end on the left hand side of the mattress. For rapid deflation gently pull and rotate the dial of the CPR valve to ‘click’...
11.3 Service (alternating failure alarm) Should your system develop a fault condition whilst in use, an audible alarm will be heard and the Service indicator will illuminate. Please refer to Table 1 for error codes and call Ultimate Healthcare or your local distributor.
REPEAT Operate or Low Pressure Low Pressure Pressure Standby Overtime Alarm (Cycle 4 sec) REPEAT Operate or High Pressure Service High Pressure Standby Overtime Alarm (Cycle 4.5 sec) REPEAT Operate or High Ambient Service High Temperature Standby Temperature Alarm (Cycle 4.5 sec) REPEAT Operate or Air Valve 1 Positioning...
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Indicates that system is scheduled for an annual Service indicator remains service. Please contact Ultimate Healthcare or your illuminated local dealer to arrange. If the problem persists, contact Ultimate Healthcare or your local service provider. Page 18 of 29 Issue: 4 - 16/08/18...
Healthcare cannot be held liable for. Caution: The appropriate qualified staff must be consulted when specifying a suitable cleaning fluid. Ultimate Healthcare shall not be liable for any damages caused by the use of inappropriate detergents or disinfectants. 13.2 Mattress and cover disinfection...
13.3 Power unit disinfection The power unit can be cleaned by wiping down with a cloth dampened with hot water at 60 containing detergent or with sodium hypochlorite (up to 10,000 parts per million available chlorine). 13.4 Cover laundering The mattress cover and air pipe cover can also be machine washed. Mattress covers and air pipe cover should be completely removed prior to laundering.
15. Service and Maintenance It is recommended that this product be part of a routine preventative maintenance schedule with a planned service every 12 months regardless of product usage. The Heritage II Digital features a dedicated Annual Service indicator on the control panel which will illuminate and stay ON to alert nursing staff of the need for the system to be professionally serviced.
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16. EMC Information Guidance and manufacturer’s declaration-electromagnetic emissions The GD311-401 is intended for use in the electromagnetic environment specified below. The customer or the user of the GD311-401 should assure that it is used in such an environment. Emission test Compliance Electromagnetic environment-guidance RF emissions...
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Guidance and manufacturer’s declaration-electromagnetic immunity The GD311-401 is intended for use in the electromagnetic environment specified below. The customer or the user of the GD311-401 should assure that it is used in such an environment. Immunity test IEC 60601 Compliance level Electromagnetic test level environment-guidance...
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Guidance and manufacturer’s declaration-electromagnetic immunity The GD311-401 is intended for use in the electromagnetic environment specified below. The customer or the user of the GD311-401 should assure that is used in such and environment. Immunity test IEC 60601 test level Compliance level Electromagnetic environment-guidance Portable and mobile RF communications...
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Recommended separation distance between portable and mobile RF communications equipment and the GD311-401 The GD311-401 is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of the GD311-401 can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the GD311-401 as recommended below, according to the maximum output power of the communications equipment.