Contents Introduction ............................5 Intended Use ............................ 5 2.1 Contraindications ........................5 One in Three ............................ 5 About the Product ..........................5 Symbols and Statements ......................... 7 Important Safety Information ......................8 Technical Specification ........................9 7.1 Pump............................9 7.2 Mattress ........................... 9 Installation and Set-Up........................
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16.1 General ..........................21 16.2 Fuse replacement ........................21 16.3 Air filter replacement ......................21 17 EMC Information ..........................22 Issue 5: 07/01/2021 Page 4 of 28...
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 4 x Static Head Cells (TPU) HEAD END Knitted Cell Retention Bands CPR Valve Removable Cover Figure of 8 cell technology 20 x Alternating Cells (TPU) Cable Management Fixings FOOT END Air Outlet port Issue 5: 07/01/2021 Page 6 of 28...
Pump Carry Handle Control Panel Swing Out Bed Hooks Air Outlet Port ON/OFF Switch Power Connection 5. 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.
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.
7. Technical Specification Pump Dimensions: 130mm x 320mm x 230mm (D x W x H) Weight: 3.5 kg Alternating cycle time: 10 / 15 / 20 / 25 / 30 mins Output pressure range: 15 to 50mmHg (+/-10%) Power supply: AC 230V 50 Hz Current: 0.12 A...
8 Installation and Set-Up Setting up mattress Secure the mattress to the moving parts of the bedframe using the securing straps, and when the system is fully inflated it is ready for the patient to be positioned onto the mattress. 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. ...
9 Control Panel Operation Guide The Control Panel of the Pump is used to make adjustments to the mattress and also indicates fault conditions/service requirements. These are either visual (indicator lights) or audible. Comfort Control Buttons Auto-Firm & Indicator Comfort Setting Indicators 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 9.5.1 Alternate Alternating mode is the default mode for the system. Within this mode the mattress will operate in an alternating 1-in-3 cell cycle. The alternating cycle will continue at the selected cycle time until another mode is selected. 9.5.2 Static Pressing the Function Mode Selection button until the Static indicator illuminates puts the system into Static mode.
This will maintain the cells in their present state for up to 24 – 48 hours. It is important to restore the Tamora III Advance dynamic replacement mattress as quickly as possible by reconnecting the supply tubes to the Pump.
12. Alarms Fault Findings The Tamora III Advance is equipped with audible and visual alarm indicators. These alert the user to the status of the available mains supply and any mattress defect. 12.1 Low pressure alarm Upon detection of low pressure, an audible alarm will be heard and the Low Pressure indicator will illuminate.
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Table 2: Alert/Error Code Reference Table Priority High Warning Indicator Audible Output Condition of Warning Description Remarks ↓ Code Mode Output Not in System Key Tone from ONCE Key Tone Shutdown Functional Button Power Failure ONCE Power-Off System Shutdown Shutdown Operate or All Indicators ALL LED...
Indicates that system is scheduled for an annual Service indicator remains service. Please contact Ultimate Healthcare or your illuminated local service provider to arrange. If the problem persists, contact Ultimate Healthcare or your local service provider. Issue 5: 07/01/2021 Page 18 of 28...
14.2 Mattress and cover disinfection The Tamora III Advance mattress, mattress cover and air pipe cover can be cleaned using the following simple procedures in accordance with your Local Infection Control Policy: ...
14.3 Pump disinfection The Pump can be cleaned by wiping down with a cloth dampened with hot water at 60 C containing detergent or with sodium hypochlorite (up to 10,000 parts per million available chlorine). 14.4 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.
12 months regardless of product usage. The Tamora III Advance 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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17 EMC Information Manufacturer’s declaration-electromagnetic emissions The device(s) is intended for use in the electromagnetic environment (for home and professional healthcare) specified below. The customer or the user of the device(s) should assure that it is used in such an environment.
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Manufacturer’s declaration-electromagnetic immunity The device(s) is intended for use in the electromagnetic environment (for home and professional healthcare) specified below. The customer or the user of the device(s) should assure that it is used in such an environment. Immunity test IEC 60601 Compliance level Electromagnetic environment-...
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Manufacturer’s declaration-electromagnetic immunity The device(s) is intended for use in the electromagnetic environment (for home and professional healthcare) specified below. The customer or the user of the device(s) should assure that it is used in such and environment. Immunity test IEC 60601 test level Compliance level Electromagnetic environment-guidance...
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Recommended separation distance between portable and mobile RF communications equipment and the device(s) The device(s) is intended for use in an electromagnetic environment (for home and professional healthcare) in which radiated RF disturbances are controlled. The customer or the user of the device(s) can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and the device(s) as recommended below, according to the maximum output power of the communications equipment.
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Manufacturer’s declaration-electromagnetic immunity Test specifications for to RF wireless communications equipment ENCLOSURE PORT IMMUNITY The device(s) is intended for use in the electromagnetic environment (for home and professional healthcare) specified below. The customer or the user of the device(s) should assure that it is used in such an environment. Compliance LEVEL Test...
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Notes: Issue 5: 07/01/2021 Page 27 of 28...