765000 ALTERNATING PRESSURE MATTRESS SYSTEM WITH ACTIVE SENSOR TECHNOLOGY USER MANUAL Important: Do not operate the Mattress System without first reading and understanding this manual! Save this manual for future use. Info: The most current version of this manual can be found online at www.grahamfield.com.
CONTENTS INTRODUCTION ..................................................................................... 3 INTENDED USE OF THIS DEVICE ........................................................ 3 CONTRAINDICATION...................................................................... 3 IMPORTANT SAFETY PRECAUTIONS .................................................. 4 DANGER ................................................................................................. 4 WARNING ..........................
INTRODUCTION Use this manual for set-up and operation of the Lumex® AltaDyne® Sensor Plus 765000 Alternating Pressure Mattress System with Active Sensor Technology. Read all instructions before using the mattress system. Save this manual for future reference.
IMPORTANT SAFETY PRECAUTIONS The safety statements presented in this chapter refer to the basic safety information that should be observed by those using this Mattress System. There are additional safety statements in other chapters or sections, which may be the same as or similar to the following, or specific to the operations. DANGER: Indicates an imminent hazard situation that, if not avoided, will result in death or serious injury.
WARNING To reduce the risk of burns, electrocution, fire, or personal injury: WARNING: Do not leave this product unattended when plugged in. WARNING: Always use close supervision when this product is used by, on, or near children or those who require close supervision. WARNING: Use this product only as intended and described in this manual. Do not use attachments or accessories not recommended by Graham-Field. WARNING: Never operate this product if: a) It has a damaged cord or plug.
WARNING: Patient entrapment with bed side rails may cause injury or death. The bed frame and its components, including the mattress, bed side rails, head and foot board, bedding, and any accessories added to the bed, can all affect the risk of entrapment. Thorough patient assessment and monitoring are necessary to reduce the risk of entrapment, including establishing whether the use of a bed rail is in the best interest of the patient. Read and understand the User Manual before using this equipment.
EQUIPMENT SYMBOLS Manufacturer “BF”symbol: Indicates that this product is in accordance with the degree of protection against electric shock for type BF equipment Functional earth (for UL only) Attention! Read the instructions! Disposal of Electrical & Electronic Equipment (WEEE): Do not treat this product as household waste.
PRODUCT DESCRIPTION PUMP AND MATTRESS SYSTEM foot end symbol CPR valves mattress pump quick connectors (mattress-pump connectors) pump and mattress system PUMP: FRONT front panel quick connector PUMP: REAR fuse main power switch power cord receptacle 8 hanger filter 765000-INS-LAB-RevC11
PUMP: FRONT PANEL Front panel of pump is shown below. Descriptions of buttons and indicators follow.
Tuning button: The tuning button fine-tunes the mattress system's auto-adjusted pressure. Three tuning settings are available: 0 System auto-adjusted pressure - One level softer than auto-adjusted pressure + One level firmer than auto-adjusted pressure Info: The tuning function is only available in alternate and static therapy modes. Front panel, second row Therapy adjust button: The therapy adjust button selects the therapy mode.
Maxfirm button: The pump will automatically enter maxfirm mode every time the power is turned on. Maxfirm mode ensures the pump is able to reach its maximum operating pressure. Maxfirm mode will last for 20 minutes, and then the system will automatically enter auto-adjust mode. To disable maxfirm mode, press the maxfirm button. When enabled, the maxfirm indicator, at left of button, illuminates.
Low pressure indicator: The low pressure indicator (yellow LED) illuminates, and the alarm sounds, when an abnormally low pressure level occurs. If the low pressure indicator persistently illuminates inappropriately: 1. Check to ensure all connections are properly and securely connected per installation instructions. 2. Check for any leakage (tubes or connecting hoses). If necessary, contact your Graham-Field equipment provider to replace any damaged tubes or hoses. 3.
INSTALLATION UNPACKING 1. Carefully remove all components from the carton. 2. Inspect all components. 3. If damage is evident to the contents, please notify the carrier and your Graham-Field equipment provider. PUMP AND MATTRESS SETUP 1. Place the mattress on top of the bed frame; ensure that the foot end symbol faces up at foot end as shown at right. Secure mattress to bed with straps. hanger 2. Fold open the wire hangers on the back of the pump as shown at right. 3.
WARNING: Locate all cords so that they will not be stepped on, tripped over, or otherwise subjected to damage or stress. WARNING: Do not use a household extension cord if the electrical cord does not reach the power outlet. Use of an improper extension cord could result in fire and electric shock. If an extension cord must be used, use a three conductor cord with ground, properly wired, in good electrical condition, and keep it as short as possible.
OPERATION GETTING STARTED 1. Turn the main power switch to the ON position. 2. Press the front panel power button. The power indicator will illuminate. main power switch power button Info: The mattress system will automatically enter maxfirm mode for the quickest inflation at set-up; when inflated, it will then automatically enter autoadjust mode to select the appropriate pressure. 3. The pump will begin delivering air into the mattress.
TRANSPORT CAP In case of power failure or transport: Disconnect the quick connector and cap the mattress with the transport cap to slow deflation. Info: This system is equipped with cell-on-cell technology to provide added support and prevent bottoming out in the event of a power failure. Lower cells will hold air for approximately eight hours. quick connector transport cap CPR FUNCTION If CPR must be performed on the patient while the mattress is in use, to immediately deflate the mattress, either: 1.
MAINTENANCE CLEANING WARNING: To reduce the risk of increased bacterial growth, infection, illness, or injury from contamination, thoroughly clean and dry the mattress system before use and as necessary during use as follows: Pump: Wipe the pump with a clean, damp cloth and mild detergent, and keep it away from dust. Air dry. s NOTICE: Do not use phenolic products or corrosive or powdered cleansers to clean the pump. s NOTICE: Do not immerse or soak the pump.
Fuse replacement tool needed: small screwdriver 1. If you suspect a blown fuse, disconnect the plug from the wall outlet immediately. 2. Use a small screwdriver to remove the cover of the fuse holder (fuse fuse locations are shown in picture at right). 3. Insert a new fuse of the correct rating (T1A/250V, VDE approved). 4. Replace the fuse holder cover. Ensure that fuse holder cover is securely installed. Air filter replacement tool needed: small screwdriver 1.
SPECIFICATIONS Pump Specification Power Supply (Info: see rating label on product) AC 120V 60 Hz 0.17A (for 120V system) Fuse Rating T1A, 250V Cycle time Fixed / 10 minutes Dimensions (L x W x H) 11.4" x 7.9" x 4.6" (29.1 x 20 x 11.7 cm) Weight 5 lb (2.
LIMITED WARRANTY GF Health Products, Inc. warrants the Lumex® AltaDyne® Sensor Plus 765000 Alternating Pressure Mattress System with Active Sensor Technology for a period of twelve months for defects in workmanship and materials. If a product is deemed to be under warranty, GF Health Products, Inc. shall provide, at its option, (1) replacement of any defective part or product or (2) a credit of the original selling price made to GF Health Products, Inc.'s initial customer.
APPENDIX A: EMC INFORMATION Guidance and Manufacturer’s Declaration- Electromagnetic Emissions: This device is intended for use in the electromagnetic environment specified below. The user of this device should make sure it is used in such an environment.
Guidance and Manufacturer’s Declaration- Electromagnetic Immunity: This device is intended for use in the electromagnetic environment specified below. The user of this device should make sure it is used in such an environment.
a The ISM (industrial, scientific and medical) bands between 150 kHz and 80 MHz are 6,765 MHz to 6,795 MHz;13,553 MHz to 13,567 MHz; 26,957 MHz to 27,283 MHz; and 40,66 MHz to 40,70 MHz. b The compliance levels in the ISM frequency bands between 150 kHz and 80 MHz and in the frequency range 80 MHz to 2,5 GHz are intended to decrease the likelihood that mobile/portable communications equipment could cause interference if it is inadvertently brought into patient areas.
USA Corporate Headquarters: GF Health Products, Inc. 2935 Northeast Parkway Atlanta, Georgia 30360 telephone: 770-368-4700 fax: 770-368-2386 www.grahamfield.com © 2011 GF Health Products, Inc.