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Related Manuals for Proactive Medical Protekt Aire 9900
Summary of Contents for Proactive Medical Protekt Aire 9900
- Page 1 Protekt® Aire 9900 True Low Air Loss Mattress System with Alternating Pressure & Pulsation Instructions For Use Proactive Medical Products 270 Washington Street Mount Vernon, NY 10553 Phone# 1-855-BE-PROACTIVE (855-237-7622) Fax# 845-205-6005 www.proactivemedical.com UML-P1509006-E-2022/04...
- Page 2 IMPORTANT SAFEGUARDS READ ALL INSTRUCTIONS BEFORE OPERATING THIS DEVICE The system has been designed to comply with regulatory safety standards including: ANSI/AAMI ES60601-1 ANSI/AAMI 60601-1-2 NOTE, CAUTION AND WARNING STATEMENTS: NOTE—Indicate some tips. CAUTION—Indicate correct operating or maintenance procedures in order to prevent damage to or destruction of the equipment or other property.
- Page 3 pump has been dropped into water. Return the product to a service center or to the distributor for examination and repair. 8. Keep the power cord away from heated surfaces. 9. Never block the air openings of this product or place the product on a soft surface, such as a bed or couch, where the openings may be blocked.
- Page 4 PRODUCT SYMBOL DESCRIPTION POWER ON POWER OFF ATTENTION CAUTION, READ THE INSTRUCTIONS BEFORE USE IP21 AWAY FROM THE FLAME WATER AND DUST PROTECTION CLASSIFICATION “BF” SYMBOL, INDICATES THIS DISPOSAL OF ELECTRICAL & PRODUCT IS ACCORDING TO ELECTRONIC EQUIPMENT (WEEE): THE DEGREE OF PROTECTION THIS PRODUCT SHOULD BE AGAINST ELECTRIC SHOCK FOR HANDED OVER TO AN APPLICABLE...
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Page 5: Table Of Contents
Contents INTRODUCTION ........................5 INTENDED USE ......................... 5 PRODUCT DESCRIPTION ......................5 PRODUCT INSTALLATION GUIDE ....................6 PANEL DISPLAY AND OPERATION GUIDE ................. 9 CLEANING ..........................16 STORAGE ..........................17 MAINTENANCE ........................17 THE DISPOSAL OF AIR MATTRESS ..................18 TROUBLESHOOTING………………………………………………………………………………………………………….19 TECHNICAL DATA ........................ -
Page 6: Introduction
Instruction for Use. 2. INTENDED USE The Proactive Medical Product’s Protekt® Aire 9900 Mattress System is intended for prevention of pressure ulcers. The Proactive Medical Product’s Protekt® Aire 9900 Mattress System may be used in a variety of settings including, but not limited to individual home care setting and long-term care patients suffering from pressure ulcers, or pain management as prescribed by physician. -
Page 7: Product Installation Guide
4. PRODUCT INSTALLATION GUIDE 1. Unpack the box to inspect all items for any damage that may have occurred during shipping. If there is any damage, please contact your dealer immediately for assistance. 2. Place the mattress on top of the bed frame. The feet symbol on both sides of the mattress indicates location of the foot end. - Page 8 5. Position the pump by its elastic hanger brackets over footboard of the bed. The elastic hanger brackets will self-adjust onto the footboard tightly. 6. Remove the Transport Cap of the hose connector and connect the hose connector to the pump unit. Firmly push the hose connector into position and a “click”...
- Page 9 applied to the mattress recommended by the manufacturer. Do not use the pump for any other purpose. WARNING: Do not place the pump unit in area where power cord can come off easily or inaccessible. 11. For patient’s transportation, press “Auto-Firm”...
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Page 10: Panel Display And Operation Guide
5. PANEL DISPLAY AND OPERATION GUIDE 5.1 PANEL DISPLAY ① Alarm Mute and Alarm Indicator ⚫ Low Pressure Alarm Indicator ⚫ Power Failure Alarm Indicator ⚫ Service (Malfunction) Alarm Indicator ② Alternate/Pulsate Cycle Time Selection or Warning Code Display ③ Operating or Standby ④... - Page 11 5.1.3 Operate or Standby Press this button to start operating or go into standby. 5.1.4 Auto-Firm The pump will go into the inflation mode (LED lights flashing) every time the operate mode is triggered. This ensures the mattress to be able to reach its maximum operating pressure.
- Page 12 recommendation. 5.1.8 Comfort Control Comfort controls the air pressure output level. Press Firm button and the output pressure will increase and higher pressure output will support heavier weight patient, for decreasing air pressure, vice versa. Check to see if the suitable pressure is selected by sliding one hand between a deflated air cell and the patient’s buttocks areas and there should be minimum contact.
- Page 13 ⚫ According to the weight of the patient, adjust the pressure setting to the most suitable level without “bottoming-out”. User can determine an appropriate pressure by adjusting the Comfort Level. Please consult with your physician for a proper setting. WARNING: The pump unit should always be operating to prevent pressure injury from occurring.
- Page 14 Protekt® Aire 9900 & 81090-42, 81090-48, 81090-54, 81090-60 5.2.2 CPR When CPR needs to be performed, quickly rotate the CPR valve to “OPEN” position, at the same time, disconnect the hose connector from the pump to speed up the air release. 5.2.3 Audiovisual Alarm ⚫...
- Page 15 NOTE: Refer to Table 2 for Warning Code Reference if error code appears on the display or refer to 10. TROUBLESHOOTING 5.2.4 Alarm Mute ⚫ When alarms are triggered, both LED light and buzzer will turn on to warn the patient and caregiver.
- Page 16 Table 2 Warning Code Reference PRIORITY HIGH WARNING INDICATOR AUDIBLE OUTPUT WARNING DESCRIPTION REMARKS ↓ CODE MODE Key Tone from Functional ONCE Key Tone Buttons Power Failure ONCE Shutdown Shutdown ALL LED ONCE All Indicators On Power-On ONCE No Display State/Mode Switching Auto-Firm ONCE...
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Page 17: Cleaning
6. CLEANING Wipe the pump unit with a damp cloth pre-soaked with a mild detergent and keep the pump unit away from dust. If other detergent is used, choose one that will have no chemical effects on the surface of the plastic case of the pump unit. CAUTION: Do not immerse or soak the pump unit. -
Page 18: Storage
damage to the mattress cover. CAUTION: Do not use phenolic-based product for cleaning. CAUTION: After cleaning, dry the mattress without direct exposure of sunlight. 7. STORAGE ⚫ Rotate the CPR valve to OPEN position and disconnect the hose connector to release the air. -
Page 19: The Disposal Of Air Mattress
⚫ Insert a new fuse in the correct rating and replace the cover of the fuse holder. The fuse rating should comply with the requested specification. Air Filter Replacement After checking 10. TROUBLESHOOTING, if the air filter needs to be replaced: ⚫... -
Page 20: Troubleshooting
10. TROUBLESHOOTING PROBLEM SOLUTION ⚫ The mattress is not able to Check if the mattress model (model no. located inside the cover by connect with the pump the foot end) xxAAAxxx matches with the pump model xxBBB-xxx. The AAA should be the same as BBB. If not, please contact with the agent or distributor. -
Page 21: Technical Data
11. TECHNICAL DATA 11.1 PRODUCT SPECIFICATION PUMP UNIT AIR MATTRESS Model 81090 Model 8” Mattress Dimension (cm) 40 (W) x 17.5 (D) x 27.5 (H) Dimension (cm) 200 (L) x 90 (W) x 20(H) 200 (L) x 107 (W) x 20 (H) 200 (L) x 122 (W) x 20 (H) 200 (L) x 137 (W) x 20 (H) 200 (L) x 153 (W) x 20 (H) - Page 22 Transport & Storage Conditions -25 °C to 70 °C; 10 % to 90 % RH Altitudes ≤ 3000 m Degree of Protection Against Ingress IP21...
- Page 23 11.2 EMC INFORMATION WARNING: Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation. If such use is necessary, this equipment and the other equipment should be observed to verify that they are operating normally.
- Page 24 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-...
- Page 25 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...
- Page 26 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.
- Page 27 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 Maximum...
- Page 28 Proactive Medical Products 270 Washington Street Mount Vernon, NY 10553 Phone#: 1-855-BE-PROACTIVE Ph#: (855-237-7622) Fax#: 845-205-6005 www.proactivemedical.com...
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