Celestia CPAP with Heated Humidifier Instruction Manual Model No.: 18250 Please read the instruction manual before use.
Contents Important Safeguards…………………..…………….….….….1 1.Introduction…………………………..........……………….3 2. Product Description……………….…...…………….…..4 3. Installation.………………………………….…...….…….6 4. Operation ……………….............................…………..9 5. Cleaning & Maintenance………………………...…………13 6. Troubleshooting ……….…..…….…………….………...15 7. Technical Specification.………..…….….………..……… 17 8. Note, Caution and Warning Statements……………….….
IMPORTANT SAFEGUARDS SAVE THESE INSTRUCTIONS READ ALL INSTRUCTIONS BEFORE USING WARNING – 1. THIS DEVICE IS NOT INTENDED FOR LIFE SUPPORT. It may stop operating due to power interruption but no hazards to patient. 2. This device should not be used with oxygen. 3. This device should not be used in the vicinity of a flammable anesthetic mixture in combination with oxygen or air and nitrous oxide. 4. The airflow for breathing generated by this device may be as much as 7°C (12.
DANGER -To reduce the risk of electrocution: 1. Always unplug this product immediately after using. 2. Do not use while bathing. 3. Do not place or store product where it can fall or be pulled into a tub or sink. 4. Do not place in or drop into water or other liquid. 5. Do not reach for a product that has fallen into water. Unplug immediately. 6. Do not reach into the water or other liquids, if product falls into water or other liquids. Unplug it immediately.
1. Introduction This manual should be used for initial set up of the system and saved for reference purpose. 1.1 General Information Obstructive Sleep Apnea (OSA) is a condition that an intermitted and repetitive obstruction of the upper respiratory tract causes a complete (apnea) or partial (hypopnea) block of breathing airflow during sleep. The syndrome varies depending on the degree of relaxation of the tongue and soft palate muscle.
2. Product Description Components including: (1) Main CPAP device with integrated heated humidifier (2) Detachable power cord (3) User manual (4) Flexible air tubing with 1.8 m length (5) Full face or nasal mask and headgear straps (Optional, Always use CE certified and 510(k) cleared mask for CPAP) (6) Carrying bag (optional) (7) USB cable and Easy Compliance CD (Optional) Note 1: ONLY for Physician or Technician to download data. Patient should not use this function.
Outlet Port Inlet Port Baffler (Inside Water Chamber) Heater Plate Switch Heater Plate Fill Line Power ON Indicator Removable Base Control Knob Power Socket Heater ON Indicator Water Chamber: Water Chamber Slider The water chamber contains the water for humidification. Its removable base plate allows itself ease for cleaning. Fill Line: Symbol indicates the maximum level of water that water chamber can contain. Baffler: The baffler can prevent water spillage due to improper shaking.
3. Installation 3.1 Unpacking To secure its contents inside, the device and accessories are bundled in a paper packaged box. Unpack this box by removing the device and its accessory and checking for any damage, which may have occurred during shipping. If there are damages, please contact your dealer immediately. 3.2 Setting Up 1) Place the device on a flat surface and at a lower level than your sleeping position. 2) Connect the power cord to the device and plug into main electrical outlet.
4) Connect the other end of the air tubing to the mask system. Putting on the mask and headgear according to the mask instruction manual. Daily Use for the Integrated Humidifier 5) Fill the chamber to the fill line with distilled water (approx. 350 ml). 6) Slide the chamber into place. Make sure the silicon connector on the inlet connector fit securely over the CPAP device air outlet. Note: Make sure the water chamber is pushed to the end to press against the heater plate switch.
3.3 WARNING & CAUTION WARNING: This CPAP machine should be used only with special masks (or connectors) recommended by the manufacturer of the CPAP machine, or by your physician or respiratory therapist. A mask should not be worn unless the CPAP machine is turned on and operating properly. The vent hole associated with the mask should never be blocked for proper exhaling purpose.
4. Operation NOTE: Always read the operating instruction before use. 4.1 Control Panel Description Buttons arrangement on control panel and main use of the buttons: START/STANDBY To start the treatment, simply press the "START/STANDBY" button. To stop the treatment, press the "START/STANDBY" button again. The display will switch between [STANDBY] and Therapy Pressure [ XX.X cmH 2 O] in cmH 2 O unit. MENU Press the "MENU" button to enter the setting mode when device is in standby mode.
4.2 Function Description (1) Ramp Time Ramp time function allows user to fall into sleep with a lower, comfortable pressure and helps users gradually accustomed to increasing treatment pressure. The first selection of pressing "MENU" is [Ramp XX MIN]. When the "MENU" setting is in [Ramp XX MIN] mode, press "UP" or "DOWN" button to set the preferred ramp time and press "MENU" for confirmation. There are 10 adjustable levels, 0, 5, 10, 15, 20, 25, 30, 35, 40 and 45 minutes.
(5) Total Meter Press "MENU" button to select [TM XXXX.X hr] menu, the total compliance meter records the total number of hours that the device has been active. The meter should only be re-set by the provider, a respiratory therapist or by a physician. (6) Compliance Meter Press "MENU" button to select [CM XXXX.X hr] menu, the compliance meter records the total therapy hours for the device. The compliance meter should be re-set only by the provider, a respiratory therapist or by a physician.
4.3 Flowchart of Menu settings Enter the user's menu mode by pressing the “MENU” button. Down Menu Up Ramp (Ramp Time) < 0, 5, 10, 15, ……………., 45> min Ramp P (Ramp Starting Pressure) < 3, 3.5, 4, 4.5, ……………., 17> cmH2O P (Therapy Pressure) < 4, 4.5, 5, 5.5, ……………., 18> cmH2O Alt. (Altitude Compensation) < 1, 2, 3 > TM (Total Meter) < XXXX.X > hr CM (Compliance Meter) < XXXX.
4.4 Using the heated humidifier 1. While the device is turned on., the heater power on indicator on the right side of the device will be lit (green light) 2. Adjust the heater temperature to the desired setting by the control knob.
5.2 Tubing and Mask The tubing and mask should be checked and cleaned daily. Please refer to the cleaning instruction packaged with the accessories. 1. Disconnect the air tubing from the air outlet of the device. 2. Remove the air tubing and headgear straps from the nasal mask. 3. Use a mild detergent and prepare the detergent according to manufacturer's recommendations. Tubing and mask can be washed and rinsed in warm water. 4. Rinse thoroughly and make sure they are completely dry before next use. 5.
and may eventually be replaced. Replace the chamber parts if any damage is present. 6. Troubleshooting The table below lists troubleshooting solutions for the problems that may happen. If the problem persists, contact your equipment provider service agent. P roble m No display P o s s ib l e C a u s e s 1. S o lu t i o ns The power cord is not 1. Ensure the power cord is connected. connected to the power 2. Contact your equipment provider for socket. 2. repair.
Water Leakage close to mask or flexible tube is low. 1. Assembly of water chamber is 1. Remove the water chamber from the heated humidifier, pull out the water and not proper or incorrectly. reassemble the water chamber again, 2. Water chamber or removable make sure the removable base plate is base plate worn out. right fit into water chamber, and fill the water till it reach fill line and check if it still leak or not. 2. Replace a new water chamber. Error / Warning Messages show in LCD.
7. Technical Specifications Ite m Power Supply Sp e c i f i c a t i o n s 16 100-120VAC, 50/60Hz, 0.5A (For 120V system) 220V-240VAC, 50/60Hz, 0.3 A (For 230V system) Therapy Pressure 4 –18 cmH 2 O (adjustable in 0.5 cmH 2 O increment) Ramp Time 0 – 45 minutes (adjustable in 5-minute increment) Ramp Starting Pressure 3 – 17 cmH 2 O (adjustable in 0.5 cmH 2 O increment) Dimensions (W x D x H) 16.5 X 24.5 X13.7 cm Weight 1.4 kg (3.
BF symbol, which indicated this product is according to the degree of protecting against electric shock for type BF equipment. Attention, should read the instructions. Grounding terminal Disposal of Electrical & Electronic Equipment (WEEE): This product should be handed over to an applicable collection point for the recycling of electrical and electronic equipment.
GROUNDING INSTRUCTIONS This product should be grounded. In the event of an electrical short circuit grounding reduces the risk of electric shock by providing an escape wire for the electric current. This product is equipped with a cord having a grounding wire with a grounding plug. The plug must be plugged into an outlet that is properly installed and grounded. DANGER-improper use of the grounding plug can result in a risk of electric shock.
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.
Immunity Test IEC60601 test level Compliance Electromagnetic Environment-Guidance Portable and mobile RF communications equipment should be used no closer to any part of this device, including cables, than there commended separation distance calculated from the equation applicable to the frequency of the transmitter. Conducted RF IEC 61000-4-6 3Vrms150 kHz to 80 MHz outside ISM bandsa 3Vrms Radiated RF IEC 61000-4-3 3 V/m 80 MHz to 2.5 GHz 3V/m Recommended separation distance d = 1.
assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be considered. If the measured field strength in the location in which the device is used exceeds the applicable RF compliance level above, the device should be observed to verify normal operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the device.
Additional instruction for Physician and Technician (Do not distribute to patients) 1. To Set the Therapy Pressure 1. Press "MENU" to select [P XX.XcmH 2 O] menu while in the standby screen. 2. Hold the "UP" and "DOWN" button, and then simultaneously press the "MENU" button for one second. Meanwhile, the LCD screen [P XX.XcmH 2 O] should start blinking to allow you to adjust the therapy pressure from 4 to 18 cm H 2 O. 3. Press "UP" or "DOWN" button to increase or decrease the pressure setting.
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