Drive Medical Celestia 18250 Instruction Manual

Drive Medical Celestia 18250 Instruction Manual

Cpap with heated humidifier

Advertisement

Quick Links

Celestia
CPAP with Heated Humidifier
Instruction Manual
Model No.: 18250
Please read the instruction manual before use.

Advertisement

Table of Contents
loading
Need help?

Need help?

Do you have a question about the Celestia 18250 and is the answer not in the manual?

Questions and answers

Subscribe to Our Youtube Channel

Summary of Contents for Drive Medical Celestia 18250

  • Page 1 Celestia CPAP with Heated Humidifier Instruction Manual Model No.: 18250 Please read the instruction manual before use.
  • Page 2: Table Of Contents

    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……………….…. 18 APPENDIX A: EMC Information……………………………20...
  • Page 3: Important Safeguards

    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.
  • Page 4 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.
  • Page 5: Introduction

    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.
  • Page 6: Product Description

    2. Product Description Components including: Main CPAP device with integrated heated humidifier Detachable power cord User manual Flexible air tubing with 1.8 m length Full face or nasal mask and headgear straps (Optional, Always use CE certified and 510(k) cleared mask for CPAP) Carrying bag (optional) USB cable and Easy Compliance CD (Optional) Note 1: ONLY for Physician or Technician to download data.
  • Page 7 Outlet Port Inlet Port Baffler (Inside Water Chamber) Heater Plate Switch Heater Plate Fill Line Power ON Removable Control Knob Indicator Base Power Socket Heater ON Water Chamber Indicator Slider Water Chamber: The water chamber contains the water for humidification. Its removable base plate allows itself ease for cleaning.
  • Page 8: Installation

    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.
  • Page 9 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.
  • Page 10 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.
  • Page 11: Operation

    4. Operation NOTE: Always read the operating instruction before use. 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 O] in cmH O unit.
  • Page 12 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"...
  • Page 13 (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"...
  • Page 14 Flowchart of Menu settings Enter the user's menu mode by pressing the “MENU” button. Menu Down Confirm Ramp < 0, 5, 10, 15, ……………., 45> min (Ramp Time) Ramp P < 3, 3.5, 4, 4.5, ……………., 17> cmH2O (Ramp Starting Pressure) <...
  • Page 15: Cleaning & Maintenance

    Using the heated humidifier 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. The 1-6 setting corresponds to the temperature as follows: 1 = about 30°C 2 = about 39°C 3 = about 43°C...
  • Page 16 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.
  • Page 17: Troubleshooting

    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 r o b l e m P o s s ib l e C a u s e s S o lu t i o ns No display...
  • Page 18 close to mask or flexible tube is low. Water Leakage 1. Assembly of water chamber is 1. Remove the water chamber from the not proper or incorrectly. heated humidifier, pull out the water and 2. Water chamber or removable reassemble the water chamber again, base plate worn out.
  • Page 19: Technical Specification

    7. Technical Specifications I t e m Sp e c i f i c a t i o n s Power Supply 100-120VAC, 50/60Hz, 0.5A (For 120V system) 220V-240VAC, 50/60Hz, 0.3 A (For 230V system) Therapy Pressure 4 –18 cmH O (adjustable in 0.5 cmH O increment) Ramp Time...
  • Page 20: Note, Caution And Warning Statements

    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.
  • Page 21: Appendix A: Emc Information

    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.
  • Page 22 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. Emissions Test Compliance Electromagnetic Environment-Guidance Harmonic emissions Class A The device is suitable for use in all establishments, including IEC61000-3-2...
  • Page 23 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.
  • Page 24 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.
  • Page 25 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 O] menu while in the standby screen. 2. Hold the "UP" and "DOWN" button, and then simultaneously press the "MENU" button for one second.
  • Page 26 Drive Medical Design & Manufacturing 99 Seaview Boulevard Port Washington, NY 11050 516-998-4600 www.drivemedical.com...

Table of Contents