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Summary of Contents for Drive Medical Oxus
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Portable Oxygen Concentrator User Manual Reliability Reliability Plus Plus...
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Oxus. Before using any Oxus product, be sure to read (except for brief excerpts in reviews and scientific papers), without the prior carefully and understand all manuals provided with the product.
Classification This equipment is listed with a nationally recognized testing laboratory and classified with respect to electric shock, fire, and mechanical hazards in accordance with the following standards: • E N 60601-1 (1990), Medical Electrical Equipment, Part 1: General Requirements for Safety +A1(1993) +A2(1995) +A13(1996) • U L 60601-1 (1st edition, 2006-04-26), Medical Electrical Equipment, Part 1: General Requirements for Safety • I EC 60601-1 (2nd edition), Medical Electrical Equipment, Part 1: General Requirements for Safety, with A1 and A2 • C AN/CSA C22.2 No. 601.1-M90 (R2005), Medical Electrical Equipment, Part 1: General Requirements for Safety • I EC 60601-1-4 (2000-2004), Edition 1.1 Consolidated Edition, Medical...
WARNING: Do Not Remove Filter No Open When Unit is Operating No Oil Do not Keep Smoking Flame or Grease Disassemble WARNING: Do Not Remove Filter Explanation of Packaging and No Open When Unit is Operating No Oil Keep Do not CAUTION: Consult Smoking...
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CAUTION: Consult accompanying documents 6.7A Do not use if packaging is damaged = 87% - 96% Oxygen Handle with care Date of manufacture Manufacturer name and address Rochester Hills, MI 48309 Keep dry (This symbol refers to the IPX2 WARNING: Do Not Remove Filter classification of the device) When Unit is Operating No Oil Do not Keep or Grease Disassemble Artwork, Product Label, Matchbox CAUTION: Consult Dispose of used battery properly...
Introduction MANUAL VERSION Please refer to this manual for detailed instructions on warnings, precautions, specifications, and additional information. Printed in U.S.A. GENERAL INFORMATION This user manual provides information for users of the Portable Oxygen Concentrator. For the sake of brevity, the terms “concentrator,” “unit,” or “device” are sometimes used in this document to refer to the Portable Oxygen Concentrator. IMPORTANT: Users should read this entire manual before operating the Portable Oxygen Concentrator. Failure to do so could result in personal injury and/or death. If you have questions about the information in this user manual or about the safe operation of this system, contact your distributor.
INDICATIONS FOR USE The Portable Oxygen Concentrator is intended to provide supplemental oxygen in a home, institutional, or travel environment. INTENDED USE The Portable Oxygen Concentrator is intended to deliver concentrated oxygen for adult patients with chronic pulmonary diseases such as chronic bronchitis, emphysema, asthma, or lung cancer, those in the terminal stage of cancer, or any patient requiring supplemental oxygen. The device is portable, enabling patients who need an oxygen device to be treated at home according to a clinician’s prescription or direction. The Portable Oxygen Concentrator is a prescription-only device, is not intended for use in life-supporting or life-sustaining situations, and is provided non-sterile. It is designed to be used indoors or outdoors. CONTRAINDICATIONS The Portable Oxygen Concentrator is not intended to be used: • in life-supporting or life-sustaining situations • in an operating or surgical environment • with a non-adult population...
Warnings and Precautions WARNINGS OVERVIEW WARNING: 1. CRITICAL! EXPLOSION HAZARD. DO NOT USE IN THE PRESENCE OF FLAMMABLE ANESTHETICS! 2. DO NOT USE A PORTABLE OXYGEN CONCENTRATOR OR ANY ACCESSORY THAT SHOWS ANY SIGN OF DAMAGE. 3. DO NOT ALLOW SMOKING OR OPEN FLAMES NEAR THIS DEVICE.
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PRECAUTION: 4. IF YOU ARE UNABLE TO HEAR OR SEE ALARMS, DO NOT HAVE NORMAL TACTILE SENSITIVITY, OR CANNOT COMMUNICATE DISCOMFORT, CONSULT CLINICIAN BEFORE USING THIS DEVICE. 5. THIS DEVICE IS NOT DESIGNED FOR USE WITH A HUMIDIFIER OR NEBULIZER. IF A HUMIDIFIER OR NEBULIZER IS USED WITH THIS DEVICE, PERFORMANCE MAY BE DIMINISHED AND THE DEVICE MAY BE DAMAGED. 6. PATIENTS WITH A FAST BREATHING RATE REQUIRING A HIGHER OXYGEN SETTING MAY REQUIRE MORE OXYGEN THAN THIS DEVICE CAN PRODUCE. THIS DEVICE MAY NOT BE APPROPRIATE IN THAT CASE. CONSULT CLINICIAN FOR ALTERNATIVE TREATMENT. 7. ONLY USE APPROVED ACCESSORIES WITH THIS DEVICE. REFER TO THE APPROVED ACCESSORIES GUIDE FOR A COMPLETE LIST OF ACCESSORIES AND CANNULA APPROVED FOR USE WITH THIS DEVICE. USING UNAPPROVED ACCESSORIES OR CANNULA MAY IMPAIR THE PERFORMANCE OF THIS DEVICE. 8. REPLACE THE CANNULA ON A REGULAR BASIS. CHECK WITH your distributor OR CLINICIAN TO DETERMINE HOW OFTEN THE CANNULA SHOULD BE REPLACED. 9. ELECTRICAL CORD AND/OR TUBING LYING ON THE FLOOR COULD PRESENT A TRIPPING HAZARD. 10. NEVER LEAVE THIS DEVICE IN A HOT ENVIRONMENT. NEVER LEAVE THIS DEVICE IN A LOW-TEMPERATURE ENVIRONMENT. EXTREME HIGH OR LOW TEMPERATURES CAN DAMAGE THIS DEVICE. 11. IF OXYGEN CONCENTRATION DROPS BELOW THE SPECIFIED LEVEL, AN ALARM WILL INDICATE THIS CONDITION. IF ALARM PERSISTS, STOP USING THIS DEVICE, SWITCH TO AN ALTERNATE SOURCE OF OXYGEN, AND CONTACT CUSTOMER SERVICE. 12. DO NOT USE CLEANING AGENTS OTHER THAN THOSE SPECIFIED IN THIS MANUAL. ALLOW THE CLEANING SOLUTION TO DRY FROM THE CLEANED SURFACE BEFORE USE.
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PRECAUTION: 17. ALWAYS OPERATE DEVICE AT THE SETTING PRESCRIBED BY A CLINICIAN. DO NOT ALTER THE SETTING UNLESS PRESCRIBED BY A CLINICIAN. 18. THIS DEVICE IS DESIGNED FOR USE BY ONE PATIENT AT A TIME. 19. THIS DEVICE MAY NOT REACH SPECIFIED OXYGEN CONCENTRATION PURITY UNTIL IT HAS BEEN IN USE FOR UP TO 10 MINUTES. 20. ALWAYS FOLLOW THE MAINTENANCE SCHEDULE AS SPECIFIED IN “ROUTINE MAINTENANCE” (PAGE 13). 21. IF THIS DEVICE INDICATES AN ABNORMAL CONDITION, SEE “TROUBLESHOOTING” (PAGE 20). 22. REMOVE BATTERY IF THIS DEVICE IS NOT GOING TO BE USED FOR MORE THAN SEVEN DAYS. STORE BATTERY IN A COOL, DRY PLACE. 23. ALWAYS FOLLOW CANNULA MANUFACTURER’S INSTRUCTIONS FOR PROPER USE. 24. ALWAYS TURN OFF THIS DEVICE WHEN NOT IN USE. 25. DO NOT USE THIS DEVICE WHILE SLEEPING UNLESS UNDER THE SUPERVISION OF A CLINICIAN. 26. DO NOT PLACE OBJECTS ON TOP OF THIS DEVICE. 27. THIS DEVICE IS RATED IPX2. DO NOT USE IN DUSTY CONDITIONS. 28. USE CAUTION WHEN TOUCHING THIS DEVICE IN HIGH AMBIENT TEMPERATURES. 29. CHECK THAT THIS DEVICE OPERATES ON BATTERY AFTER DISCONNECTING FROM THE POWER SOURCE. 30. ONLY CHARGE BATTERY IN THIS DEVICE OR IN AN APPROVED CHARGER. (SEE APPROVED ACCESSORIES GUIDE.) IMPORTANT: 1. If an extension cord is necessary, use a UL listed 15 amp or higher cord.
Contents Classification .................. iii Explanation of Packaging and Labeling Symbols ......... iv Introduction .................. vi Manual Version ................ vi General Information .............. vi Typographical Conventions ............ vi Indications for Use ................ vii Intended Use ................. vii Contraindications ................vii Warnings and Precautions ..............viii Warnings Overview ..............viii Precautions Overview ..............viii Before You Get Started ................. 1 Power Supply .................. 1 Charging the Battery .............. 2 Features and Controls ................ 4 Accessories .................. 6 Carrying Case ................ 6 Pull Cart ................... 7 Operating the Portable Oxygen Concentrator ........ 9 Connecting Nasal Cannula .............. 9 Turning On .................. 1 0 Adjusting Setting ................10 Responding to Alarms ..............11 Turning Off ..................11...
Before You Get Started A lways inspect the device and its accessories for any sign of damage before using. Note: While box or packaging may exhibit some damage, e.g., tears or dents, the device may still be in a usable condition. If the device or any accessory shows any sign of damage, contact your care provider. Before you get started, check to make sure you have the following: • Concentrator • Battery • Carrying case • AC/DC power supply See Approved Accessories Guide for more information. WARNING: DO NOT USE A PORTABLE OXYGEN CONCENTRATOR OR ANY ACCESSORY THAT SHOWS ANY SIGN OF DAMAGE.
Charging the Battery PRECAUTION: ONLY CHARGE BATTERY IN THIS DEVICE OR IN AN APPROVED CHARGER. (SEE APPROVED ACCESSORIES GUIDE.) Prior to using the Portable Oxygen Concentrator for the first time, install the battery as shown in Figure 1. The battery will latch when fully seated. Figure 1. Connect the AC power supply (consult Approved Accessories Guide) by plugging the round connector into the receptacle on the side of the concen- trator. See Figure 2. Plug the other end of the AC power supply into a power outlet. Always use caution when inserting the power supply to a wall outlet. Charger requirements are universal to support a wide variety of international markets, so it can be plugged into an outlet with 100-240V AC, 50-60 Hz. Allow the battery to charge for a minimum of three hours before use. Once the battery is completely charged, the device can run on battery for approxi- mately 2-3 hours at a setting of 2.0. Note: Battery run time may vary based on breathing rate, age of battery, and environmental conditions.
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Figure 2. Note: Ensure power status icon (see Figure 6, page 5) indicates power is connected. If not, check that cord is plugged in completely. (See “Troubleshooting” on page 20 for more information.) To maximize battery life and run time, use while connected to a power source whenever possible. The internal battery will automatically charge whenever the concentrator is connected to a power source. The LCD display will indicate whether the device is operating on battery or external AC power. The fully charged battery will retain some level of charge for up to seven days in this device when not in use. Note: Battery damage may result if the concentrator’s battery is allowed to discharge completely.
Features and Controls Figure 3. Power key – turns device on or off Display percent Display screen battery charge Alarm mute key – temporarily silences audible alarms or shows Red LED – indicates the last highest priority alarm a warning of danger and/or a need for Green LED –...
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Figure 5. Battery Input filter Air intake Compressor filter Setting Power status (battery) Setting Power status (external) Figure 6. DL-00096 Rev. 8...
ACCESSORIES A variety of accessories can enhance the portability and use of the Portable Oxygen Concentrator. In addition to the device, the package contains accessories to get started and instructions for use. Refer to the Approved Accessories Guide for the complete list of available accessories. Only use a nasal cannula with the following specifications: • 7’ (2.1 m) long • High flow • Three-fluted • Crush-resistant • Large internal diameter bore • Straight non-tapered tips • Suitable for up to 10 lpm Note: Recommended model is Salter Labs 1600 HF cannula. PRECAUTION: ONLY USE APPROVED ACCESSORIES WITH THIS DEVICE. REFER TO THE APPROVED ACCESSORIES GUIDE FOR A COMPLETE LIST OF ACCESSORIES AND CANNULA APPROVED FOR USE WITH THIS DEVICE. USING UNAPPROVED ACCESSORIES OR CANNULA MAY IMPAIR THE PERFORMANCE OF THIS DEVICE. Contact your distributor for updated information and accessories or if additional, optional, or replacement accessories are needed. Carrying Case To reduce the risk of electric shock, always use the Portable Oxygen Concentrator with a carrying case (which also further reduces the device noise during operation). Insert the device in the case such that the display screen is...
Figure 7. Pull Cart When using the Portable Oxygen Concentrator with a pull cart, attach and secure the concentrator with the straps as shown in Figure 8. The handle can be pulled out and adjusted for comfort. Note: It is recommended that patients use the pull cart to transport the device whenever possible. Figure 8. DL-00096 Rev. 8...
Operating the Portable Oxygen Concentrator IMPORTANT: Read “Warnings and Precautions” (page viii) before using this device. The Portable Oxygen Concentrator is designed for ease of use, with all functions accessed through just a few keys on the control panel. The Portable Oxygen Concentrator should be carried in its carrying case, placed on a cart, or used while laying on a table or upright on the floor. The patient should be within 7’ of this device during use. Note: Except during startup and shutdown sequences, the backlight on the display screen will remain off. Pressing any key will turn the backlight “on” briefly. The backlight will also remain activated during an un-muted alarm condition.
To connect the cannula to the patient, position the cannula tips in patient’s nostrils and pass tubing over both ears and under chin. Follow manufacturer’s instructions. Slide adapter up tubing to adjust for comfort and fit. Once the cannula is secured, breathe normally through the nose. The Portable Oxygen Concentrator will detect a breath and deliver the oxygen during inhalation. Note: Improper cannula placement may result in the Portable Oxygen Concentrator being unable to detect all respiratory efforts of the patient. Ensure cannula is connected securely and it has been fully inserted. PRECAUTION: PATIENTS WITH A FAST BREATHING RATE REQUIRING A HIGHER OXYGEN SETTING MAY REQUIRE MORE OXYGEN THAN THIS DEVICE CAN PRODUCE. THIS DEVICE MAY NOT BE APPROPRIATE IN THAT CASE.
Figure 11. Concentrator running on external power. RESPONDING TO ALARMS PRECAUTION: IF YOU ARE UNABLE TO HEAR OR SEE ALARMS, DO NOT HAVE NORMAL TACTILE SENSITIVITY, OR CANNOT COMMUNICATE DISCOMFORT, CONSULT CLINICIAN BEFORE USING THIS DEVICE. Pressing the alarm mute key at any time will silence the buzzer. The length of the mute period depends on the severity of the alarm. (See “Alarm Indicators” on page 16.) During this mute period, the mute LED will remain illuminated, indicating the alarm buzzer is muted. Push the mute key again to unmute alarms. Pressing the mute key when there is no active alarm will mute any future medium or low priority alarms for eight hours. See “Troubleshooting” (page 20) for additional information on alarms. TURNING OFF PRECAUTION: ALWAYS TURN OFF THIS DEVICE WHEN NOT IN USE. To turn the Portable Oxygen Concentrator off, press and hold the power key. The device will chirp and the screen will display a shutdown message “Shutting off” for approximately five seconds, then go into low-power mode. Note: Do not disconnect the AC power supply and remove the battery at the same time while the unit is running.
Maintenance and Cleaning VERIFYING THE ALARM SYSTEM At startup, the LEDs should light up and buzzer should sound to verify operation. BATTERY CARE Avoid letting battery deplete; operate device when connected to AC power whenever possible to help keep battery charged. Disconnect battery if the device will not be used for more than seven days, and store the battery in a cool, dry place. Dispose of battery according to local regulations or contact your distributor. ENVIRONMENT/STORAGE The Portable Oxygen Concentrator can operate in the following conditions: • 41°F to 95°F (5°C to 35°C) • 5% to 93% ± 2% relative humidity (non-condensing) • Altitudes between 0’ to 8,000’ above sea level (0 km to 2.4 km) When not in use, the Portable Oxygen Concentrator should be stored in a clean, dry environment between -4°F and 140°F (-20°C and 60°C). Note: The Portable Oxygen Concentrator can be safely stored up to 15,000’ (4,572 m) above sea level. WARNING: THIS DEVICE IS FOR CONTINUOUS OPERATION AT TEMPERATURES OF 95°F (35°C) DOWN TO 41°F (5°C), AND SHORT-TIME OPERATION...
ROUTINE MAINTENANCE WARNING: DO NOT USE LUBRICANTS ON THIS DEVICE OR ANY OF ITS ACCESSORIES. PRECAUTION: REPLACE THE CANNULA ON A REGULAR BASIS. CHECK WITH YOUR DISTRIBUTOR OR CLINICIAN TO DETERMINE HOW OFTEN THE CANNULA SHOULD BE REPLACED. Device will indicate with an alarm when a filter or device needs to be cleaned or changed. (Also, see “Troubleshooting” on page 20.) Cleaning and Changing Filters Filters in the Portable Oxygen Concentrator should be periodically washed or replaced as indicated by messages on the display screen.
PATIENT FILTER The patient filter is designed to trap airborne particulates. If the device indicates the patient filter should be replaced, contact your distributor for replacement filter. Replace as shown in Figure 12. Figure 12. COMPRESSOR FILTER The compressor filter is designed to trap airborne particulates. If the device indicates the compressor filter should be replaced, contact your distributor for replacement filter. Replace as shown in Figure 13. Figure 13. DL-00096 Rev. 8...
EXTERIOR CLEANING WARNING: DO NOT SUBMERGE THIS DEVICE IN LIQUID. DO NOT EXPOSE TO WATER OR PRECIPITATION. DO NOT EXPOSE TO DUSTY CONDITIONS. PRECAUTION: DO NOT USE CLEANING AGENTS OTHER THAN THOSE SPECIFIED IN THIS MANUAL. ALLOW THE CLEANING SOLUTION TO DRY FROM THE CLEANED SURFACE BEFORE USE.
Alarm Indicators If the Portable Oxygen Concentrator detects an alarm condition, it will indi- cate the alarm visually and audibly within 10 seconds. There are four levels of alarms: critical high priority, high priority, medium priority, and low priority. Each is indicated differently by the backlit display; green, yellow, and red LEDs; and buzzer, as indicated below. In each case, the alarm message and power status will override the current display. Note: All alarm conditions and parameters are factory preset; conditions and parameters cannot be changed or adjusted by the user. Alarm Status Audible Tone Visual Indicator Mute Time Critical high Ten beeps per burst, burst Solid red LED 20 minutes priority...
High Priority Alarms Note: These alarms will allow the Portable Oxygen Concentrator to continue operating. Alarm Message Description Action Check Vents Device is unable to maintain Be sure air inlet/outlet oxygen purity. has not been blocked. If alarm persists, contact your distributor. Low Battery Estimated battery life less Charge the battery pack than 17 minutes. by plugging in to power supply. Note: The message will be automatically cleared when plugged in to power supply.
Low Priority Alarms Alarm Message Description Action Replace C-filtr Compressor filter needs Replace filter. Press and replacement. hold mute key for more than 4 seconds to reset the hour counter. Replace P-filtr Patient filter needs Replace filter. Press and replacement. hold mute key for more than 4 seconds to reset the hour counter. Wash I-filtr Input filter needs to be Wash input filter. Press cleaned. and hold mute key for more than 4 seconds to reset the hour counter. Main battery has exceeded Replace batt Contact your distributor...
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Other Messages, continued Message Description Action Battery low Estimated battery life less Charge the battery pack than 17 minutes. The unit by plugging in to power will also generate a high supply. priority alarm as described Note: The message will be above. automatically cleared when plugged in to power supply. Fully charged Displayed as the battery No action is required.
Troubleshooting Problem Possible Cause Troubleshooting System becomes • S ystem may be • C heck that the system inoperative disconnected from the is connected securely power source. to the power source. • S ystem may be turned • E nsure the system is off. powered on. • C ritical high priority alarm • E xamine the system has occurred. for damage or expo- sure to liquids. • I f problem persists, contact your distribu- tor.
Appendix 1: Technical Description Size: 7.6” W x 5.6” D x 11.9” H (192 mm W x 142 mm D x 302 mm H) Unit weight: Less than 10 lbs (without carrying case or cart) Power requirements: 100-240V AC (± 10%), 50-60 Hz; battery power 18V DC, 6.7 amps; DC adap- tor, 18V DC, 6.7 amps (Note: See Approved Accessories Guide for model and part number of AC power supply.) Purity: 87% - 96% (22°C ± 3°C, 14.29 psia ± 0.04 or 739 mmHg at 40% ± 15% relative humidity) at all flow rates Setting: User adjustable 1.0 to 5.0 (with 0.5 increments) (min. 1.0; max. 5.0) Setting indicator: LCD display Maximum oxygen discharge pressure: 17 psi at setting of 5.0 Humidity range: 5% to 93% ± 2% non-condensing Operating altitude: 0’ to 8,000’ relative to sea level (0 km to 2.4 km) Sound pressure level (measured 1 m from edge of chassis): Less than 47 dB(A) average...
Appendix 2: Technical Information ELECTROMAGNETIC COMPATIBILITY (EMC) INFORMATION Medical electrical equipment requires special precautions regarding electromagnetic compatibility (EMC). Portable and mobile radio frequency (RF) communications equipment can affect devices such as the Portable Oxygen Concentrator. As such, the device should not be used adjacent to other equipment. If this is not practical, then observe the device to make sure it is operating properly at all times. Guidance and manufacturer’s declaration: electromagnetic emissions The Portable Oxygen Concentrator is intended for use in the electromagnetic environment specified below. The customer or the user of the concentrator should assure that it is used in such an environment. Emissions test Compliance Electromagnetic environment/guidance RF emissions Group 1 The Portable Oxygen Concentrator uses CISPR 11 RF energy only for its internal function. Therefore, its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment.
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Guidance and manufacturer’s declaration: electromagnetic immunity The Portable Oxygen Concentrator is intended for use in the electromagnetic environment specified below. The customer or the user of the concentrator should assure that it is used in such an environment. Immunity test IEC 60601 test Compliance Electromagnetic level level environment/guidance Electrostatic ± 6kV contact ± 15kV contact Floors should be wood, discharge (ESD) ± 8kV air ± 8kV air concrete, or ceramic tile. IEC 61000-4-2 If floors are covered with synthetic material, the relative humidity should be at least 30%. Electric fast ± 2kV for ± 2kV for Mains power quality transient/burst power supply power supply should be that of a typical IEC 61000-4-4...
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Immunity test IEC 60601 test Compliance Electromagnetic level level environment/guidance Voltage dips, short < 5% U < 5% U Mains power quality should interruptions, and (>95% dip in U (>95% dip in U be that of a typical voltage variations for 0.5 cycle for 0.5 cycle commercial or hospital on power supply environment. If the user 40% U 40% U input lines of the Portable Oxygen (60% dip in U (60% dip in U IEC 61000-4-11 Concentrator required for 5 cycles...
Note: These guidelines may not apply in all situations. Electromagnetic propagation is affected by the absorption and reflection from structures, objects, and people. Trademarks All trademarks are the property of their respective owners. Disclaimer The information in this document has been carefully examined and is believed to be reliable. Furthermore, Oxus reserves the right to make changes to any products herein to improve readability, function, or design. Oxus does not assume any liability arising out of the application or use of any product or cir- cuit described herein; neither does it cover any license under its patent rights nor the rights of others. DL-00096 Rev. 8...
Airline Travel Guidelines When traveling by air, it is recommended the guidelines listed below be followed: 1. The patient must be capable of seeing the alarm indicator lights, hearing the various warning alarms, and taking the appropriate actions should the unit fail to detect the user’s breathing or a general malfunction occurs. If the patient is not capable of the above requirement, they must be traveling with someone who is capable of performing those functions for the user. 2. Person using the Portable Oxygen Concentrator (POC) must not be seated in an aisle, normal exit row, or emergency exit so as not to restrict access to the aisle by other passengers. Patients should stow POC while in use, underneath seat, so that it does not interfere with the movement of other passengers. If patients are not required to use oxygen during takeoff, landing, or movement on the surface, they must stow the POC according to airline regulations (underneath seat or in overhead cabin). 3. Patient is responsible to carry sufficient amount of batteries to last for the entire trip, including layovers and/or possible flight delays. 4. Batteries, not being used or extra, must be stowed in their protective cover or/and placed inside the carrying case or placed inside an approved carry-on baggage, packaged to prevent short circuits and protected from physical damage. 5. Patient must obtain a signed, licensed clinician statement that medical oxygen is necessary for the duration of the flight and the maximum setting allowed onboard an aircraft. 6. The patient must inform the aircraft operator and its crew that the POC may be used onboard the aircraft. 7. In the event of an alarm, the POC must be turned off or alarms muted. 8. Only oxygen approved lotions or salves may be used by the patient. 9. The patient must operate the POC with battery power only (do not use the car charger) while onboard the aircraft. The A/C power cord and car charger options are not approved for onboard aircraft use.
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