This innovative, trend-setting hip bag is the first of its kind for the oxygen user! A sturdy thermoformed belt provides padded comfort and stability to allow a greater sense of mobility without the fear of damaging the device.
Twin pockets provide space for carrying an extra battery plus a cell phone, wallet, keys, or other personal items. We proudly present the ultimate in hands-free mobility for the active oxygen user.
Order your Inogen One G4 Hip Bag today and enjoy your freedom!
Additional Accessories
Specifications apply to all new retail units sold after December 7th 2015.
1By submitting this information, I authorize Inogen to contact me, including by phone.
* Inogen One G4 weighs 3.3 pounds, height 7.8 inches, length 5.91 inches, width 2.68 inches (incl. double battery). Inogen One G5 weighs 5.7 pounds, height 9.03 inches, length 7.19 inches, width 3.26 inches (incl. double battery)
** Co-payments and deductibles may occur.
*** Specifications for rental units through insurance may vary.
**** Meets FAA Requirements. Check with your carrier for local regulations. Based on technical performance test data.
† Applicable for purchases only.
Please note that the health related information contained on this website is provided for general information purposes and is not intended to be a substitute for professional medical advice or for the care that patients receive from their healthcare professionals. For information about Inogen products you should consult the Instructions For Use (IFU). References to products, services, or health care providers on this website are not a recommendation or endorsement of products, services or providers. PLEASE CONSULT WITH YOUR DOCTOR, OR OTHER QUALIFIED HEALTHCARE PROFESSIONAL, BEFORE USING ANY PRODUCT REFERRED TO ON THIS WEBSITE.
The testimonials and opinions presented on our website are applicable to the individuals depicted. Results will vary and may not be representative of the experience of others.
‡ View Inogen's Limited Warranty Statement
Inogen One Portable Oxygen Concentrator
USES: The Inogen One Portable Oxygen Concentrator provides a high concentration of supplemental oxygen to patients requiring respiratory therapy on a
prescriptive basis. It may be used in home, institution, vehicle and various mobile environments. DO NOT USE IF: This device is not intended to be used in any
way other than described in the indications for use. Do not use in parallel or series with other oxygen concentrators or oxygen therapy devices. This device is to
be used as an oxygen supplement and is not intended to be life sustaining or life supporting. ONLY use this product if the patient is capable of spontaneous
breath, able to inhale and exhale without the use of a machine. The conserving, or pulse dose, oxygen delivery technique used by this device is contraindicated in
persons whose breathing during normal resting would be unable to trigger the device. Proper device triggering, set up and operation must be confirmed by an
experienced clinician or other respiratory professional. Not for pediatric use. Not for use by tracheotomized patients. WARNINGS: The device produces
enriched oxygen gas, which accelerates combustion. Do not allow smoking or open flames within 2m (6.56ft) of this device while in use. If you feel ill or
uncomfortable, or if the concentrator does not signal an oxygen pulse and you are unable to hear and/or feel the oxygen pulse, consult your equipment provider
and/or your physician immediately. If you are unable to communicate discomfort, you may require additional monitoring and or a distributed alarm system to
convey the information about the discomfort and or the medical urgency to your responsible caregiver to avoid harm. Use only spare parts recommended by
the manufacturer to ensure proper function and to avoid the risk of fire and burns. To avoid danger of choking or strangulation hazard, keep cords away from
children and pets. TALK TO YOUR HEALTH CARE PROVIDER: The oxygen flow setting must be determined and recorded for each patient individually by the
prescriber, including the configuration of the device, its parts and the accessories. It is the responsibility of the patient to periodically reassess the setting(s) of
the therapy for effectiveness. The proper placement and positioning of the prongs of the nasal cannula in the nose is critical for oxygen to be delivered.
Inogen At Home Stationary Oxygen Concentrator
USES: The Inogen At Home Oxygen Concentrator is used on a prescriptive basis by patients requiring supplemental oxygen. It supplies a high concentration of
oxygen and is used with a nasal cannula to channel oxygen from the concentrator to the patient. The Inogen At Home Oxygen Concentrator may be used in a
home or institution. DO NOT USE IF: This device is not intended to be used in any way other than described in the indications for use. This device is to be used as
an oxygen supplement and is not intended to be life sustaining or life supporting. ONLY use this product if the patient is capable of spontaneous breath, able to
inhale and exhale without the use of a machine. Not for pediatric use. Not for use by tracheotomized patients. WARNINGS: The device produces enriched oxygen
gas, which accelerates combustion. Do not use the device when smoking or near open flame, matches, petroleum, oil, grease, solvents, radiant heaters, aerosols,
etc. If you feel ill or uncomfortable, consult your equipment provider and/or your physician immediately. If you are unable to communicate discomfort, you may
require additional monitoring and or a distributed alarm system to convey the information about the discomfort and or the medical urgency to your responsible
caregiver to avoid harm. Use only spare parts recommended by the manufacturer to ensure proper function and to avoid the risk of fire and burns. To avoid
danger of choking or strangulation hazard, keep cords away from children and pets. TALK TO YOUR HEALTH CARE PROVIDER: The oxygen flow setting must be
determined and recorded for each patient individually by the prescriber, including the configuration of the device, its parts and the accessories. It is the
responsibility of the patient to periodically reassess the setting(s) of the therapy for effectiveness. The proper placement and positioning of the prongs of the
nasal cannula in the nose is critical for oxygen to be delivered.
Inogen TAV Tidal Assist Ventilator
USES: The Inogen Tidal Assist Ventilator (TAV), with accessories, is a volume assist ventilator intended to aid adult patients with respiratory insufficiency. It is
designed for patients who are capable of spontaneously breathing a minimum tidal volume of 3.5cc/kg of predicted body weight. The device is designed for
continuous applications such as patient ambulation, physical therapy, occupational therapy, respiratory therapy, and other rehabilitation efforts in an
institutional or home care environment. The device is intended for operation by trained personnel, patients or caregivers under the direction of a physician. DO
NOT USE IF: This device is not intended to be used in any way other than described in the indications for use. This device is not intended for patients who are
fully dependent on mechanical ventilation. ONLY use this product if the patient is capable of spontaneous breath, able to inhale and exhale without the use of a
machine. WARNINGS: This device may cause drying or irritation of the nasal passages. The use of the Tidal Assist ventilation system requires moderate patient
participation; therefore, you must be able to understand and comply with instructions. If you take strong sedatives or other medications that may inhibit mental
capacity, you should not use the system without proper medical supervision. Oxygen supports combustion. Oxygen should not be used while smoking or in the
presence of an open flame. Oxygen which has accumulated within in the device enclosure or tubing could pose a risk of fire. To avoid danger of choking or
strangulation hazard, keep cords away from children and pets. TALK TO YOUR HEALTH CARE PROVIDER: Expert clinical judgment should be exercised in the
appropriate use and selection of device settings for each individual patient. Inappropriate patient selection or selection of TAV settings may result in suboptimal
delivery of oxygen and/or breathing assistance to the patient. The oxygen flow setting must be determined and recorded for each patient individually by the
prescriber, including the configuration of the device, its parts and the accessories. It is the responsibility of the patient to periodically reassess the setting(s) of
the therapy for effectiveness. The proper placement and positioning of the prongs of the nasal cannula in the nose is critical for oxygen to be delivered.
G3, G4, G5, Inogen, Inogen At Home, Inogen One, and TAV are trademarks of Inogen, Inc. The usage of any Inogen, Inc. trademarks is strictly forbidden without the prior consent of Inogen, Inc. All other trademarks are trademarks of their respective owners or holders.
The Inogen One portable oxygen concentrators are available by Rx only. For safe and proper use of the Inogen One devices, please refer to https://www.inogen.com/support/inogen-manuals/
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