BPAP Series User Manual V1.0
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2. Warning, Caution and Important Tip
WARNING!
Indicate the possibility of injury to the user or operator.
CAUTION!
Indicate the possibility of damage to the device.
IMPORTANT TIP!
Place emphasis on an operating characteristic.
Warnings, Cautions, and Important Tips appear throughout this manual as they apply.
3. Intended Use
The G3 B20A / B25S / B25A / B25VT / B30VT BPAP System is a Bi-level PAP (Bi-level Positive
Airway Pressure) device, which is intended to provide non-invasive ventilation for patients
with Obstructive Sleep Apnea (OSA) and Respiratory Insufficiency. These devices are
intended for adult patients by prescription in the home or hospital/institutional environment.
The G3 B30SV BPAP System is a Bi-level PAP (Bi-level Positive Airway Pressure) device,
which is intended to provide non-invasive ventilation for patients with Obstructive Sleep
Apnea (OSA), Central Sleep Apnea (CSA), Mixed Sleep Apnea (MSA), and periodic breathing.
This device is intended for adult patients by prescription in the home or hospital/institutional
environment.
The G3 LAB BPAP System is a Bi-level PAP (Bi-level Positive Airway Pressure) device, which is
intended to provide non-invasive ventilation treatment and titration for patients with
Obstructive Sleep Apnea (OSA), Central Sleep Apnea (CSA), Mixed Sleep Apnea (MSA),
periodic breathing and Respiratory Insufficiency. This device is intended for adult patients by
prescription in a clinical environment.
The optional SpO
2
module used with the G3 BPAP Series together is indicated for monitoring
patients’ SpO
2
and Pulse Rate auxiliarily.
WARNINGS!
• This device is intended for adult use only.
• This device is not intended for life support.
• The instructions in this manual are not intended to supersede established medical
protocols.
• To ensure that you receive the safe, effective therapy prescribed for you, use only BMC
accessories.
• Do not bring the device or accessories into a Magnetic Resonance (MR) environment as it
may cause unacceptable risk to the patient or damage to the device or MR medical devices.
The device and accessories have not been evaluated for safety in an MR environment.
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