What to do if my GCE Medical Equipment system becomes inoperative?
If your GCE Medical Equipment system becomes inoperative, first check that the system is securely connected to the power source and powered on. If the problem persists, examine the system for damage or exposure to liquids. If none of these actions restore the system's functionality, contact your distributor.
Why is my GCE Zen-O lite RS-00600 battery not charging?
If your GCE Medical Equipment battery isn't charging, ensure the power is correctly connected and that the round receptacles are secure in the unit. Also, verify the battery is fully seated and the battery cover is secure. If the problem persists, contact your distributor.
What to do if the GCE Medical Equipment system becomes inoperative?
If the GCE Medical Equipment system becomes inoperative, first, check that the system is securely connected to the power source. Next, ensure the system is powered on. Also, examine the system for damage or exposure to liquids, as a critical high-priority alarm may have occurred.
Provides information for users of the Zen-O lite™ Portable Oxygen Concentrator.
Device classification regarding electric shock, fire, and mechanical hazards.
Explains symbols used for warnings, cautions, and important information.
Details critical safety warnings and potential hazards associated with the device.
Outlines necessary precautions and special care for safe and effective device use.
Provides crucial details regarding extension cords, inhalation, and daily usage.
Illustrates and labels the various components and indicators of the device.
Lists approved power supplies, adapters, and accessories for safe device operation.
Details on the internal rechargeable battery, charging, and battery status.
Specifies approved nasal cannula types and their proper usage guidelines.
Step-by-step guide on how to connect the nasal cannula to the device and patient.
Instructions for powering on the device, including startup sequence and LED indicators.
Procedure for selecting the display language on the device.
Explains how to adjust the oxygen delivery setting and understand modes like Auto Mode.
Details on the Eco Mode for extended battery duration and how to switch between modes.
How to use the battery button to check battery status and charge cycles.
Guidance on understanding and responding to various alarm conditions and mute functions.
Procedure for safely powering down the device.
Covers required labeling, consultation with healthcare providers, and battery determination.
Information on carry-on baggage, checked baggage, and placement/stowage on aircraft.
Details on security screening considerations for respiratory devices.
Instructions on how to enable or disable Airplane Mode for air travel.
Details critical, high, medium, and low priority alarms, their messages, and required actions.
Identifies common causes for the system becoming inoperative and provides solutions.
Lists possible causes for the battery not charging and troubleshooting steps.
Guidelines for regular upkeep, including cannula replacement and device checks.
Procedures for cleaning and disinfecting the device exterior and accessories.
Information on the expected service life of the device and sieve modules.
Details the service connector and its usage for service purposes only.
Instructions on how to handle device repair, emphasizing contacting a provider.
Step-by-step guide for replacing the sieve modules, including leak testing.
Guidance on proper disposal of the device and battery according to regulations.
States that all trademarks are property of their respective owners.
Provides information on the document's content, liability, and potential changes.
Details device dimensions, weight, power, electrical protection, and environmental ranges.
Covers purity, settings, sensitivity, pressure, altitude, sound, and safety ratings.
Table showing bolus size in ml/breath for different settings and breath rates.
Table showing bolus size in ml/breath for different settings and breath rates in Eco Mode.
Guidance on electromagnetic emissions and manufacturer's declaration for the device.
Guidance on electromagnetic immunity and manufacturer's declaration for the device.
Recommends minimum separation distances for RF communications equipment.
FCC compliance statement for model RS-00600C, including interference and exposure limits.
Information on EU RED Article 10(10) restrictions for RS-00600C model.
Details on RF exposure limits and Specific Absorption Rate (SAR) for the device.
Explains symbols for instructions, safety, warnings, and handling.
Defines symbols for serial numbers, compliance, and restrictions.
Explains symbols related to smoking, WEEE, battery disposal, and homecare use.
General| Brand | GCE |
|---|---|
| Model | Zen-O lite RS-00600 |
| Category | Medical Equipment |
| Language | English |
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