What to do if my Feellife Air Kids Respiratory Product does not work when I turn it on?
If your Feellife Respiratory Product isn't working, ensure it has enough power by checking if the blue and green indicator is always on. If so, recharge the device. Also, verify that the medication cup has been properly filled.
Why does my Feellife Respiratory Product have low volume?
There are several reasons for low volume in your Feellife Respiratory Product: 1. Check that the medication cup is filled with the correct water-soluble, non-corrosive medication. 2. Ensure that the liquid amount is not excessive. 3. The spray mesh might be blocked. Try dropping 2-3 drops of white vinegar into the medication cup with 3-6ml of water, then fully nebulize. Afterward, clean the medication cup for disinfection before the next use.
General| Brand | Feellife |
|---|---|
| Model | Air Kids |
| Category | Respiratory Product |
| Language | English |
Identifies the product as a Portable Mesh Nebulizer.
Specifies the model number as Air Kids.
Explains how the mesh nebulizer atomizes liquid medication.
Defines the intended use and suitable users for the device.
Lists technical details like power supply, nebulization rate, etc.
Specifies the noise level of the nebulizer as 50dB.
Provides the physical dimensions and weight of the nebulizer.
Details the temperature, humidity, and pressure for operation.
Specifies conditions for storing and delivering the device.
The part responsible for atomizing the medication.
The cover for the medication cup.
The container for holding the liquid medication.
Controls the power state of the device.
The primary body of the nebulizer.
Port for connecting the charger to the device.
Accessory for inhalation for adult users.
Accessory for inhalation for child users.
Accessory for direct inhalation.
Instructions for charging the device's rechargeable battery.
Notes on battery replacement, only by manufacturer.
Recommendation to charge monthly during storage.
Specifies incompatible battery types.
Instruction to charge for 30 minutes before first use.
Guidance on maximizing battery service life.
Important warnings regarding battery disposal, repair, and handling.
Explanation of indicator lights and device modes.
Steps for operating the nebulizer for atomization.
Describes three methods of inhalation: direct, mask, and mouthpiece.
Steps for disassembling the nebulizer after use.
Detailed steps for cleaning the nebulizer components.
Caution against washing the main unit with water.
Instruction to use sterile gauze for drying.
Warning against placing masks in hot water.
Procedures for disinfecting components using hydrogen peroxide or ethanol.
Steps for disinfecting with 3% hydrogen peroxide solution.
Steps for disinfecting with 75% medical ethanol.
Caution about disinfectant residue and mesh diaphragm care.
Instructions for drying the nebulizer components after cleaning.
Guidance on proper storage conditions and duration.
Specifies environment temperature, humidity, and pressure for storage.
Instructions for storing the device after use.
Instructions for maintaining the device during normal operation.
Specifies environment and power requirements for operation.
General guidelines for device maintenance and care.
Guidance on seeking solutions for operational issues.
Instructions for drying and storing parts after use.
Warning about environmental factors affecting performance.
Instruction to contact company if the device malfunctions.
Lists conditions or substances not suitable for use with the nebulizer.
General advice, warnings, and recommendations for use.
Instruction to check accessory integrity before use.
Information on the disposable nature and reuse limit of the nozzle.
Advice to ensure sufficient liquid for mesh contact.
Prohibition of submerging or using in bathrooms.
Warning against use near flammable gases or oxygen.
Guidance on operating in controlled electromagnetic environments.
Caution against use in high temperatures due to fire risk.
Advice to keep device away from strong vibrations or impact.
Prohibition of liquids with esters, oils, or herbal extracts.
Caution against washing the whole unit, especially the USB connector.
Warning against using microwave ovens for drying.
Instruction to keep the device away from children and certain patients.
Recommendation to use qualified chargers.
Warning against touching the spray mesh with hands or sharp objects.
Note on the lack of moisture/dust protection and storage.
Instruction to stop use if device is dropped or damaged.
Warning against disassembling, repairing, or modifying the device.
Guidance on proper disposal according to local regulations.
Advice to consult a doctor for pre-existing conditions like diabetes.
Emphasis on consulting a doctor for medication and usage advice.
Instruction to stop use and seek medical help if feeling unwell.
Prohibition of volatile oils due to potential damage.
Recommendation for water-soluble medicines; warns against others.
Prohibition of oily medications.
States the device is not for respiration anesthesia or respirator systems.
Advise to check medication leaflets for contraindications.
Warning against liquids with viscosity over 5 to prevent mesh damage.
Recommendation to use only saline solution for medication.
Availability of maintenance information from the manufacturer.
Warning against spilling liquid to prevent electric shock or malfunction.
Troubleshooting steps for when the device does not power on.
Troubleshooting steps for low medication output.
Guidance on selecting suitable medications for nebulization.
Explanation for medication residue and stopping nebulization.
Instruction for special care for pediatric users.
Guidance on using individual consumable items like masks.
Instructions for disposing of rechargeable batteries.
Guidance for disposing of the device according to regulations.
Instruction to contact after-sales for warranty service.
Information on obtaining repair details and contacting the manufacturer.
Explanation of various symbols used in the manual and on the device.
General precautions related to device usage and safety.
States compliance with IEC60601-1-2 for electromagnetic compatibility.
User guidance on installing and using with EMC compatibility.
Warning about RF devices interfering with nebulizer performance.
Refers to appendix for guidance and manufacturer's declarations.
Details on electromagnetic interference and its effects on medical devices.
Requirement for medical devices not to interfere with other devices.
Explanation of IEC60601-1-2 standard for EMC.
States FEELLIFE devices conform to IEC60601-1-2.
Highlights special precautions to be observed for EMC.
Details emissions characteristics for residential environments.
Warning about using unauthorized accessories and cables.
Impact of using non-specified replacement parts on emissions/immunity.
Warning against using device adjacent to or stacked with other equipment.
Specifies minimum separation distance from RF equipment.
Warning about mobile devices generating strong fields near the unit.
Guidance for electromagnetic immunity based on environmental factors.
Details immunity test levels and environmental guidance.
Guidance on separation distances for RF equipment.
Table showing separation distances based on transmitter power and frequency.
Precautions for EMC compliance and potential interference.
Confirms conformance to EN60601-1-2:2015 standard.
Advice to avoid strong electromagnetic interference from RF devices.
Warnings regarding equipment stacking and component replacement.
Warning against stacking equipment without verification.
Impact of spare parts on emissions and immunity.
Details warranty period, exclusions, and service procedures.
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