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Summary of Contents for Prolife PN MESH
- Page 1 NEBULIZER Prolife PN MESH Quick guide Instruction manual...
- Page 2 QUICK GUIDE...
- Page 3 max 6 ml 6 ml 6 ml 2 ml min 0.5 ml 2 ml 6 ml 2 ml 6 ml 2 ml QUICK GUIDE...
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Page 4: Maintenance
MAINTENANCE 6 ml 2 ml 6 ml 2 ml 100°С ~3 min QUICK GUIDE... -
Page 5: Table Of Contents
NEBULIZER PROLIFE PN MESH CONTENTS Introduction .............................6 List of symbols ............................6 3 Scope of application ..........................7 Complete set ............................9 5 Device description ..........................10 Basic specifications ..........................11 7 Safety instructions ..........................13 8 Before you start ............................14 9 Operating principles and procedures ....................15 10 Device cleaning .............................10... -
Page 6: Introduction
INTRODUCTION Dear Customer, thank you for choosing our products! Nebulizer Prolife PN Mesh is a medical device, this device has been designed using the advanced medical technologies in the treatment and prevention of respiratory tract diseases. Nebulizer Prolife PN Mesh is the most convenient portable and quiet device. -
Page 7: Scope Of Application
Serial number. SCOPE OF APPLICATION ENVIRONMENT OF US Nebulizer Prolife PN Mesh is designed for use in medical establishments, such as hospitals, clinics and medical offices, in home and other environments, including living rooms or outdoor sheltered areas. INTENDED USERS •... - Page 8 Users should also understand the operating principle of Nebulizer Prolife PN Mesh and read the instruction manual before using the device. The nebulizer is a medical device. Please follow your doctor’s prescriptions to choose the proper type, dosage and medication regimen.
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Page 9: Complete Set
COMPLETE SET The set includes the following components. If you find that any of the components are missing, please contact the retailer from whom you purchased the product. Protective Medication Inhalation Inhalation Main unit cover chamber mask S mask M Tip / Mouthpiece USB-С... -
Page 10: Device Description
DEVICE DESCRIPTION Decorative panel 8 ml Push button 2 ml (press to remove Terminal medication block chamber) Multifunction button (I / O button) Battery compartment Medication chamber USB-C port Connecting piece... -
Page 11: Basic Specifications
BASIC SPECIFICATIONS Category Nebulizer Model Prolife PN Mesh Spraying method Active Vibrating Mesh Technology Dimensions, mm 44 х 66 х 112 Weight, g (without batteries) ~ 90 Power source 3 V DC (АА 1,5 V alkaline battery х2); USB-Type С, 5 V DC 1 A (optional) Vibration frequency, kHz ~ 113... - Page 12 Nebulizer Prolife PN Mesh produces a high-frequency sound and automatically switches off if the medication does not get on the medication chamber membrane within 15 seconds (time varies for different types of solutions) or if the medication runs out.
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Page 13: Safety Instructions
SAFETY INSTRUCTIONS Read the instruction manual carefully before using the device to ensure its safe and proper operation. WARNINGS • Please follow your doctor’s prescriptions to choose the proper type, dosage and medi- cation regimen. • Do not fill the medication chamber with solutions not prescribed by your doctor. •... -
Page 14: Before You Start
• This device should not be used by physically, nervously or mentally disordered people (including children), or by the people who have insufficient experience and knowledge, unless they are supervised or instructed by the persons responsible for their safety. You should supervise the children and not allow them to play with the device, its compo- nents and original package. -
Page 15: Operating Principles And Procedures
OPERATING PRINCIPLES AND PROCEDURES «AA» batteries or 5V 1A power supply can be used for this product. HOW TO INSTALL BATTERIES Open the battery cover and install 2 «AA» alkaline batteries. 1. Open the battery cover. 2. Insert the batteries, observing the polarity, as shown in the picture. 3. Close the battery cover. - Page 16 HOW TO FILL THE CHAMBER WITH MEDICATION Remove the medication chamber from the main unit: 1. Take decorative panel away. 2. Press the «PUSH» button to remove the medication cham- ber from the main unit. 6 ml 3. Pull the medication chamber away. ATTENTION Please make sure you press the button before you start to remove the medication chamber.
- Page 17 Re-attach the medication chamber to the main unit: 1. Insert the medication chamber till it goes click. 2. Install the decorative panel. 3. Install the mask of a suitable size or the mouthpiece. ATTENTION • Make sure that the medication chamber is properly installed, as improper installation may cause the device malfunction.
- Page 18 3. Inhalation. Securely hold the nebulizer in your hand and start inhaling. Spray rate adjustment It can be difficult for children to breathe at an average spray rate, especially at the beginning of the treatment cycle. Breathing can also be complicated by illness. To make inhalation procedures more comfortable for the user, we have introduced the possibility to change the spray rate of the solution.
- Page 19 LED blinked 1 time: minimum spray rate is selected. LED blinked 2 times: average spray rate is selected. LED blinked 3 times: maximum spray rate is selected. minimum average maximum spray spray spray ATTENTION • If the device does not detect the medication in the chamber, it will automatically switch off. •...
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Page 20: Device Cleaning
Power off • The nebulizer switches automatically within 15 seconds 15 s. after the medication runs out. 6 ml • If you want to stop the inhala- 0 ml auto OFF tion procedure, press the I / O button to turn off the power. The power indicator will go out. - Page 21 • Rinse the medication chamber with distiller water after cleaning with citric acid solu- tion. To do this, fill the chamber with distilled water up to the level of 6 ml, close the lid and shake the chamber at least 5 times. Open the lid and remove water. Rinse the outer part of the membrane with distilled water to remove the citric acid solu- tion residue.
- Page 22 5. Wipe the main unit with a clean cloth. • Soak the cloth in water and gently wipe the main unit. Then wipe the unit dry using a new, clean, dry cloth. 6 ml WARNING Please clean the contacts on the main unit and medication chamber. This will ensure normal electrical conductivity and therefore normal spraying.
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Page 23: Troubleshooting
TROUBLESHOOTING In n case of problems with the device, please refer to the following table. Problem Possible causes Solution Extremely low spray rate Medication chamber is not Install the medication chamber securely installed properly Medication does not get on the Place the nebulizer at an angle membrane for more than 15 so that the medication gets on... - Page 24 Power indicator is on and the Medication chamber membrane Replace the medication chamber nebulizer does not work is damaged with a new one Medication chamber contacts are Clean the contacts from medica- contaminated with medication tion or water residues or water Nebulizer and medication cham- Clean the contacts ber contacts are contaminated...
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Page 25: Storage, Transportation And Operation Rules
STORAGE, TRANSPORTATION AND OPERATION REQUIREMENTS • The device should be stored within the temperature range from -20 ° С to +55 ° С with relativehumidity up to 93%. • The device should be transported within the temperature range from -20 ° С to +55 ° С with relative humidity up to 75%. -
Page 26: Certification
CERTIFICATION Changes or modifications not expressly approved by the party responsible for compliance could void the user’s authority to operate the equipment. Guidance and Manufacturer’s declaration – electromagnetic emissions The device is intended for use in the electromagnetic environment specified below. The customer or the user of the device should assure that it is used in such an environment Emissions test Compliance... - Page 27 Electrical fast ±2kV for power Not applicable Mains power quality should be that of a transient / burst supply lines typical commercial or hospital environment IEC 61000-4-4 ±1 kV for Input / output lines Surge 1kV line(s) to line(s) Not applicable Mains power quality should be that of a IEC 61000-4-5 typical commercial or hospital environment 2kV line(s) to earth...
- Page 28 Guidance and manufacturer’s declaration – electromagnetic immunity – for device that is not LIFE-SUPPORTING. Guidance and manufacturer’s declaration – electromagnetic immunity The device is intended for use in the electromagnetic environment specified below. The customer or the user of the device should assure that it is used in such an environment Immunity IEC 60601 Compliance...
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Page 29: Manufacturer's Warranty
b. Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V / m. Recommended separation distances between portable and mobile RF communications equipment and the device – for device that is not LIFE-SUPPORTING. Recommended separation distances between portable and mobile RF communications equip- ment and the device The device is intended for use in an electromagnetic environment in which radiated RF disturbanc- es are controlled. - Page 30 to consumables, constituent parts and components, such as: protective cover, batteries, tip / mouthpiece, carrying / storage case, USB-Type C cable, inhalation masks (S, M), package. Warranty and free maintenance service is not provided in case of: • violation of operating instructions; • damage caused by intentional or erroneous actions of the consumer due to improper or negligent handling;...
- Page 31 Manufacturer / Изготовитель: Shenzhen Combei Technology Co., Ltd., 11-5B, No. 105, Huanguan South Road, Dahe Community, Guanhu Street, Longhua District, Shenzhen, 518110 Guangdong, People's Republic of China / Китайская Народная Республика. Authorized Representative in the EU / Уполномоченный представитель в ЕС: MedNet EC-REP GmbH, Borkstrasse 10, 48163 Münster, Germany. 0123...
- Page 32 Prolife® is the registered trademark by Montex Swiss AG, Tramstrasse 16, CH–9442, Berneck, Switzerland...
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