Related Manuals for Apex Digital Mini-Plus
Summary of Contents for Apex Digital Mini-Plus
- Page 1 Compressor Nebulizer Model No 9R-021 series Please read the instruction manual before use.
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Page 2: Table Of Contents
IMPORTANT SAFEGUARDS ..........1 1. INTRODUCTION............... 6 2. PRODUCT DESCRIPTION ..........7 3. OPERATION ..............8 4. CLEANING ................ 9 5. STORAGE ................. 9 6. MAINTENANCE .............. 10 7. TROUBLESHOOTING ............ 10 8. SPECIFICATIONS ............11 9. EXPECTED SERVICE LIFE..........11 APPENDIX A: EMC INFORMATION ........ -
Page 3: Important Safeguards
English CAUTION - U.S. Federal Law restricts this device to sale by or on the order of a physician. This product has been tested and successfully approved to the following standards: EN 60601-1 EN 60601-1-2 0197 IMPORTANT SAFEGUARDS SAVE THESE INSTRUCTIONS READ ALL INSTRUCTIONS BEFORE USING DANGER - To reduce the risk of electrocution:... - Page 4 English NOTE, CAUTION, WARNING STATEMENTS AND SYMBOLS: NOTE Indicates information that user should pay special attention to. CAUTION Indicates correct operating or maintenance procedures in order to prevent damage to or destruction of the equipment or other property. WARNING Calls attention to a potential danger that requires correct procedures or practices in order to prevent personal injury.
- Page 5 English SYMBOLS – Manufacturer Authorized representative in the European community Off, disconnection from the mains On, connection to the mains ～ ～ ～ ～ Alternating current CAUTION should be used to highlight the fact that there are specific warnings or precautions associated with the device.
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Page 6: Introduction
English 1. Introduction 1.1 Intended Use The Mini Plus Compressor Nebulizer System is intended to provide a source of compressed aerosol therapy. It is used in conjunction with a jet (pneumatic) nebulizer to produce medicated aerosols for inhalation by pediatric and adult patients with respiratory symptoms. CAUTION Indications for therapy include asthma, chronic bronchitis, infection of the upper respiratory tract, chronic obstructive pulmonary disease and other... -
Page 7: Product Description
English 2. Product Description 1. Power Switch 2. Filter Cap (disposable filter inside) 3. Air-Outlet Connector 4. Integrated Carrying Handle 5. Power Cord 6. Tubing Holder 7. Cooling Air Openings... -
Page 8: Operation
English 3. Operation NOTE - Before first use, the nebulizer cup assembly should be cleaned following instructions described in the “Cleaning” section. WARNING - Before connecting the power cord, make sure the I/O (ON/OFF) switch is in the O (OFF) position. The plug is also used to disconnect the device. -
Page 9: Cleaning
English 3.2 Safety Overload NOTE - Do not exceed 30 minutes of continuous operation. 1. The motor of this device has a built-in thermal overload protector. Should the motor overheat, the protector will automatically shut off the motor. Should this occur, turn the I/O (ON/OFF) switch to the O (OFF) position and allow the motor to cool down for approximately 30 minutes before turning it on again. -
Page 10: Maintenance
English 6. Maintenance 6.1 General Information This unit is oil-less. Do Not Lubricate. Risk of electric shock. Do not disassemble the main unit. All maintenance must be performed by qualified service personnel. 6.2 Filter Change NOTE - Change the filter once every month or when filter turns gray. Please follow the instructions below as shown to the right. -
Page 11: Specifications
English 8. Specifications Electrical Rating 230VAC,60Hz,0.6A 230VAC,50Hz,0.6A (Note: Refers to the rating (for 230V system) (for 230V system) label on the product) Maximum Compressor ≧ 3 5 psi ≧ 3 5 psi Pressure 6 .0 lpm 5 .5 lpm Operating Flow Rate ≧... -
Page 12: Appendix A: Emc Information
English Appendix A: EMC Information Guidance and Manufacturer’s Declaration- Electromagnetic Emissions: This device is intended for use in the electromagnetic environment specified below. The user of this device should make sure it is used in such an environment. Emissions Test Compliance Electromagnetic Environment-Guidance The device uses RF energy only for its internal function. - Page 13 English Guidance and Manufacturer’s Declaration - Electromagnetic Immunity: This device is intended for use in the electromagnetic environment specified below. The user of this device should make sure it is used in such an environment. Immunity Test IEC60601 test level Compliance Electromagnetic Environment-Guidance Portable and mobile RF communications equipment should be used no closer to any part of this device, including cables, than...
- Page 14 English Recommended separation distances between portable and mobile RF communications equipment and this device: This device is intended for use in an electromagnetic environment in which radiated RF disturbances are controlled. The customer or the user of this device can help prevent electromagnetic interference by maintaining a minimum distance between portable and mobile RF communications equipment (transmitters) and this device as recommended below, according to the maximum output power of the communications equipment Separation distance according to frequency of transmitter m...
- Page 15 APEX MEDICAL S.L. Elcano 9, 6 planta 48008 Bilbao. Vizcaya. Spain APEX MEDICAL CORP. No.9, Min Sheng St., Tu-Cheng, New Taipei City, 23679, Taiwan Manufacturing Facility: Apex Medical (Kunshan) Corp. No. 1368, Zi Zhu Rd.,Kunshan Kai Fa Hi-Tech, Kunshan City, JiangSu Sheng, China www.apexbrand.com Print-2012/All rights reserved...
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