Compressor Nebulizer Model No.: 9R-021000 Please read the manual before use.
IMPORTANT SAFEGUARDS ........................................................................................... 1 1. INTRODUCTION ......................................................................................................... 3 2. PRODUCT DESCRIPTION........................................................................................ 4 3. OPERATION................................................................................................................ 5 4. CLEANING...............
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 with 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: 1. Always unplug this product immediately after using. 2. Do not use while bathing, showering, dish washing, or close to water sources of any kind. 3.
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.
English 1. Introduction 1.1 Intended Use The Mini-Plus Compressor Nebulizer System is intended to provide a source of compressed air for 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.
English 2. Product Description Compressor Main Unit 1. Power Switch 2. Filter Cap (disposable filter inside) 3. Air-Outlet Connector 4. Integrated Carrying Handle 5. Power Cord 6. Tubing Holder 7.
English 3. Operation NOTE - Before initial operation, 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 served to disconnect the device. 3.1 Daily Use Operation CAUTION - The Mini-Plus Compressor is designed for intermittent use only.
English 4. Cleaning 4.1 Compressor Outer Case Cleaning WARNING - Electric shock hazard. Do not remove outer case of this unit. All disassembly and maintenance of this unit must be done by a qualified service technician. Refer servicing to qualified service personnel. WARNING - This unit does not require oil. Do not attempt to lubricate any internal parts. WARNING - Unplug unit before cleaning. Do not submerge in water for cleaning. 1.
English 6. Maintenance 6.1 General Information 1. This unit is oil-less. Do Not Lubricate. 2. Risk of electric shock. Do not disassemble the main unit. 3. All maintenance must be performed by a qualified service personnel. 6.2 Filter Change NOTE - Change the filter once every month or when filter turns gray. 1. Open the filter cap. 2. Remove dirty filter with a small, pointed object. Discard the filter. 3. Replace with a clean filter. Additional filters should be purchased from your provider.
English 7. Troubleshooting If your Mini-Plus Compressor Nebulizer fails to function, consult the Troubleshooting guide below. If the problem persists, consult your equipment provider. Problem Device doesn’t operate. Cause and Solution • Check if plug is properly fit into an appropriate electrical outlet. • When device has been run continuously for over 30 minutes right before using, an auto shut down may activate by built-in thermal protector, cool down device for 30 minutes before next usage.
English 8. Specifications Electrical Rating (Note: Refer to the rating label on 120VAC,60Hz,1.2A the product) Operation Flow Rate ≧35 psi ≧5.5lpm Nebulization Rate 0.2~ 0.3 ml/min* Particle size 0.5 ~ 5 microns ( m)* Maximum Compressor Pressure μ Class II. BF equipment. Classification IPXO. No AP/APG protection. Applied part Mouthpiece or Nasal mask Dimensions (W x D x H) 14.0 Weight 1.6 kg / 3.5 lb Fuse T5A 250VAC for 120V system × 18.8 × 10.0 cm / 5.5” × 7.4” × 3.
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.
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.
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.
APEX MEDICAL S.L. Elcano 9, 6a 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.