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Summary of Contents for Pari LC SPRINT SPA
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Page 2: Table Of Contents
Instructions for use Information as of: December 2014. All rights reserved. Technical and design changes and printing errors reserved. Principle shown in illustrations. 1 IMPORTANT INFORMATION 1.1 General ......................1.2 Information about the instructions for use ............1.3 Structure of safety instructions ............... -
Page 3: Important Information
1 IMPORTANT INFORMATION 1.1 General Please read these instructions for use carefully and completely. Do not discard, so you can consult them at a later date. If you fail to comply with the instructions for use, injury or damage to the device cannot be ruled out. If symptoms persist or if your condition worsens, discontinue the application and contact your doctor immediately. -
Page 4: Hygiene
To find out which components are included in your pack, refer to the following table. Check that all components of your PARI product are contained in your package. If anything is missing, please notify the dealer from whom you purchased the PARI product immediately. -
Page 5: Intended Purpose
5. Child mask soft 6. Connection Tubing(f/f) 2.2 Intended purpose The nebuliser PARI LC SPRINT SPA is a medication nebuliser that is designed to be used in conjunction with a compressor for inhalation therapy of the lower and/or upper airways. -
Page 6: Operating Life
2.7 Operating life Replace the nebuliser after a year at the latest as changes can occur in the material of the nebuliser over time. This might impair the effectiveness of the treatment. 3 INHALATION 3.1 Assembling the nebuliser CAUTION Check all nebuliser components and the accessories before each use. Replace any broken, misshapen or seriously discoloured parts. -
Page 7: Filling With Medication
Using with a mouthpiece • Fit the mouthpiece onto the nebuliser. Using with a child mask Attach the child mask to the nebuliser. • When using a mask, make sure that the expiratory valve plate is pressed out so you can exhale freely during an inhalation session. 3.2 Filling with medication NOTICE Take care to ensure that the cap only moves in the direction allowed by the... -
Page 8: Performing The Inhalation
page 13]. If the nebuliser contains too little or too much medication, nebulisation, and thus also the treatment, will be greatly impaired. • Close the nebuliser cap. Make sure that the cap snaps into place. If you are to inhale several medications one after the other in one application, rinse out the nebuliser with tap water between inhalations. -
Page 9: Cleaning And Disinfection At Home
• Replace the nebuliser in the holder as soon as you have finished inhaling. • Switch the compressor off. 4 CLEANING AND DISINFECTION AT HOME The nebuliser and the accessories used must be cleaned thoroughly after each application and disinfected at least once a day. The connection tubing cannot be cleaned or disinfected. -
Page 10: Disinfection
• Rinse all parts thoroughly in running water. • You can remove excess water more quickly by shaking all parts. 4.4 Disinfection After cleaning, disinfect the dismantled nebuliser and accessories used (except for the connection tubing). Effective disinfection is only possible if the nebuliser has been cleaned. - Page 11 Inadequate disinfection encourages the growth of bacteria and thus increases the risk of infection. Thorough disinfection has not been completed until the disinfector automatically switches itself off, or the minimum disinfection time specified in the instructions for use of the disinfector has elapsed.
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Page 12: Visual Inspection
unless both the specified minimum disinfection time and the required power output of the microwave are observed. The disinfector must also be perfectly clean. Check regularly that the microwave and the disinfector are functioning perfectly. Use only water for disinfection, never use chemicals. 4.5 Visual inspection Inspect all product components after each cleaning and disinfection. -
Page 13: Explanation Of Symbols
5.3 Explanation of symbols The following symbols can be found on the product and/or the packaging: Manufacturer The product satisfies the basic requirements as set forth in Appendix I of Directive 93/42/EEC concerning medical devices. Please follow the instructions for use. Order no.
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