Air Liquide Soffio Cube Instruction Manual Download Page 12

1. Fill the nebuliser with the inhalation solution as per your doctor’s instructions (Fig.B). Ensure 

that you do not exceed the maximum level.

2. Assemble the nebuliser and connect the mouthpiece or the nosepiece or the mask. (Fig.C). 

Ensure that all parts are complete.

3. Connect the nebuliser with the connecting tube (14) to the compressor (1) and plug the power 

cable (2) into the socket.

4. To turn on the device, push the ON/OFF switch (3) onto the position «I». Lean the mouthpiece 

between the lips or the nosepiece on the nostrils or lean the mask to the face over mouth 

and nose.

5. Sit in a relaxed position with the upper body upright. Breathe in and out calmly during the 

therapy. Do not lie down while inha¬ling. Stop inhalation if you feel unwell.

6. After completing the inhalation period recommended by your doctor, switch the ON/OFF switch 

(3) to position «O» to turn off the device and unplug it from the socket. 

7. Empty the remaining medication from the nebuliser and clean the device as described in the 

section «Cleaning, disinfecting and sterilizing».

 3 - CLEANING, DISINFECTING AND STERILIZING 

 

 

Always wash your hands well before cleaning and disinfecting the accessories. 

Do not expose the compressor to water or heat. 

Replace the connecting tube for each treatment with a new patient or in case of impurities.

  Unplug the device before cleaning.

Cleaning

The compressor unit (1) and the connecting tube (14) should be cleaned with a clean, moist cloth.

Clean all the nebuliser components and its accessories under warm tap water (max. 60°C) 

adding if necessary a small quantity of detergent following dosage and use limitations as 

provided by detergent manufacturer. Rinse thoroughly making sure that all deposits are washed 

away and leave to dry.

Disinfecting 

 

The compressor unit (1) can be disinfected with a clean cloth and some chemical disinfectant 

following dosage and use limitations as provided by disinfectant manufacturer.

All the accessories (except the connecting tube) can be disinfected with chemical disinfectants 

following dosage and use limitations as provided by disinfectant manufacturer. Disinfectants are 

usually available at pharmacies.

Steam sterilizing

The nebuliser and its accessories (except air hose and masks) can be heat steam sterilized 

up to 121 °C (20 min.) or 134 °C (7 min.). EN554/ISO11134.The sterilization packaging must 

conform to EN868/ISO11607 and be suitable for steam sterilization. After sterilization always let 

all components cool down to ambient temperature before further use. 

Do not repeat sterilization cycle when components are still warm.

 4 - MAINTENANCE 

 

 

The SOFFIO CUBE aerosol therapy device does not require any particular maintenance. The 

compressor does not need to be lubricated as the piston is the dry-operating type. It is advisable 

replace nebulizer after some 100 to 120 treatments on single patient or after about 20 sterilization 

cycles. Check the filter continually for cleanliness and replace it if dirty, or after a maximum of 3 

months use. Spare filters are provided with the device. To replace the filter, open the air filter slot 

(4) (if needed using a tool) and replace the filter (Fig. D).

ENGLISH • ENGLISH • ENGLISH • ENGLISH • ENGLISH • ENGLISH • ENGLISH • ENGLISH • ENGLISH • ENGLISH • ENGL

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Summary of Contents for Soffio Cube

Page 1: ...ENGLISH ITALIANO ENGLISH ISTRUZIONI D USO INSTRUCTION MANUAL Soffio Cube...

Page 2: ...Fig A 2 Fig D Soffio Cube Fig C2 Fig B Fig C1 15 7 8 9 12 13 10 11 1 3 2 5 4 6 14...

Page 3: ...orme sulla restrizione dell uso di determinate sostanze pericolose nelle apparec chiature elettriche ed elettroniche Direttiva Europea RoHS 2011 65 UE Apparecchio adatto per funzionamento continuo 1 2...

Page 4: ...solo per alimentare l ampolla L apparecchio non adatto ad un uso in presenza di miscela anestetica infiammabile con aria ossigeno o protossido di azoto Le prestazioni dell apparecchio sono garantite...

Page 5: ...al proprio medico posizionare l interruttore ON OFF 3 in posizione O per spegnere l apparecchio e staccare la spina dalla rete di alimentazione 7 Svuotare il farmaco rimanente dall ampolla nebulizzatr...

Page 6: ...SOLUZIONI L apparecchio non si accende Accertare che la spina 2 sia ben inserita nella presa di corrente Accertarsi che l interruttore ON OFF 3 sia in posizione di acceso I La nebulizzazione debole o...

Page 7: ...t Genera tion Impactor 7 SMALTIMENTO DELL APPARECCHIO E O DEI SUOI COMPONENTI Lo smaltimento dell apparecchio e o dei suoi componenti in caso di messa fuori uso deve avve nire nel rispetto delle vigen...

Page 8: ...azione Potenza di uscita nominale massima del trasmettitore W Distanza di separazione alla frequenza del trasmettitore m da 150 kHz a 80 MHz d 1 2 x P da 80 MHz a 800 MHz d 1 2 x P da 800 MHz a 2 5 GH...

Page 9: ...ezza e l affidabilit tutti i dispositivi medici prodotti da Air Liquide Medical Systems S r l sono periodicamente soggetti a revisione ed a modifiche I manuali di istruzione vengono pertanto modificat...

Page 10: ...Class II device Device with type BF applied part O Device OFF I Device ON Alternating current Important Read the warnings carefully Manufacturer Important read the instructions carefully IP21 Device p...

Page 11: ...cable is damaged Check that the casing is integral and there is no sign of dents or damage Never open the device Never bend the nebuliser over 60 The manufacturer declares that the device has a usefu...

Page 12: ...essories under warm tap water max 60 C adding if necessary a small quantity of detergent following dosage and use limitations as provided by detergent manufacturer Rinse thoroughly making sure that al...

Page 13: ...sure at the device 1 85 bar Maximum air flow at the device 10 l min Operating air flow with the nebulizer 5 l min Nebulizing rate with NaCl 0 9 solution 0 35 ml min Maximum absorbed power 150 VA Dimen...

Page 14: ...01 1 2 2015 on the electromagnetic compatibility of medical devices Compliance with electromagnetic compatibility standards does not guarantee total immunity of the product Some devices mobile phones...

Page 15: ...rer is liable for the safety reliability and performance of the device provided that it is used in accordance with the instructions and for the intended purpose only and any repairs are carried out by...

Page 16: ...ogettato e costruito da The device described herein was designed and built by COD 811310 REV 06 2020 0051 Air Liquide Medical Systems S r l Via dei Prati 62 25073 Bovezzo BS ITALY Tel 39 030 201 59 11...

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