Magic Care MIZAR Instructions For Use Manual Download Page 21

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ELECTROMAGNETIC COMPATIBILITY                                                                        

This device was designed to satisfy the currently required requisites for electromagnetic 

compatibility (EN 60601-1-2:2015). Electro-medical devices require particular care 

during installation and use relative to EMC requirements. Users are therefore requested 

to install and/or use these devices following the manufacturer’s specifications. There 

is a risk of potential electromagnetic interference with other devices. RF mobile or 

portable radio and telecommunications devices (mobile telephones or wireless 

connections) can interfere with the functioning of electro-medical devices. For 

further information visit our website www.flaemnuova.it. The device may be subject 

to electromagnetic interference if other devices are used for specific diagnosis or 

treatments. Flaem reserves the right to make technical and functional modifications 

to the product with no prior warning.

DEVICE DISPOSAL                                                                                                                          

In compliance with the Directive 2012/19/EC, the symbol printed on the 

device shows that the device to be disposed of is considered waste and must 

therefore be an item of ‘’differentiated collection’’. Consequently, the user must 

take it (or have it taken) to the designated collection sites provided by the local 

authorities, or turn it in to the dealer when purchasing an equivalent new device. 

Differentiated waste collection and the subsequent treatment, recycling and disposal 

procedures promote the production of devices made with recycled materials and limit 

the negative effects on the environment and on health caused by potential improper 

waste management. The unlawful disposal of the product by the user could result in 

administrative fines as provided by the laws transposing Directive 2012/19/EC of the 

European member state or of the country in which the product is disposed of.

Summary of Contents for MIZAR

Page 1: ...INSTRUCTION FOR USE MANUAL Schema di collegamento Assembly diagram MIZAR C C5 C4 C2 C3 C1 C1 1 C1 2 C1 2 1 C1 2 2 C1 2 3 C1 C1 2 B A C6 C6 C6 1 C6 2 C6 3 C6 4 C6 5 Accessory Bag D A1 A3 A2 A4 A5 E E1...

Page 2: ......

Page 3: ...el trattamento delle malattie delle vie respiratorie Leggete attentamente queste istruzioni e conservatele per consultazioni future Utilizzate l accessorio solo come descritto nel presente manuale Que...

Page 4: ...ienti privi di polvere altrimenti la terapia potrebbe essere compromessa Non lavate l apparecchio sotto acqua corrente o per immersione e tenetelo al riparo da schizzi d acqua o da altri liquidi Non e...

Page 5: ...C1 2 1 C1 2 2...

Page 6: ...n questo caso otterrete un ac quisizione ottimale del farmaco riducendo al minimo la dispersio ne dello stesso nell ambiente circostante ISTRUZIONI D USO CON DOCCIA NASALE RHINO CLEAR ERGO Prima di og...

Page 7: ...Inserite l adattatore nasale C6 5 5 Collegate la doccia nasale all apparecchio mediante il tubo B e il raccordo C6 1 6 Mettete in funzione l apparecchio azionando l interruttore A1 7 Avvicinate al nas...

Page 8: ...isinfettante stesso Immergere completamente ogni singolo componente nella soluzione avendo cura di evitare la formazione di bolle d aria a contatto con i componenti Lasciare i componenti immersi per i...

Page 9: ...sso con un dito Protetto contro la caduta verticale di gocce d acqua Temperatura ambiente minima e massima Umidit aria minima e massima Pressione atmosferica minima e massima Alimentatore per uso dome...

Page 10: ...te di tipo BF sono accessori paziente C2 C3 C4 C5 C6 5 Nebulizzatore RF8 Dual Speed Capacit minima farmaco 2 ml Capacit massima farmaco 8 ml Pressione d esercizio con neb 0 8 bar CARATTERISTICHE TECNI...

Page 11: ...tore ostruito Smontare il nebulizzatore togliere l ugello e provvede re alle operazioni di pulizia La mancata pulizia del nebulizzatore dai depositi di medicinale ne compromette l efficienza ed il fun...

Page 12: ...riserva il diritto di apportare modifiche tecniche e funzionali al prodotto senza alcun preavviso SMALTIMENTO DELL APPARECCHIO In conformit alla Direttiva 2012 19 CE il simbolo riportato sull apparec...

Page 13: ...ory tract ailments Carefully read these instructions and keep them in a safe place for future reference Read these instructions carefully and retain them for future reference Only use the accessory as...

Page 14: ...being sprayed by water or other liquids Do not expose the device to particularly extreme temperatures Do not place the device near sources of heat in direct sunlight or in excessively hot rooms Alway...

Page 15: ...C1 2 1 C1 2 2...

Page 16: ...smitting infections During application it is advisable to suitably protect yourself from any dripping 1 Insert the L jack E1 of the power supply cord into socket A5 and then connect it to a mains outl...

Page 17: ...vinegar then rinse thoroughly under potable hot water approximately 40 C If you want to also perform the cleaning for DISINFECTION jump to the DISINFECTION paragraph After having sanitised the accesso...

Page 18: ...of potable water and disinfectant according to the proportions indicated on the packaging of the disinfectant Completely immerse each part in the solution taking care to avoid the formation of air bu...

Page 19: ...bath or shower is prohibited In compliance with European Standard EN 10993 1 Biologi cal Evaluation of medical devices and European Directive 93 42 EEC Medical Devices Phthalate free In compliance wit...

Page 20: ...ts are patient accessories C2 C3 C4 C5 C6 5 RF8 Dual Speed nebuliser Medication minimum capacity 2 ml Medication maximum capacity 8 ml Operating pressure with neb 0 8 bar TECHNICAL SPECIFICATIONS C1 2...

Page 21: ...the right to make technical and functional modifications to the product with no prior warning DEVICE DISPOSAL In compliance with the Directive 2012 19 EC the symbol printed on the device shows that t...

Page 22: ...ffects its efficiency and operation Strictly comply with the instructions contained in the CLEANING SANITISATION AND DISINFECTION chapter The air pipe is not correctly connected to the device Ensure t...

Page 23: ...23...

Page 24: ...NUOVA S p A Via Colli Storici 221 25015 S MARTINO DELLA BATTAGLIA Brescia ITALY Tel 39 030 9910168 r a Fax 39 030 9910287 www flaemnuova it 2017 FLAEM NUOVA All right reserved cod 17495A0 Rev 03 2017...

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