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•   Do not put the device near heat sources, direct sunlight, or in  

hot environments.

•   Do not obstruct or insert any objects in the filter or in its housing in  

the device.

•  Do not obstruct the air vents placed on both sides of the unit.
•   During use, always place the unit on a firm surface clear of obstacles.
•   Check that there is no material obstructing the air vents before each use.
•  Do not place any objects inside the air vents.
•   Repairs, including the replacement of the power cord, must be performed 

by authorized personnel only following the information provided by the 
Manufacturer. Any unauthorized repairs will void the warranty and may 
pose a safety hazard for the user.

•  The average duration provided for compressor is: 2000 hours.

    

 

Do not modify this equipment without authorization of the 

manufacturer.

•   The Manufacturer, the Retailer and the Importer are responsible for the sa-

fety, reliability and performance of the device only if: a) the device is used 
in accordance with the operating instructions b) the electrical system of 
the premises where the device is used is in compliance with current laws.

•   Interactions:

 The materials used that come into contact with medications 

have been tested with a wide range of medications. However, due to the 
variety and continuous evolution of medications, the possibility of a che-
mical interaction cannot be excluded. We recommend that once the medi-
cation has been opened you should use it as soon as possible and avoid 
prolonged contact of the medication with the nebulizer.

•   The manufacturer should be contacted for reporting problems and/or 

unexpected events related to device operation and if necessary for clarifi-
cations on use, maintenance or cleaning.

Before using the device for the first time, and periodically during the pro-
duct’s life, check the integrity of its structure and of the power cable,  
making sure that there is no damage; if it is damaged, do not insert the  
plug and take the product immediately to MPV MEDICAL or to an authorized 
local dealer.

•  This Medical Device is intended also for patient‘s direct use. 
•  The average lifespan of accessories is 1 year; however, we recommend 

you replace the nebulizer every 6 months in intensive use (or earlier, if the 
nebulizer is blocked) to always ensure maximum therapeutic effect.

•  If the device is not performing according to the specification, please  

contact an authorized service centre or distributor.

•  Children and disabled persons should always use the unit under strict 

supervision of an adult who has read this manual.

•  Several parts of the device are small enough to be swallowed by children; 

therefore keep the device out of reach of children.

•  Do not use the tubes and the cords of the device for purposes other than 

those specified as they may cause strangulation hazard; utmost attention 
must be paid to children and persons with special needs; usually, such 
persons are not capable of assessing the hazard correctly.

•  The unit should not be used in the presence of anaesthetic mixture inflam-

mable with air, oxygen or nitrous oxide.

•  Keep the cord away from heated surfaces.
•   Keep the power supply cord away from animals (for example rodents) as 

they may damage the insulation of the power supply cord.

•   Do not handle the unit with wet hands. Do not use the device in humid 

environments (e.g. while taking a bath or shower). Do not immerse the de-
vice in water; should this accidentally occur, unplug the device immedia-
tely. Do not remove or touch the device immersed in water before pulling 
out the plug. Take the device immediately to an authorized service centre 
or to your local dealer.

•   Only use the device in dust-free environments; otherwise, therapy may  

be compromised.

•  Do not wash the device under running water or submerge in water.  

Keep away from splashing water or other liquids.

•  Do not expose the device to particularly extreme temperatures.

Important safeguards

Summary of Contents for MicroDrop Pro2

Page 1: ...MicroDrop Pro2 plus Gebrauchsanweisung Instruction Manual www mpvmedical com DE EN...

Page 2: ...en Wir begl ckw nschen Sie zu Ihrem Kauf und danken Ihnen f r Ihr Vertrauen Wir haben uns zum Ziel gesetzt den Vorstellungen unserer Kunden gerecht zu werden und moderne Produkte f r die Behandlung vo...

Page 3: ...Kompressor A2 Ein Ausschalter A3 Schlauchanschluss A4 Luftfilter B5 Tragegriff C6 Verneblerhalter C7 Kabelraum C8 Netzkabel D1 Soft Maske f r Kinder D2 Soft Maske f r Erwachsene D3 Mundst ck mit Vent...

Page 4: ...ndt werden Kosten f r den Transport des Ger ts gehen zu Lasten des Kunden Reparaturen die nicht unter die Garantiebedingungen fallen gehen zu Lasten des Kunden Die Garantie deckt keine Sch den ab die...

Page 5: ...gung Vor der ersten Verwendung und in regelm igen Abst nden w hrend der Lebensdauer des Produkts muss die Unversehrtheit der Ger testruktur und des Versorgungskabels gepr ft werden um sicherzustellen...

Page 6: ...zeigersinn 4 Schlie en Sie die Zubeh rteile gem Anschlussschema an Setzen Sie sich bequem hin und halten Sie den Vernebler in der Hand Bringen Sie das Mundst ck an den Mund oder benutzen Sie die Maske...

Page 7: ...tives Begrenzungsventil wird die Me dikamentenabgabe an die Umge bung reduziert Das spart Medika ment und garantiert eine effektive Medikamentenablage rung in den unteren Atemwegen W hrend der Einatem...

Page 8: ...Bitte folgen Sie streng den Anweisungen des Desinfektionsmittelherstellers vor allem in Bezug auf Sicherheitshinweise Konzentration Dosierung und Einwirkzeit Bereits gebrauchsfertige L sungen die Sie...

Page 9: ...0 Minuten und einerTemperatur von 134 C gem der Bedienungsanleitung des Ger ts durch Lagerung lagern Sie die sterilisiertenTeile gem der Gebrauchsanweisung des Sterilbarrieresystems Das Sterilisations...

Page 10: ...de Ger t als Abfall eingestuft wird und somit der M lltrennung unterliegt Der Verbraucher muss ge nannten Abfall den von den Kommunalverwaltungen eingerichteten Sammel stellen zuf hren bzw zuf hren la...

Page 11: ...erhalten Sie auf Anfrage Spannung 230V 50Hz 210VA Entspricht der Richtlinie 93 42 EWG und nachfolgenden Modifikationen Max Druck 3 5 0 5 bar Luftleistung Kompressor ca 14 l min Ger uschpegel 1 m Absta...

Page 12: ...fessionelles Inhalationsger t mit besonders kleinen Aerosolteilchen Lieferumfang Kompressor RF7 plus Vernebler Soft Kinder und Soft Erwachsenenmaske Mundst ck Druckluftschlauch manuelles Trigger T St...

Page 13: ...DE 1 MicroDrop Pro2 plus Instruction Manual www mpvmedical com EN...

Page 14: ...ed by a doctor who has performed patient s eva luation Visit our Internet site www mpvmedical com to view the whole range of MPV MEDICAL products Product description Page Product description 3 Complet...

Page 15: ...f switch A3 Air outlet port A4 Air filter B5 Carrying handle C6 Nebulizer holder C7 Cable compartment C8 Power cord Pic C 6 7 8 Pic B Pic A 1 2 4 3 D1 Soft child mask D2 Soft adult mask D3 Mouthpiece...

Page 16: ...after the defect is noticed Transport costs for the device are at user s charge Any repair out of warranty conditions are at user s charge The warranty does not cover failures resulting from misuse a...

Page 17: ...f the power cable making sure that there is no damage if it is damaged do not insert the plug and take the product immediately to MPV MEDICAL or to an authorized local dealer This Medical Device is in...

Page 18: ...ebulizer by turning the upper part Pic E1 clockwise 4 Connect the accessories as shown in the Assembly diagram Sit com fortably holding the nebulizer in your hands place the mouthpiece over your mouth...

Page 19: ...ry phase the tab acting as a Dispersion Li miting Device bends inwards towards the mask During the expiratory phase the tab acting as a Dispersion Limit ing Device bends out wards from the mask Using...

Page 20: ...tion dosage and exposure time Ready to use solutions that you do not need to mix yourself can be bought on the internet or in pharmacies b Immerse each component completely in the solution Make sure t...

Page 21: ...rage Store the sterilized parts according to the instructions for use of the sterile barrier system The sterilization procedure has been validated in conformity with ISO 17665 1 Use original manufactu...

Page 22: ...st there fore undergo sorted waste collection The user must therefore take or have taken the above waste to a pre sorted waste collection centre set up by the local authorities or else give it back to...

Page 23: ...ications Max Pressure 3 5 0 5 bar Compressor air output 14 LPM approx Noise level at 1 m 57 dB A approx Operation Continuous use Dimensions W x D x H 180 mm x 200 mm x 110 mm Weight 1 8 kg Applied par...

Page 24: ...3900 MicroDrop Pro2 plus Filter Compressor 1 piece for new compressor series MicroDrop Pro2 plus Professional inhalation with extra small particles Including Compressor RF7 plus nebulizer Soft child a...

Page 25: ...r EU Richtlinie 93 42 EEC und nachfolgenden nderungen THIS DEVICE FULFILSTHE PROVISIONS OFTHE EC DIRECTIVE 93 42 EEC AND SUBSEQUENT MODIFICATIONS Hersteller MANUFACTURER 93 42 EEC Designed und entwick...

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