Flaem Respir Air handleiding

Handleiding

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6

Respirair

Mod.: P0611EM F1000

MaxPressure: 2.6±0.4bar

Compressorairoutput: 10l/minapprox

Noiselevel(at1m): 54dB(A)approx

Operation: Continuous use

Dimensions(L)x(P)x(H): 16x16x10cm

Weight: 1.45Kg

Operating conditions:

Temperature: min10°C;max40°C

Airhumidity: min10%;max95%

Atmosphericpressure: min69KPa;max106KPa

Storage conditions:

Temperature: min-25°C;max70°C

Airhumidity: min10%;max95%

Atmosphericpressure: min69KPa;max106KPa

APPLIED PARTS

TypeBFappliedpartsinclude: (C2,C3,C4)

RF7 DUAL SPEED PLUS Nebulizer

Medication minimum capacity: 2 ml

Medication maximum capacity: 8 ml

Operatingpressure(withneb.): 0.90bar

TECHNICAL DATA

Voltage: 230V~50Hz140VA115V~60Hz220V~60Hz100V~50/60Hz

Safety certications:

DEVICE DISPOSAL

In conformity with Directive 2002/96/EC, the symbol shown on the device to be disposed of

indicatesthatitisconsideredaswasteand isthereforesubjectto“sortedwastecollection”.The

user musttherefore deliver (orhave delivered) theabove wasteto an appropriate wastecollection

centreprovidedbythelocalauthorities,ordeliverittothedealerwhenpurchasinganewappliance

ofthe sametype.Pre-sortedwaste collectionandthe subsequenttreatment,recoveryand disposal

operations favor the production of appliances made of recycled materials and Iimit the negative eects

to the environment and public health due to incorrect waste management. The unlawful disposal of the

product by the user could result in administrative nes as provided by the laws transposing Directive

2002/96/ECoftheEuropeanmemberstateorofthecountryinwhichtheproductisdisposedof.

ELECTROMAGNETIC COMPATIBILITY

This device has been designed to satisfy requirements currently required for electromagnetic

compatibility(EN60601-1-2:2007).Electricalmedicaldevicesrequirespecialcare.Duringinstallationand

usewithrespecttoEMCrequirements,itthereforerequiredthattheybeinstalledand/orusedaccording

tothemanufacturer’sspecication.Potentialriskofelectromagneticinterferencewithotherdevices,in

particular with other devices for analysis and treatment. Radio and mobile telecommunications devices

orportableRF(mobilephonesorwirelessconnections)mayinterferewiththeoperationofelectrical

medical devices.For further informationvisit www.aemnuova.it.Flaem reserves the rightto make

technical and functional changes to the product without notice.

Speed selector C1.4

in pos Max

Speed selector C1.4

in pos Min with valve

(1)

Delivery: 0.53ml/minapprox. 0.23ml/minapprox.

(2)

MMAD: 2.53 μm 2.72 μm

(2)

Breathable fractions < 5 m (FPF): 79.6% 77.8%

(1)

datadetectedaccordingtoFlaemI29-P07.5internalprocedure

(2)

In vitro characterization certied by TÜV Rheinland Product Safety GmbH - Germany in compliance with the new European Standard for aerosol

therapyunits,StandardEN13544-1,ANNEXCC.Furtherdetailsareavailableonrequest.

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Bekijk gratis de handleiding van Flaem Respir Air, stel vragen en lees de antwoorden op veelvoorkomende problemen, of gebruik onze assistent om sneller informatie in de handleiding te vinden of uitleg te krijgen over specifieke functies.

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