Manual Lanaform LA120420 (page 8 of 60) (English, German, Dutch, French, Italian, Spanish)

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8 / 60 CN-100 P

EN FR NL DE ES IT SL BG

No nebulisation or

nebulisation speed slow

when the device is on.

Does the drug reservoir

contain any of the drug?

Add the appropriate volume of

the drug to the drug reservoir.

Does the drug reservoir

contain too much or not

enough of the drug?

Is the spray cap missing or

not assembled correctly?

Attach the spray cap correctly.

Has the nebulisation kit

been correctly assembled?

Assemble the nebulisation

kit correctly.

Is the cannula blocked?

Check that the cannula

is not obstructed.

Is the nebulisation kit tilted

at too steep an angle?

Make sure that the nebuli-

sation kit is not tilting at an

angle of more than 45 degrees.

Is the air tube connected

correctly?

Check that the air tube is

correctly attached to the com-

pressor and nebulisation kit.

Is the air tube folded

or damaged?

Check that the air tube

is not twisted.

Is the air tube blocked?

Check that there air tube

is clear of obstructions.

Is the air lter dirty?

Replace the air lter

with a brand new one.

The device is unusually noisy.

Has the air lter cover

been correctly attached?

Attach the air lter

cover correctly?

The device is very hot. Is the compressor covered?

Do not cover the compressor

with anything when in use.

If the solution suggested does not resolve the problem, do not try to repair the device

since no component of the unit can be repaired by the user.

Return the unit to a retail outlet or approved LANAFORM distributor.

TECHNICAL INFORMATION

• Name: LANAFORM

• Model: CN-100P LA120420

• Type: Compression-driven nebuliser

• Nominal value (compressor with nebuliser): 1.5V x 4 AA batteries or USB 5 V 1A

• Operating conditions: Operates intermittently: 20 mins. on/40 mins. o

• Temperature/Moisture content when running : +5°C to +40°C/15% at 85% HR

•

Temperat ure/Mois ture content when stored: -25° C to +35°C with relati ve humidit y below

90°C with no condensation and between 35°C and 70°C with water vapour up to 50hPa

• Atmospheric pressure: HR 700 - 1,060 hPa

• Weight: Approximately 180g (compressor only)

• Dimensions: Approximately 115 (L) x 77 (H) x 42 (P) mm

• Contents: Compressor, nebulisation kit, tube à air (PVC, 100cm), replacement air lters

(5 units), mouth piece, adult’s mask (PVC), children’s mask (PVC), USB cable, storage

bag, instructions for use.

• Operating time: 15 minutes on/40 minutes o.

•

Built-in timer: The compressor runs for 15 minutes once the on/o button has been

pressed and then stops.

• Compression output: 2-10/min

• Compression pressure: 360-550mmHg

• May be changed without prior notice.

• The device may not run if the temperature and voltage are dierent from those dened

in the technical features.

• Do not use the device in places where it might be exposed to ammable gases.

•

This device complies with the provisions of European Community Directive 93/42/EEC

(Directive on medical devices) and European standard EN13544-1:2007, Oxygen Therapy

Equipment - Part 1: Nebulisation systems and their components.

TECHNICAL INFORMATION ON THE COMPRESSOR WITH NEBULISATION KIT

Volume of the appropriate drug. 2ml minimum - 10ml maximum

Drug reservoir capacity: 10ml maximum

Size of the particles:

**MMAD Approximately 3.9 μm

MMAD = mass median aerodynamic diameter

Nebulisation rate: Approximately 0.3ml/min (depending on weight loss)

Acoustics: Approximately 58dB at a distance of 1 metre

Aerosol outlet: 0,3627 ml (1 % M/V) NaF

Aerosol output: 0,045 ml/min (1 % M/V) NaF/min

Per formance may vary with cer tain drugs such as suspensions or drugs with high viscosit y.

Consult the drug supplier’s data sheet for further details.

** Measurements taken independently according to standard EN 13544-1.

IMPORTANT INFORMATION ABOUT

ELECTROMAGNETIC COMPATIBILITY (EMC)

With the increase in the number of electronic devices such as the PC and mobile (cell)

phones, medical devices can be subject when in use to electromagnetic interference

released by other devices. Electromagnetic interference can disturb the operation of

the medical device and create a potentially dangerous situation.

Medical devices must not interfere with other devices either.

In order to regulate the requirements relating to the EMC (electromagnetic compatibility)

with the aim of preventing any dangerous situation arising caused by the product, the

EN 60601-1-2:2007 standard has been implemented. This standard denes the degrees

of immunity to electromagnetic interference as well as the maximum levels of electro-

magnetic emissions for medial devices.

This medical device complies with this EN 60601-1-2:2007 standard both in terms of

immunity and emissions.

It is nevertheless important to take special precautions:

Do not use mobile (cell) phones and other devices that generate powerful electrical or

electromagnetic elds close to the device. This might disturb the operation of the medical

device and create a potentially dangerous situation. Keeping a minimum distance of 7m

away is recommended. Check that the device is running properly if it is closer than this.

ADVICE REGARDING

THE DISPOSAL OF WASTE

All the packaging is composed of materials that pose no hazard for the environment and

which can be disposed of at your local sorting centre to be used as secondar y raw materials.

The cardboard may be disposed of in a paper recycling bin. The packaging lm must be

taken to your local sorting and recycling centre.

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Lanaform LA120420 Manual

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