FLAEM Lella Manual De Instrucciones página 11

- Fill a container big enough to hold all of the parts to disinfect with a solution 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 bubbles on the parts.
Leave the parts immersed for the amount of time indicated on the packaging of the disinfectant associated with
the concentration chosen for the solution.
- Remove the disinfected parts and rinse abundantly with warm potable water.
- Dispose of the solution following the instructions provided by the disinfectant manufacturer.
method B: Disinfect the accessories C1.1-C1.2-C1.3-C1.4-C2-C5.1A-C5.1B-C5.1C-C5.2-C5.3-C5.4-C5.5.1-
C5.5.2-C6 by boiling them in water for 10 minutes; use demineralised or distilled water to prevent calcium deposits.
method C: Disinfect the accessories 1C1.1-C1.2-C1.3-C1.4-C2-C5.1A-C5.1B-C5.1C-C5.2-C5.3-C5.4-C5.5.1-
C5.5.2-C6 with a hot steam steriliser for baby-bottle (not the microwave type). Perform the process faithfully fol-
lowing the instructions of the steriliser. To ensure that the disinfection is effective, choose a steriliser with an oper-
ating cycle of at least 6 minutes.
After having disinfected the accessories, shake them vigorously and place them on a paper towel. Alternatively,
dry them with a jet of hot air (for example, from a hair dryer).
AIR FILTERING
The unit is equipped with an air filter (A3) which should be replaced when dirty or when its
colour changes. Do not wash or re-use the used filter. The filter must be regularly replaced
to help ensure efficient compressor performance. The filter should be regularly checked.
For spare filters contact your dealer or an authorised service centre.
To replace the filter:
Lift the lid and remove the filter using a screwdriver (see fig.). The filter is designed
to remain fixed in its housing.
Use only Flaem original accessories.
SYMBOLS
EC Marking medical ref. Dir 93/42 EEC and
subsequent updates
Class II device
Attention: check the instructions for use
"OFF" for part of Equipment
"ON" for part of equipment
In compliance with: European Standard EN
10993-1 ''Biological Evaluation of medical
devices'' and European Directive 93/42/EEC
"Medical Devices. "
Phthalate-free. In compliance with: Reg. (EC)
no. 1907/2006
All manuals and user guides at all-guides.com
TÜV approval ref. EN 60601-1 3rd Ed. - EN 60601-1-11
Device serial number
Manufacturer
Type BF applied part
Alternating current
Risk: electrocution.
Consequence: Death.
Using the device while taking a bath or shower
is prohibited
Keep dry
11
(A3)