LaBina PL-2000 User manual

Operating Manual

Operation
The power supply should be connected with the corresponding socket.
The red LED illuminates when the device is connected with the power supply
system.
The handpieces should be connected with the corresponding socket.
Switch on the device with the on-off button; the power LED is off. Press it again to
switch the device off.
The welcome screen will appear on the display; it can be skipped with every
button.
The handpiece can be chosen. It is shown on the display.
The speed is shown on the display.
By pressing plus or minus, the speed can be altered.
The GO button switches the handpiece on.
The green LED illuminates to show that a handpiece is in operation.
The laserhandpiece should be connected with the corresponding socket.
The laser button activates the stand-by mode of the laser handpiece.
The start button switches the laserhandpiece on.
The yellow LED illuminates to show that the laserhandpiece is in operation.
The foot pedal should be connected with the corresponding socket.
The handpiece will be switched on and off by pressing the foot pedal.
Control unit
Start-up
The device is designed to be used on a table, i.e. it has to be placed on a firm and level
surface.
The clearly marked connecting sockets for the mains power supply and the handpiece are
at the rear of the appliance. The appliance is ready for operation when it is connected to
the power supply unit and thus the mains. This is indicated by a red light.
During breaks, the handpiece must only be placed onto the holder which should
be covered with a protective film.
Only use the device with the power supply as specified on the device’s rating plate. The
mains voltage must be the same as the rated voltage of the device as printed on the power
supply.
The device is only designed for internal use. It can be operated without impairment at
room temperatures ranging from 10 °C to 35 °C. Please make sure prior to using the de-
vice that it has adapted to room temperature; otherwise, condensation could damage the
electronics (a temperature differential of 10 °C requires a minimum three hour).
Safe operation cannot be guaranteed:
• If the device or its accessories show signs of damage,
• if the device does not work properly,
• after longer-term storage outside of the prescribed temperature range,
• in cases of transport damage if the device has been improperly transported.
In these cases the device should always be returned to the authorized specialist dealer/
supplier for inspection.
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Operating Manual
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Technische Parameter
Rated voltage: 15 V – (DC)
Power input: 7 VA max
Power supply unit: as listed on the type indication plate
Safety class: 2
Operating conditions:
Ambient temperature: +10 °C to +35 °C
Relative humidity: 30% to 75%
V 3.0, 07/2012


Areas of application / purpose of use
The most common cosmetic applications for micro-pigmentation are:
• eyebrows
• eyeliner
• full lip colour or lip liner (improving the lip contours)
• body tattoos
Operating Manual
Permanent Make Up handpiece
Effectiveness
During the pigmentation process a fine needle penetrates the skin inserting a colour
pigment into the upper layer of the skin, creating a line that replaces the need for a daily
application of either eyebrow pencil, eyeliner or lip liner.
A micropigmentation lasts several years depending on type of skin and colour but a mini-
mum durability or a total fading cannot be guaranteed. It is possible, that the color cannot
be removed, residues of the color could stay in the skin or scarring could occur.
During the initial 4 to 6 weeks, the intensity of the applied colour that has been applied
fades to its „permanent level“. This is normal, because the epidermis (upper level of the
skin) renews itself and the pigments within this layer of the skin grows out. The
remaining visible colour is beneath the epidermis. The thickness of the epidermis varies
from person to person and also depends on area the body treated.

Contra-indications
Pigmentation must not be applied to anyone with the following conditions:
• Hemophilia • Infectious disease
• Hepatitis A, B, C, D, E, F • Skin blemish in the area of pigmentation
• HIV-positive (e.g. eczema, warts, melanoma)
• Keloid formation • Immune system desease
• Cardiac and circulatory troubles • Allergies
• Conjunctivitis (contraindicated in case of lip pigmentation)
• Epilepsy • Pregnancy or lactation
• Diabetes II
• Under the influence of alcohol or drugs
• Taking of coagulation-inhibiting or blood-dilutiving pharmaceuticals
or pharmaceuticals against menstrual cramps
• Taking certain prescription drugs (consult the prescribing physician)
If there is even the slightest concern regarding the safety of the customer, the treatment
must not be started or respectively must be stopped immediately and medical consent
sought.
Treatment must be stopped immediately in the following cases:
• the customer feels excessive pain
• excessive fluid is discharged from the wounds
• the customer feels faint or dizzy
Special caution is required under following circumstances:
• Patients suffering under herpes simplex and undergoing micropigmentation of the lips
are likely to develop herpes labialis (cold sores). Consulting a physician and prophylaxis is
recommended.
• Patients undergoing chemotherapy should not receive micropigmentation during the time
of 4 weeks before chemotherapy until 4 weeks after chemotherapy. During this time color
pigments will be implemented in the skin poorly.

Pen
Note: The handpiece and especially the drive inside is a mechanical precision instrument
and must not be soiled. Therefore colour must not get into the drive. Easily flowing co-
lours support the running back effect.
There is a risk of contaminated colour running back down into the machanism. Therefore
investigate the handpiece carefully prior to use. Do not use it if contamination is suspec-
ted. It is important not to break the cable of the handpiece.
Damage due to colour penetrated into the driveshaft shall not be recognised as a reason
for complaint and repair must be paid by the client.
Safety cartridge
Essential: for the use of the safety cartridge, please take heed of Chapter „Important
hygiene and safety instructions“.
All cartridges are labelked with the lot number, date of manufacture, and use-by date.
The lot number helps with the clear identification of the batch and has been issued by
manufacturer in case of any problems. The lot number has to be noted in the customer‘s
file.
Provided the packaging is closed and not damaged, the cartridge manufacturer
guarantees their sterility for 5 years under conditions as set out in chapter “Transport
and storage conditions”. The cartridges have to be stored in their original packs of ten.
The cartridge is screwed into the handpiece. Test the cartridge for secure fit to the
handpiece immediately after fitting it.
Fill the cartridge with 2 or 3 drops of colour.
Alternatively, the cartridge tip can be dipped into the colour for 2 to 3 seconds. When the
device is switched on, the colour is sucked up into the cartridge. Avoid any contact with
the tip of the needle and the colour container during this procedure.
Adjusting of depth of penetration
Only adjust the depth of penetration while the device is running. Turn the safety cartridge
to achieve the optimum needle projection for each respective purpose.
The correct needle projection depends on the application, on the skin type, the desired
effect, and other factors. This expertise needs to be acquired in a training course.
Hold the pen tight
NADELVERSTELLUNG
Injection depth adjustable
by turning the rear pen part
The needle is individually
adjustable by further screwing
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1Attach the cartridge
AUFSETZEN DES MODULS
Turn the cartridge
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Removal of the safety cartridge
Unscrew the safety cartridge to remove it from the handpiece, taking care that any remaining colour
does not run back into the handpiece. Always make sure after removing the cartridge that the need-
le is completely retracted into the cartridge in order to avoid injuries.
Disinfection/Sterilisation
A new cartridge must be used for each client and every subsequent treatment.
The cartridges are designed for single use and must only be used once.
The cartridges are sterilised and packed in a sterile way by the manufacturer of the device.
Use only sterile needles that are taken out of the sterile packaging immediately before use.
The holders and the protecting caps for the hand piece and the handle of the hand piece
must also be cleaned and disinfected immediately prior to use, before the treatment
of each client. Each piece must be treated with the appropriate disinfectant (the holder
normally by wiping it with a soft damp cloth and disinfectant, protecting caps and
handles by putting them into the solution). Please ask your distributor about sterilised
disposable protecting caps.
It is important to use the exclusively DGHM admitted disinfectants which go with the materials and
surfaces of the device pieces:
The manufacturing firm recommends the disinfectant Lysetol® Med of the company Schül
ke & Mayr. The handle of the hand piece should be cleaned periodically in an ultrasound
bath (Lysetol® Med is suitable for ultrasound). The handpiece never be immersed in desinfectant
as the internatl parts can corrode. Such damage does not come within the warranty. The national
hygiene guidelines have to be followed.
Technische Parameter
Rated voltage: 12 V – (DC)
Power input: 1,5 W max
Working frequency: selectable from 50 to 150
penetrations per second
Drive: Precision DC motor
Operating mode: Continuous operation
Operating conditions:
Ambient temperature: +10 °C to +35 °C
Relative humidity: 30% to 75%
length, diameter 135 mm, 21 mm
Weight of handpiece: c. 80 g
V 3.1, 05/2019
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