QUICK GUIDE
OVERVIEW
DOCLASER® / DOCLASER® SPORT is a Class-IV
laser device, certified and classified as a medical instru-
ment in Class 2b (93/42/EEC, 47/2007EEC). It differs
from normal therapeutic laser instruments as it is desi-
gned to provide for ‘self-administered treatment’.
Please note that it is very important to read and review
the content of the enclosed manual (CD) before using this
device.
The device bears the marking 0068.
PROCEDURE FOR USE
• Switch on the device by pressing the ‘OK’ key for
about 5 seconds
• At the first start-up select language
• Wait until the software asks you to insert the password
• Insert the password: UP, DOWN, LEFT, RIGHT
CONTRAINDICATIONS
Suspected or fully-developed neoplasia, pregnancy,
haemorrhagic areas, epilepsy, infected areas (contami-
nated, open wounds), herpes zoster / herpes simplex,
general states of infection, children under the age of 16,
direct exposure to the eyes.
N.B.: no particular precaution is required during tre-
atment in the case of persons with prostheses or a pace-
maker or in the case of diabetes.
It should be noted that for all persons who have re-
ceived radio or chemotherapy any physical therapy is
contraindicated for a period of 5 years following the last
session of treatment.
ORDINARY MAINTENANCE
DOCLASER® / DOCLASER® SPORT must be stored
in its case, protected against sources of intense heat. It
must not be kept in an environment where temperatu-
res will remain low (< 10°C) for long periods of time.
Failure to respect this condition will immediately result
in the laser not being usable.
The circular head, which comes into contact with the
skin during treatment, must also be cleaned.
EXCLUSIVE PROTOCOL
The treatment protocol to be followed is selected by
the DOCLASER® / DOCLASER® SPORT software on
the basis of a daily, multi-treatment approach, in which
the protocol to be used is selected on the basis of the
following input:
• Specific painful area of the body
• Self-evaluation of pain
• Treatment day (number)
TECHNICAL DATA: LASER MODEL AG6 DOCLASER® /
DOCLASER® SPORT
Rated power (Pnom) - IEC EN 60825-1 up to 2 W
Spot size with applicator in contact 10 mm
Wavelength 630 - 1064 nm
Beam divergence 8° x 36°
Power density with applicator up to 1.4 W/cm
2
max
Operation discontinuous
CHANGE LANGUAGE
It is possible come back to language selection inserting,
during the DOCLASER® / DOCLASER® SPORT pas-
sword request, the following sequence:
LEFT, RIGHT, UP, DOWN.
RESTORE FACTORY CONFIGURATION
To reinstate DOCLASER® / DOCLASER® SPORT to
factory configuration inserting, during the password
request, the following keys sequence:
DOWN, RIGHT, UP, LEFT.
INSTRUCTIONS FOR DISPOSAL
When the instrument is no longer needed and has rea-
ched the end of its working life, it should not be dispo-
sed of just like any other waste product but delivered
to a differentiated refuse collection site for electronic
equipment or simply returned to the retailer from
whom it was purchased when a new laser source has
to be purchased.
WARRANTY
The DOCLASER® / DOCLASER® SPORT model
medical device is guaranteed for a period of two years
against breakage and failure of its components and any
consequent repair work that may be required.
PRODUCER
DOCLASER® / DOCLASER® SPORT are produced
by TOUCH LIFE REHAB S.r.l.unip.| Via A. Amighetti,
2/A 24125, Bergamo, Italy
