Gima PRIMALED User manual

Operative Manual
MO079-IT
15/06/12
Rev.0
Pag. 1 di 16
Operative manual for diagnosis lamp
PRIMALED
PRIMALED-FLEX
Via Marconi, 1 –20060 GESSATE (MI) ITALIA
Tel. [phone] Fax [phone]
http://www.gimaitaly.com e-mail: gim[email protected]
TABLE OF CONTENTS
Pag.
Introduction
1. General information
2
2
1.1
Qualification of operators
3
1.2
Packaging, transport, storage and characteristics of the installation site
3
1.3
Graphic symbols used on the Product and packaging
3
1.4
CE Declaration of Conformity of the Manufacturer
4
1.5
Warranty Certificate
5
2. Product Installation
6
2.1
Installation mobile version
6
2.2
Installation wall version (S/12MED fixing)
6
2.3
Installation wall version (rail bar fixing)
6
2.4
Installation table version (S11 fixing)
6
2.5
First starting
6
2.6
Installation verification and Product testing operations before use
6
3. Importance if personal safety
7
3.1
Intended use
7
3.2
Environmental conditions
7
3.3
Other secondary conditions (secondary effects)
7
4. Description of the operations
7
5. Cleaning and disinfection
8
5.1
Cleaning the Product
8
5.2
Disinfecting
8
5.3
Sterilizing the handpieces
8
6. Adjustments
9
6.1
Yearly inspections by the operator
9
6.2
Repairs
9
6.3
Adjustments
9
6.4
Troubleshooting
9
6.5
Routine maintenance
9
6.6
Spare parts list
9
7. Technical data
10
8. Electrical diagram
9. EMC Declaration
11
12
10. Friction regulation
15

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Introduction
Dear user You are kindly invited to read this manual carefully before proceeding to use the Product in order to
safeguard yourself and other people from any injuries.
This appliance is a Class 1 medical device pursuant to European Directives on medical devices (MDD) 93/42/EEC,
Annex IX, and 2007/47/EC.
The manufacturer declares that this product is in compliance with Annex I (essential requirements of Directive
93/42/EEC and certifies such conformity by affixing the CE mark.
The Product is classified in risk group 1 according to IEC 62471 standard (Photobiological Safety of Lamps).
This operator’s manual refers to the product PRIMALED/ PRIMALED-FLEX.
The customer service is at your disposal in case of Product details, information concerning its use, identification of
spare parts being required and for any other queries you might have concerning the appliance, for ordering spares
and for matters relating to assistance and warranty.
GIMA TECHNICAL ASSISTANCE OFFICE FOR CLIENTS
Via Marconi, 1 –20060 GESSATE (MI) ITALY
Tel. [phone] Fax [phone]
http://www.gimaitaly.com e-mail: [e-mail]
The contents of this Manual may be amended by GIMA, without prior notice or any further obligations, in order to
make changes and improvements. The reproduction, including partial, or translation of any part of this manual is
forbidden without the written permission of GIMA.
GIMA reserves the right to change, cancel or otherwise amend the data contained in this document at any time and
for any reason without prior notice inasmuch as GIMA is constantly seeking new solutions which lead to product
evolution. GIMA therefore reserves the right to make changes to the supplied Product in terms of shape, fittings,
technology and performances.
With regard to translations into languages other than Italian, reference shall always be made to the Italian edition of
this operator’s manual.
1. General information
The ME (Medical-Electrical) EQUIPMENT to which this manual refers is a LAMP for diagnosis or observation.
For easier description such ME EQUIPMENT will be indicated in this manual with the name of “Product”.
This manual is an integral part of the Product as required by European directive 93/42/EEC and 2007/47/EC.
Always keep this installation manual close to the Product.
The Product is not suitable for use in explosion-risk areas
- The Product is not suitable for use in the presence of inflammable mixtures of anaesthetics with air, oxygen or
NO2(laughing gas)
GIMA disclaims all liability for any injuries to persons or damage to things caused by the installation,
maintenance or use of the Product by unqualified operators. By qualified operator is meant whosoever has attended
a course relating to the installation, maintenance and use of the product organised by GIMA or, alternatively,
whosoever has carefully read this installation manual.
The only party responsible for Product installation is the buyer’s customer itself; no cost or responsibility relating to
installation and/or commissioning of the Product shall therefore be traced back and/or in any case attributed to
GIMA.
The masonry works involving the preparation of the ceiling or wall, for Products to be installed on the ceiling or
wall respectively, and the electric works for preparing the power supply system for the Product shall be of a sturdy
and safe nature and completed in a workmanlike manner by suitably trained personnel.
By way of example only, without limitation, the following professional figures are deemed adequately trained:
Building Engineer, Draughtsman, Building firm duly registered in the professional Register (for masonry works)
Electro-technician qualified to exercise the profession of electrician (for the electrical works)
The Product is a ME EQUIPMENT and consequently falls within the field of application of the EN:62353 standard.
Consequently, any operation performed on the Product must be carried out in compliance with the EN:62353
standard, where applicable.

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1.1 Qualification of operators
This paragraph describes the requirements and qualifications which the operators involved in the various stages of
Product life and use must possess.
Installation
Qualified Installer and/or Technician
Use
Professional medical personnel
Routine maintenance (about every year)
Qualified technician in possession of professional technical requirements
Special maintenance (in case of necessity)
Qualified technician in possession of professional technical requirements
Assistance
GIMA or authorized dealer
Cleaning
Properly trained medical and paramedical personnel
Demolition
In compliance with the national directives applicable to waste disposal.
1.2 Packaging, transport, Storage and characteristic of the installation site
Boxes containing the whole structure, with installation manual and user manual.
Transport is carried out by any road haulage contractor as long as they respect the following characteristics:
Temperature (°C): -15 / +60; Humidity: 10 / 75 %; Atmospheric pressure (h/Pa): 500 / 1060.
The devices packaged must be stored (warehoused) in a dry place and at the following temperature:
Temperature (°C): +10 / +40; Humidity: 10 / 75 %; Atmospheric pressure (h/Pa): 500 / 1060.
The site appointed for the installation of the equipment must have the following characteristics:
Temperature (°C): +10 / +40; Humidity: 30 / 75 %; Atmospheric pressure (h/Pa): 700 / 1060.
1.3 Graphic symbols used on the Product and packaging
Description symbols present on labels, on product, and manual:
Graphic symbol proving the CE marking
of the product
RECYCLING! Product must be recycled
separately
Symbol indicating the manufacture date
(month and year)
B-Type device. Indicates the level of
protection against direct and indirect
contact
Consult accompanying document
Attention
Address of the Manufacturer
Maximum number of packages stackable
Maximum number of packages stackable
Breakable package

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1.4 Declaration of Conformity of the Manufacturer
The company:
RIMSA P. LONGONI S.r.l. Via Monterosa, 18/20/22 - 20831 SEREGNO (MB) - ITALY
Declares under its own responsibility that the Product (Medical lighting device for surgical and diagnosis use):
made by RIMSA P.LONGONI S.r.l., complies with Annex VII of Directive 93/42/EEC dated 14/05/1993, and
subsequent amendments (including Directive 2007/47/EC dated 05/09/2007) and the following standards:
IEC 60601-1
(Part 1: General requirements for basic safety and essential performance)
IEC 60601-2-41
(Part 2: Particular requirements for basic safety and essential performance of surgical luminaires
and luminaires for diagnosis)
IEC 60601-1-2
(Part 1: General requirements for basic safety and essential performance –Collateral standard:
Electromagnetic compatibility –Requierements and tests)
Classification with reference to article 9 and Annex IX of Directives 93/42/EEC and 2007/47/EC
DURATION:
Short term (Par.1 “Definitions”, art.1, sub-section 1.1, annex IX)
DESCRIPTION:
Non-invasive medical device (Par.1 “Definitions”, art.1, sub-section 1.2, annex IX)
Active medical device (Par.1 “Definitions”, art.1, sub-section 1.4, annex IX)
CLASS:
I (Par.3 “Classification”, art.1, sub-section 1.1 Rule 1, annex IX)
Reference to technical file Code RIM-FT019.
The conformity assessment is developed with reference to article 11 of Directive 93/42/EEC and 2007/47/EC.
The RIMSA Quality System complies with UNI EN ISO 9001 and UNI CEI EN ISO 13485 standards and is
certified by CSQ (CSQ certificate no. 9120.RMS1 and 9124.RMS2).
The Medical Device to illuminate the body of the patient locally is supplied in NOT STERILIZED form.
Name: Paolo Longoni
Position: Managing Director
PRIMALED/ PRIMALED-FLEX
APPLICARE
ETICHETTA

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1.5 Warranty Certificate
1. The appliance is covered by an 18-month warranty, including electrical parts.
2. The warranty begins on the date of product shipment from the GIMA warehouse to the buyer.
3. In case of disputes, the date indicated on the “transport document” attached to the goods shall be deemed valid.
4. The warranty only covers the sending of Product spare parts to the buyer or, in the event of GIMA considering
the replacement of spare parts not feasible, the replacement of the entire product, after fabrication faults have
been properly ascertained at the undisputable judgement of GIMA. The warranty does not therefore cover any
other costs or expenses (including, by way of example but without limitation, labour costs, packaging costs and
transport costs, etc.).
5. The guarantee does not include the components subject to normal wear, such as halogen bulbs, LEDs, fuses,
relays, ball bearings, etc.
6. The warranty does not cover:
- malfunctions due to failure to comply with the instruction manuals;
- malfunctions due to installation and/or maintenance errors;
- malfunctions or faults caused by carelessness, negligence, incorrect use or other causes not attributable to
GIMA;
- malfunctions or faults due to the fact that the electrical system of the premises where the machine is
installed is not in compliance with International or local standards for electrical systems in premises used for
medical purposes and similar standards.
7. GIMA shall repay direct damages suffered by the buyer and which are documented as attributable to its product,
caused within the warranty period, for an amount not above 40% of the net value of the product as indicated on
the buyer’s invoice. GIMA’s liability is expressly ruled out for indirect damages or consequential damages
(including cases of the lamp not being used) deriving from the supply.
8. This warranty certificate replaces legal warranties for faults and non-conformities and rules out any other
possible liability of GIMA originating from the supplied products.
9. The payment of any damages to persons or things due to product malfunction or faults shall be limited to the
maximum amount of GIMA’s insurance coverage for civil liability.
10.The warranty shall be automatically invalidated in the event of:
-the product having been tampered with or modified by the buyer or third parties;
-the product having been repaired by the buyer or third parties, without following the instructions in the
instruction manuals;
-the product serial number having been cancelled, defaced or removed;
-the buyer not being up to date with payments.
11.For jobs to be done under warranty, the buyer shall contact GIMA only.
12.The component parts replaced under warranty must only be returned to GIMA, if so requested by GIMA,
carriage free and suitably packed.
13.In case of failure to return a part requested by GIMA, the cost of the component part will be charged.
14.GIMA cannot accept returns from end users or in any case from parties other than the buyer.
15.Products returned to GIMA must be complete with documentation authorising such return and another document
describing the malfunction.
16.For everything not indicated on this warranty certificate, reference shall be made to the laws of Italy.
17.For all disputes deriving from or related to the orders to which this warranty certificate applies and which cannot
be amicably settled between the parties, the only competent law court shall be that of Milan.

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2. Product Installation
Before installing the Product, make sure that all the packages are present and in good condition, without any
transport-related damage, and that the contents correspond to what is specified above.
Claims will be considered only if the seller or the forwarder are informed immediately. Each claim must be
in writing. Goods are always carried at the buyer’s risk.
Keep the original package in case the lamp must be sent back.
2.1 Installation mobile version
1. Insert the lamp into the upper hole of the pipe.
2. Screw down the knob, taking care of the thread
3. Connect the power cable plug to the network line (please check that the network line is
equipped with the ground cable).
2.2 Installation wall version (S/12 MED fixing)
1. Fix the clamp S/12 MED on the wall using 3 expansion screws.
2. Insert the lamp into the upper hole of the wall clamp S/12MED.
3. Follow points 2 and 3 of paragraph 2.1.
2.3 Installation wall version (rail bar fixing)
1. Fix the rail bar supports using 2 expansion screws.
2. Put the clamp on the bar and tighten the handle.
3. Insert the lamp into the upper hole of the rail clamp
4. Follow points 2 and 3 of paragraph 2.1.
2.4 Installation table version (S11 fixing)
1. Fix the clamp S/11 to the table tighten the screwed pivot.
2. Insert the lamp into the upper hole of the table clamp
3. Screw, using a screwdriver, the screw on the back of the clamp,
4. Follow point 3 of paragraph 2.1.
2.5 First starting
At this point is possible to power the Product to check its correct functioning.
Follow the steps below:
1- Press the green switch of the base;
2- Press the I/O keyboard on the front side of the reflector.
2.6 Installation verification and Product testing operations before use
The following prescriptions are to be considered compulsory during verification of the installation, since they prove
the correct execution of all the points set out. For such reason it is necessary to tick each point when it is treated.
1. Check the suitability of the wall to the installation of the Product.
2. Check the right installation of the pivot into the clamp/stem
3. Make sure the movement mechanism works perfectly. Check the mechanical operation of the Product
by directing and rotating
4. After turning on the Product, it must emit light from the reflector
Seal and signature of the installer:

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3. Importance of personal safety
3.1 Intended use
The Product is made to light up the area occupied by the patient undergoing diagnostic or observation, and has
been designed for use in medical surgeries.
The Product correctly lights up the field of work from a minimum distance of 40cm to a maximum distance of
70cm from the point of light emission.
The Product, in compliance with the standard IEC 60601-2-41, is assesses as luminaire for diagnosis:
-Luminaire to illuminate the body of the patient locally in order to support diagnosis or treatment which could
be interrupted without any hazard for the patient in case of failure of the light. (Is not intended to be used in
operating rooms)
3.2 Enviromental conditions
-The Product is not suitable for use in explosion-risk areas.
-The Product is not suitable for use in the presence of inflammable mixtures of anaesthetics with air, oxygen or
NO2(laughing gas).
-During operation, the ambient temperature must be between 10°C and 40°C.
-Relative humidity must be between 30% and 75%.
-Atmospheric pressure must be between 700 and 1060hPa.
3.3 Other secondary conditions (secondary effects)
-Do not direct the light source into the patient’s and/or operator’s eyes.
-Obligation to adequately protect the patient’s eyes.
Failure to follow such precautions could cause glare and potential damage to the retina.
-Never place and/or hang anything on the Product.
Unless this precaution is taken, positioning will not be reliable and the danger exists of such objects falling in
the operating area.
-Never hang on the Product with the body weight of a person.
Unless this precaution is taken, mechanical parts of the Product could be damaged.
-Never cover the head of the Product during operation.
Failure to comply could prevent heat exchange with the environment and the Product could overheat.
-Avoid knocking the rocker arms and Product head.
A violent knock could damage the Product and pieces of paint could chip off and fall onto the operating field in
the patient area.
4. Description of the operations
The membrane keyboard is fitted to the light head and grants the following functions:
-On/off switch by means of the membrane key I/O (1)
-Light intensity adjustment by pressing the keys (2) and (3), with display of intensity reached by means of 3
green position micro LEDs
-Colour temperature selection by pressing the key with the letter “K” (3) while the set value is displayed by
means of the lighting up of one of the 2 green micro LEDs
-Courtesy light selection by pressing the key with the letter “C”, three leds without lens offer a soft light not
suitable for examination (5). Courtesy light is available only when lamp is switched-off, it can be adjusted the
light intensity but not the color temperature. Press key I/O (1) to have the standard functioning.
The light field is not adjustable.
2
3
4
5
1

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5. Cleaning and disinfection
5.1 Cleaning the Product
Switch the Product off by means of the operating theatre main switch and make sure it cannot be switched back on.
Protect the Product against water spray and do not clean it/disinfect it with liquids.
Leave the lamp body to cool down. Only clean the lamp body when it is cold.
Clean with appropriate detergent with low alkaline content and chlorine free.
Do not use abrasive products, petrol, paint thinners, alkaline detergents, acids, containing alcohol or aldehydes;
Dose the detergents so no liquids penetrate into the lamp bodies and into the support arm system.
Clean the Product with a damp but not wet cloth.
5.2 Disinfecting
Switch the Product off by means of the operating theatre main switch and make sure it cannot be switched back on.
Protect the Product against water spray and do not clean it/disinfect it with liquids.
Leave the lamp body to cool down. Only disinfect the lamp body when it is cold.
Disinfectants can contain substances which are harmful for the health: only use disinfectants in accordance with the
rules on hygiene established by the hospital.
The Product operator must comply with the rules established by the national commission for hygiene and
disinfection.
To prevent damaging parts in stainless steel or aluminum, only use disinfectants which are chlorine and halogen
free.
To prevent the plastic parts becoming fragile, use only disinfectants with low alcohol content.
Dose the disinfectants so no liquids penetrate inside the lamp bodies and into the support arm system.
Clean the Product with a damp but not wet cloth.
5.3 Sterilizing the handpieces
Replace the handpieces as soon as these become cracked or deformed, as these could fall in the wound area.
The Product operator must comply with the rules of the national commission for hygiene and disinfection.
Handpiece fitting / removal:
- rotate counter clockwise the handpiece for remove it.
- rotate clockwise the handpiece, until it to beat the head lamp and the rotation result impossible.
Cleaning, disinfecting and sterilizing the handpiece:
The handpieces are made of plastic material resistant to heat and knocks (PPSU).
They can be cleaned with a neutral or lightly-alkaline detergent free of active chlorine.
To disinfect the handpieces, we suggest using alcohol or aldehyde-based products. The disinfectants must be
approved by the manufacturer for use on polyphenylsulfone (PPSU).
Before sterilizing, rinse the handpieces.
The handpieces can withstand about 300 steam sterilization cycles as follows:
-steam sterilization at 121°C 1.3bar from 25 to 30 minutes,
or
-steam sterilization at 134°C 2.3 bar for 4 minutes.
Position the handpieces straight with open side downwards.
Do not exceed a sterilization temperature of 134°C.
Avoid the handpieces coming into contact with other objects during the sterilizing process.
Each Product, over time, is subject to a certain amount of wear. Product safety and operation must therefore
be checked during inspection and maintenance intervals.

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6. Adjustments
6.1 Yearly inspections by the operator
Keep to the yearly inspection schedules and inspect the product according to IEC 62353 standard.
6.2 Repairs
The Product must only be opened and repaired by a technician who has attended a course on the Product organised
by the manufacturer or by a qualified technician in possession of the necessary technical skills.
6.3 Adjustments
The Product is sold already balanced and does not require further adjustment. In the event, In the event of the
Product becoming stiff or loose over time, please contact the service center.
6.4 Troubleshooting
n
Problem
Solution
1
The Product does not switch on
Check the INPUT and OUTPUT (24V) power supply voltage and
the voltage of the electronic board terminal (24V).
2
The Product does not remain in position
See the attached instructions
3
The light flickers
Contact the service center
4
The light beam on the operating field is
not focalized
Contact the service center
6.5 Routine maintenance
n
Period
Job
1
Once a year
Inspect all the lamp joints and make sure they are not hard to move. If Product does not
maintain the position or is hard in movements, see the attached.
2
Once a year
Make sure the retention screws are tightened properly. If these are not properly fastened,
adequately tighten.
3
Once a year
Check the condition of the Product paint. Make sure there are no paint pieces that could
fall on the operating field.
6.6 Spare parts list
Description
Order code
Sterilizable handle
Z100848
Electronic board
Z300640
Electronic card
Z300231

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7. Technical data
Technical data
PRIMALED/ PRIMALED-FLEX
Illumination Ec at a distance of 50cm [Lux] ± 10%
80.000 / 86.000
Color temperature (±5%) [K]
4.500 / 5.000
Color rendering index Ra [-]
95
Maximum Irradiation [W/m2]
225
Irradiation / Illuminamtion [mW/m2lx]
2,8
Maximum irradiation in the UV [W/m2]
0,001
Focus by handle
No
Data on electrical connection
Primary alternating voltage [Volt ac]
100-240
Frequency [Hz]
50-60
Absorbed power [VA]
30
Light source
N°12 Led x 1.4W
LED light source duration [h]
(this datum can vary according to voltage peaks and the
frequency of use)
50.000
Light intensity control [%]
25 –100
General data
Color
RAL 9003
Directive
93/42/EEC (included 2007/47/EC)
Standard
EN 60601-2-41
Electrical safety class
Class I
Protection against direct and indirect contacts
B-type device
Dimensions
Lamp body diameter [cm]
19,5
Diameter of the poly-elliptical reflector [cm]
3,2
Light emission surface [cm2]
65
Lamp weight (Primaled / Primaled-Flex) [Kg]
3,5 / 3,3
Certificate
Complying with directive 93/42/EEC
(included 2007/47/EC)

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8. Electrical diagram

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9. EMC declaration
The Product has been tested in accordance to EN60601-1-2 to ensure proper electromagnetic compatibility.
Portable and mobile RF-communications equipment can affect the Product. Other products used in the vicinity of
Product should also comply with this standard.
The Product is intended for use in the electromagnetic environment specified below. The customer or the user of
the Product should assure that these are used in such an environment.
Emissions test
Compliance
Electromagnetic environment-guidance
RF emissions
CISPR 11
Group 1
The Product uses RF energy only for its internal
function. Therefore, its RF emissions are very low
and are not likely to cause any interference in nearby
electronic equipment.
RF emissions
CISPR 11
Class A
The Product is suitable for use in all establishments
other than domestic, and may be used in domestic
establishments and those directly connected to the
public low-voltage power supply network that
supplies buildings used for domestic purposes,
provided the following warning is heeded:
Warning: This equipment/system is intended for
use by healthcare professionals only. This
equipment/system may cause radio interference or
may disrupt the operation of nearby equipment. It
may be necessary to take mitigation measures, such
as re-orienting or relocating the Product or shielding
the location
Harmonic emissions
IEC 61000-3-2
Class A
Voltage fluctuations/
flicker emissions
IEC 61000-3-3
Compliance
Immunity test
IEC 60601-1-2
test level
Compliance level
Electromagnetic environment-
guidance
Electrostatic discharge
(ESD)
IEC 61000-4-2
+/- 6 kV contact
+/- 8 kV air
+/- 6 kV contact
+/- 8 kV air
Floors should be wood, concrete
or ceramic tile.
If floors are covered with
synthetic material, the relative
humidity should be at least 30%
Electrical fast transient /
burst IEC 61000-4-4
+/- 2 kV
for power supply unit
+/- 1 kV
for input/output lines
+/- 2 kV
for power supply
lines
+/- 1 kV
for input/output lines
Mains power quality should be
that of a typical commercial or
residential environment.
Surge
IEC 61000-4-5
+/- 1 kV
differential mode
+/- 2 kV
common mode
+/- 1 kV
differential mode
+/- 2 kV
common mode
Mains power quality should be
that of a typical commercial or
hospital environment.

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Voltage dips, short
interruptions and voltage
variations on power
supply input lines
IEC 61000-4-11
<5% UT
(>95% dip in UT)
For 0,5 cycle
40% of UT
(60% dip in UT)
For 5 cycles
70% of UT
(30% dip in UT)
For 25 cycles
<5% UT
(>95% dip in UT)
For 5 sec
<5% UT
(>95% dip in UT)
For 0,5 cycle
40% of UT
(60% dip in UT)
For 5 cycles
70% of UT
(30% dip in UT)
For 25 cycles
<5% UT
(>95% dip in UT)
For 5 sec
Mains power quality should be
that of a typical commercial or
hospital environment. If the user
of the Product requires continued
operation during power mains
interruptions, it is recommended
that the Product be powered from
an uninterruptible power supply
or battery.
Power frequency
(50/60Hz) magnetic
field
IEC 61000-4-8
3 A/m
3 A/m
Power frequency magnetic fields
should be at levels characteristic
of a typical location in a typical
commercial or hospital
environment.
NOTE UTis the a.c. main voltage prior to application of the test level.
Immunity test
IEC 60601 test level
Compliance
level
Electromagnetic environment-
guidance
Conducted RF
IEC 61000-4-6
Radiated RF
IEC 61000-4-3
3 Vrms
150 kHz to 80 MHz
3 V/m
80 MHz to 2,5GHz
3 Vrms
3 V/m
Portable and mobile RF
communications equipment should be
used no closer to any part of the
Product, included cables, than the
recommended separation distance
calculated from the equation applicable
to the frequency of the transmitter.
Recommended separation distance
d = 1,2√P 150 KHz to 80 MHz
d = 1,2√P 80 MHz to 800 MHz
d = 2,3√P 80 MHz to 2,5 GHz
where P is the maximum output power
rating of the transmitter in watts (W)
according to the transmitter
manufacture and dis the recommended
separation distance in meters (m).
Field strengths from fixed transmitters,
as determined by an electromagnetic
site survey, should be less than the
compliance leave in each frequency
range.
Interference may occur in the vicinity of
equipment marked with the following
symbol.

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Recommended separation distance between
portable an mobile RF communications equipment and the Product
The Product is intended for use in an electromagnetic environment in which radiated RF disturbances are
controlled. The customer or the user of the Product can help prevent electromagnetic interference by
maintaining a minimum distance between portable and mobile RF communications equipment (transmitters)
and the Product as recommended below, according to the maximum output power of the communications
equipment.
Rated maximum output
power of transmitter
W
Separation distance according to frequency of transmitter
m
150 kHz to 80 MHz
d = 1,2√P
80 MHz to 800 MHz
d = 1,2√P
800 MHz to 2.5 GHz
d = 2,3√P
0.01
0.12
0.12
0.24
0.1
0.38
0.38
0.73
1
1.2
1.2
2.3
10
3.8
3.8
7.3
100
12
12
23
For transmitters rated at a maximum output power not listed above, the recommended separation distance din
meters (m) can be estimated using the equation applicable to the frequency of the transmitter, where P is the
maximum output power rating of the transmitter in watts (W) according to the transmitter manufacturer.
Note 1: at 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by absorption
and reflection from structures, objects an people.

Operative Manual
MO079-IT
15/06/12
Rev.0
Pag. 15 di 16
10. Friction regulation
The device is provided already balanced and no further adjustments are required; however, if over time the
movement of arms around their rotation joints should became too rigid or too soft, so as to not allow the
maintenance in position of the device itself, it is possible to act on the different friction systems in order to
restore the correct balance.
Use the included Allen key to adjust the friction force in correspondence of rotational joints and, therefore, the
consequent movement of movable arms.
ROTATION JOINTS
Depending on the version of the device, there is a different number of joints and so of frictions:
FRICTION ADJUSTING PROCEDURE
In correspondence of the joint of interest,
using the Allen key, act on the regulating
screw on the side of joint.
Rotate clockwise to increase the force of
friction and hence stiffen the movement.
Rotate counter-clockwise to decrease the
friction force and make lighter the movement.
After the adjustment the movement must be
fluid and homogeneous.
Table version
Table version with flexible arm

Operative Manual
MO079-IT
15/06/12
Rev.0
Pag. 16 di 16
Note