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DEAR CUSTOMER THANK YOU FOR CHOOSING A GLOBUS PRODUCT. WE REMAIN AT YOUR ENTIRE DISPOSAL FOR ANY ASSISTENCE OR ADVICE YOU MAY NEED Pysiolaser 1000 Physiolaser 500 The lasertherapy devices (Pysiolaser 1000 e Pysiolaser 500) are produced and distributed by: DOMINO s.r.l.
Table of contents TECHNICAL FEATURES ..........................6 Device ............................... 6 Use conditions ............................6 Technical features of the laser ........................ 6 Accessories ............................... 7 EQUIPMENT ..............................8 CONNECTIONS ............................9 Device ............................... 9 Handpiece Laser ............................9 Battery: how to charge the batteries ..................... 9 LABELLING AND SYMBOLS ........................
Medical Device of II b class Laser of IV Class Nominal power (CEI EN 60825-1): Up to1000mW Beam divergence: 13° Power Density: up to 1 W/cm2 max (Physiolaser 1000) 500mW/cm2 max (Physiolaser 500) NOHD: 0.27 m (1W) 0.18 m (500mW) Spot size: 3.5 mm or 11.5 mm...
Accessories Glasses for the patient (Physiolaser 1000) Visual field PPE: >40 Length regulation and sidepiece inclination: jerky mechanism Ventilation system: small holes in the lateral protections Complete PPE weight: 34 Materials: polycarbonate VLT%: 0,36 Color: green 7 Bend: Basic 6...
EQUIPMENT A: CARRYING CASE B: GLASSES FOR THE OPERATOR C: GLASSES FOR THE PATIENT D: WARRANTY E: POWER SUPPLY UNIT F: LASER HANDPIECE G: DEVICE The device is supplied complete of laser handpiece, power supply unit, glasses for the operator and glasses for the patient; opening the package, it is necessary to check that the basic equipment is complete.
- rehabilitation centers; - general pain treatments (medical treatments); - for beauty and sport purposes. CONNECTIONS Device Power supply by electricity grid The Physiolaser operates connected to the mains. To connect the power supply unit to the connector, plug it as shown below. Handpiece Laser To connect the cable of the handpiece to the device plug it into the appropriate inlet removing the sticker with the yellow symbol (see picture).
LABELLING AND SYMBOLS Warning This symbol on your device indicates that it complies with the directives on medical devices (93/42/CEE 47/2007CEE). The number of the notified unit is 0476. It indicates that this is a I class device. ...
It refers to the production lot It refers to the percentage of storage humidity It refers to the manufacturing date It refers to the interruption of the laser emission Attention danger laser emission not visible It identifies the risks related to the laser use and it classifies them Mains voltage PRI ...
Panel and keyboard ON/OFF/OK Button (To turn on/off and confirm the treatment) LEFT/BACK Button P+ Button (to scroll the programs up) P- Button (to scroll the programs down) RIGHT Button Up/Down left button to modify the power Fn button to activate some special functions described in the “instructions for use” Display/Interface 12 ...
ALARMS Compliance Certifications: CE MDD Certificate The sound and acoustic signals are in compliance with the directive 60601-1-8. Meaning Correct power emission: the treatment proceeds correctly, the laser emission is present. Cable not connected Verify that the cable is connected to the right output. Device in pause.
-The unit should be used only with the laser handpiece provided originally (or Globus branded) and according to the therapeutic modalities described. - Before each use always check the integrity of the unit. This is a fundamental requirement for carrying out therapies, do not use the unit if either the buttons or cables are defective or malfunctioning.
- it must be used following the indications and under the physician or physiotherapist’s control. - it must be kept out of the reach of children. - if there is any health problem, it must be used only after seeing a doctor; - once you have turned on the device, make sure that in the display the software version and the model of the device appear, it means that the device is working and it is ready to be used.
Contraindications Do not use the lasertherapy in the following cases: - Do not carry out this treatment on pregnant women. - On children under 15. - Do not point the laser on big moles or on dark areas that could absorb excessive quantity of energy.
Battery Battery info. The device is equipped with a menu that can visualize the charge of the battery, the values and the conditions of the end of the charge. It is recommended to access to this menu only after a complete charge of the batteries.
INSTRUCTIONS FOR USE Pin unlocking The device, when not used, should be protected against a not authorized use. The PIN function has this objective; it consists of a SW code intended to impede the device use to not authorized staff. For a correct connection of the product it is necessary to proceed as follow: Connect the handpiece to the relative output of the device;...
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Phototype setting Light (A) Dark (B) By choosing the phototype B, the emission intensity will be automatically reduced and the duration of the treatment will be increased, both of 20 %. Light phototype= for light/normal skin Dark photype= for dark skins or dark marks. How to start the program After selecting the program, the display will show the message “ready”.
Visualization during a program execution Dosage per Wave length of the laser beam Phototype Handpiece emission Intensity Total Treatment dosage duration Visualization of the parameters during the execution By holding the * button, the screen will show you the visualization normally characterizing a lasertherapy protocol. The following screen with the specific values of the ongoing program will appear: ...
How to change the working phase parameters After starting the program, the power of the treatment can be modified by using the P+ and P- buttons. By increasing or decreasing the power, the duration of the treatment will change. Special Functions “Last 10” Function The device stores the last 10 executed programs, so that these are available for a rapid and easy execution.
The "Programming" function The “Programming” function is activated only when the laser pointer is connected. The device offers the possibility to create/modify new programs. This makes the device flexible and adaptable to all users' requirements. From the "Programming" entry of the main menu, it is possible to create new programs (when the message EMPTY appears) and to execute already personalized programs.
Duty cycle SPOT Diamater Emitted energy Dosage Remaining Frequency Intensity Treatment area time of the program By using the Up and Down buttons you can modify the frequency (only in pulsed mode), the program duration, the intensity and the size of the area to be treated, and you can combine these parameters in order to have the desired protocol.
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By pressing the * button you can visualize and modify the information “E/p” Energy per point or the information “D (dosage) in J/cm²”. This allows the operator to choose the parameter he wants to set. How to modify a program Inside the Programming menu, select the program number you wish to modify...
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Language selection FUNCTION The "Language Selection" function in the setup menu permits to choose among 4 different languages for the navigation using the UP and DOWN buttons. Confirm the selection with OK. Warning sounds FUNCTION The "Warning sounds" function in the setup menu permits to enable (ON) or disable (OFF) the acoustic tones emitted by the unit.
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APPLICATION MODE: THERAPEUTIC AND BEAUTY EFFECTS The biological changes caused by the laser light, determine the following effects: 1) Biostimulating effect. The biostimulating effect of the laser accelerates the cicatrization of ulcers and sores. The laser light stimulates the mitochondris and accelerates the ATP production. The increased production of APT recharges the cells of energy so that, if the cells are damaged because of inflammatory, traumatic or regenerative causes, they restart to execute their physiological functions.
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MAIN AREAS TO BE TREATED SHOULDER PAIN ANKLE SPRAIN KNEE ARTHROSIS/OSTEOARTHRITIS FINGER PAIN ACHILLES TENDON INFLAM. EPICONDILYTIS BACK PAIN WITH RADICULOPATHIES NECK PAIN CARPAL TUNNEL TEMPORO/MANDIBULAR PAIN 27 ...
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Program list HEALTH- REHABILIATION In compliance with the last regulations of the Ministry of Health, medical treatments are indicated in the below list The following programs are medical Health Physiolaser Physiolaser Session/ # weeks Ø Spot 1000 week Arthrosis 11,5 Ankle sprain 11,5 Knee pain...
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Program list BEAUTY – FITNESS (non medical treatments) X = Available program Beauty Physiolaser 500 Physiolaser 1000 FACE BEAUTY Wrinkles x x Acne x x Dehydrated skin x Skin rejuvenation x x Skin – face lifting x ...
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WARRANTY CONDITIONS The device is guaranteed to the first user for a period of twenty-four (24) months from the date of purchase against defects in materials or of the manufacturing, provided that it is used properly and maintained under normal operating conditions.
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Il cliente o l’utilizzatore del PHYSIOLASER 1000 deve garantire che esso viene usato in tale ambiente. The PHYSIOLASER 1000 is intended for use in the electromagnetic environment specified below. The customer or the user of the PHYSIOLASER 1000 should assure that it is used in such an environment. Prova di emissione Conformità...
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Il cliente o l’utilizzatore del PHYSIOLASER 1000 deve garantire che esso viene usato in tale ambiente. The PHYSIOLASER 1000 is intended for use in the electromagnetic environment specified below. The customer or the user of the PHYSIOLASER 1000 should assure that it is used in such an environment. Prova di immunità...
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5 cicli_cycles per_for 5 hospital environment. If the user cicli_cycles IEC 61000-4-11 of the PHYSIOLASER 1000 requires continued operation 70% U during power mains interruptions, 70% U (30% buco in_dip in it is recommended that the...
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Il cliente o l’utilizzatore del PHYSIOLASER 1000 deve garantire che esso venga usato in tale ambiente. The PHYSIOLASER 1000 is intended for use in the electromagnetic environment specified below. The customer or the user of the PHYSIOLASER 1000 should assure that it is used in such an environment. Prova di immunità...
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150 kHz to 80 MHz 80 MHz to 800 MHz RF irradiata 3 V/m da 800 MHz a 2,5 GHz Radiated RF 3 V/m 800 MHz to 2,5 GHz IEC 61000-4-3 da 80 MHz a 2,5 80MHz to 2,5 GHz ove P è...
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RF fissi, si dovrebbe considerare un’indagine elettromagnetica del sito. Se l’intensità di campo misurata nel luogo in cui si usa un PHYSIOLASER 1000, supera il livello di conformità applicabile di cui sopra, si dovrebbe porre sotto osservazione il funzionamento normale del PHYSIOLASER 1000. Se si notano prestazioni anormali, possono essere necessarie misure aggiuntive come un diverso orientamento o posizione del PHYSIOLASER 1000.
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RF COMMUNICATIONS EQUIPMENT AND THE PHYSIOLASER 1000 FOR EQUIPMENT AND SYSTEM THAT ARE NOT LIFE-SUPPORTING Il PHYSIOLASER 1000 è previsto per funzionare in un ambiente elettromagnetico in cui sono sotto controllo i disturbi irradiati RF. Il cliente o l’operatore del PHYSIOLASER 1000 possono...
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