MNPG52-06 (MAG2000 ENG) - I
Contents
1. Attention it s possible to stop temporary the therapy at any time pressing OK key at least for 2 seconds Press again OK key to continue the treatment During pause time green led turns off till the treatment restarts Attention it s possible to get out from the treatment at any time by i ci pressing once key screen will display the base setting step 6 By _ pressing again key screen will display programs menu step 5 Attention MAG2000 recognizes applicators correct connection During the treatment screen displays connection state under the magnet icon The presence of symbol nex to the channel number 1 or 2 indicates correct connection and applicator recognition The symbol X near to the channel number 1 or 2 indicates a not correct connection of applicator or its absence or even its incorrect functioning see Functioning control paragraph Stored programs list Pre adjusted values Recommended values Pathology Treatment Treatment cycles interval Epicondyits 45 2 6 20 24 hours _ 10 Epitrocieiis s 2 6 20 24hours _ I A C E R Srl 21 MNPG52 06 n TOT contusions 12 Lumbalgy e Da 1 shoulderarthrosis 30 2 6 15 24hours 15 nee arthrosis 45 2 6 20 24hours 16 periarthritis 50 2 6 20 24hours 17 coxarthrosis 50 2 6 20 24hours 18 muscular atrophy 35 2 6 20 24hours o e a e ato contracture 20 osteonecrosis 5o 22. Do not wear metallic objects during therapy Take care to place the green side of the therapeutic belt on the skin Use only cables and applicators supplied by the Manufacturer Inadequate cables and applicators could damage the device and or could be hazardous for the patient The user must periodically verify cables and applicators insulation and control their integrity eventually by contacting the manufacturer Pay attention to use belt connection cables and power supply strangulation danger Pay attention when the cables are next to the patient neck and head in this case it is recommended to keep a safe position and to avoid sudden movements that could twist the cables The materials used for the device production had passed the toxicity regulations In case of allergic reactions please suspend the treatment and consult a doctor Do not use on irritated skin or on open wound Do not connect the device and its accessories to other devices not mentioned in the present user manual Keep it out of children and animal s reach Avoid the device and accessories exposition to excessive direct sunlight and dust Make reference to Maintenance paragraph I A C E R Srl 11 MNPG52 06 _ h MEDICAL DIVISION e n case of prolonged treatments even up to 8 hours we suggest to use intensity lower than 50 for all programs In this case the efficacy is given by the prolonged treatment time rather than maximum adjustable intensity
3. Italy Certification Path Annex II excluded point 4 MAG2000 is a Class Ila equipment with reference to Directive 93 42 EEC MDD annex IX rule 9 and following modifications Martellago 06 03 13 Legal Rappresentative Mario Caprara dI I A C E R Srl 5 MNPG52 06 FER MEDICAL DIVISION Specifications MAG 2000 has the following specifications e Class lla equipment Directive 93 42 CEE Annexed IX rule 9 and following modifications e Class II applied part type BF Classif CEI EN 60601 1 e P21 protection equipment against solids dust and liquids penetration e Equipment and accessories not subjected to sterilization e Use of the equipment is prohibited close to flammable substances when mixed with air with nitrous oxide or when mixed with any flammable agents and in environments with high concentrations of oxygen e Continuous operating mode equipment e Equipment not suited to be used in external Purpose Clinical purpose Therapeutic Use Clinic Hospital and domestic use MAG2000 is indicated for the treatment rehabilitation and functional recovery of the following pathologies e wrist hand shoulder foot ankle and knee articulation e skeletal motor apparatus e arthrosis e atrophies and muscular dystrophy e bursitis e bruises I A C E R Srl 6 MNPG52 06 NL MEDICAL DIVISION e degeneration of locomotor apparatus e sprains e periarthritis e benign lesions and
4. 2000 is intended for use in the electromagnetic environment specified below The customer or the user of MAG 2000 should assure that is used in such environment Immunity test Test level EN Compliance level 60601 1 2 6kV contact 8kV air Electrostatic discharge ESD EN 61000 4 2 6kV contact 8kV air Electrical fast transient burst IEC 61000 4 4 2kV for power supply lines I A C E R Srl 27 2kV per power supply lines Electromagnetic environment guidance Floors should be wood concrete or ceramic tile If floor are covered with synthetic material the relative humidity should be at least 30 Mains power quality should be at that of a typical commercial or hospital environment MNPG52 06 Impulses 1kV differential 1kV differential Mains power quality EN 61000 4 5 mode mode should be at that of a typical commercial or hospital environment Voltage dips short lt 5 Ur lt 5 Ur Mains power quality interruptions and gt 95 dips of Ur gt 95 dips of Ur should be at that of voltage variations on per 0 5 cycles per 0 5 cycles a typical commercial power supply input Or hospital lines 40 Ur 40 Ur environment IEC 61000 4 11 60 dips of Ur 60 dips of Ur If the user of the per 5 cycles per 5 cycles MAG2000 requires continued operation 70 Ur 70 Ur during power mains 30 dips of Ur 30 dips of Ur interruptions it is per 25 cycles per 25 cycles recommended that M
5. muscular tears e tendinitis MAG2000 is particularly suitable for the treatment and the care of the osteoporosis and all the pathologies on bony tissues Cellulite treatment is not inserted in the CE0476 marking of the device device Cellulite treatment can be used only for beauty purposes Thanks to its high magnetic field intensity MAG2000 is particularly Suitable for the treatment of bone fractures also with rigid bandages or braces MAG2000 device is indicated both for professional physiotherapists medics etc and for domestic user In case of home therapy we recommend using the device exclusively on medical therapist suggestion According to medical devices directives the fabricant suggests a device control to check its efficiency and safety every 2 years Expected lifetime of the device and its accessories time after which we suggest sending the device to the manufacturer for safety checks 2 years Technical features Power supply Power UE24WCP 150120SPA 15VDC 1 2A Max absorbed current 0 6 A Insulation class CEI EN 60601 1 Il Applied part CEI EN 60601 1 BF Dimensions mm 180x110x50 Field intensity Adjustable on increasing level up to 100 Gauss each channel in P1 P20 programs Adjustable on increasing level up to 150 Gauss each channel in P21 P35 programs Squared wave frequency 1 100 Hz Therapy time Adjustable by user I A C E R Srl 7 MNPG52 06 I TECH MEDICAL DIVISION In frequency programs fr
6. the symbol on the label concerning separate waste collection when disposing this product please use the designed areas for disposing electronic waste or contact the manufacturer Troubleshooting If it is used in accordance with the instructions of the user manual MAG2000 does not need a particular regular maintenance If you find any malfunctioning using MAG2000 please follow these instructions e check the main integrity by connecting a running device to the same main e check the connection with power supply and connection cables integrity e check the correct connection between MAG2000 and the applicator or the applicators e check all the operations have been done properly I A C E R Srl 25 MNPG52 06 f m MEDICAL DIVISION e every two years we suggest a complete check of device contact the manufacturer or locator dealer If you find any problems contact immediately the National Distributor or the manufacturer at the following address A C E R S r l Via S Pertini 24 a 30030 Martellago VE ITALY Tel 39 0415401356 Fax 39 0415402684 www itechmedicaldivision com iacer iacer it Assistance Every intervention on device must be performed by manufacturer For any assistance intervention contact the National Distributor or the manufacturer at the following address ILA C E R S r l Via S Pertini 24 a 30030 Martellago VE ITALY Tel 39 0415401356 Fax 39 0415402684 www
7. walkie talkie can affect the medical device and it s recommended a separation distance d calculated from the fabricant in table R f immunity aspects column 800MHZz 2 5GHz paragraph EMC tables Example for a mobile phone with 2W maximum output power the separation distance d is 3 3 m in I A C E R Srl 12 MNPG52 06 LE 23 B MEDICAL DIVISION order to obtain an immunity level of 3V m or a separation distance d 0 5m for an immunity level of 20V m The device must be installed and commissioned in compliance with the information on electromagnetic compatibility supplied in this manual Also see the EMC Charts paragraph Using accessories transducers and cables other than those specified except for those transducers and cables sold by the manufacturer as spare parts for internal components may result in increased emissions or decreased immunity of the device The device should not be placed next to or on top of other devices Should it prove necessary to place it next to or on top of other devices supervision is essential at all times to control its normal functioning Coniraindications and side effects Patient in pregnancy tuberculosis juvenile diabetes viral in acute phase illnesses mycosis cardiopathic subjects tumours serious arrhythmias or pacemaker carriers children metallic prosthesis carriers acute infections epileptics different medical prescriptions excepted No significant side effects are
8. 6 20 24hours 21 Trein 1 free free 24hours 22 treat 3Hz 3 free free 24hours 23 treat sHz 5 free free 24hours 24 Treat 10Hz 10 free free 24hours 25 treat 15H2 15 free tree 24hours o 26 treat 20H2 20 tree free 24hours 27 treat 30Hz 30 free free 24hours 28 treat 40Hz 40 free free 24hours 29 treat soHz 50 free free 24hours 30 treat 60Hz 6o fre free 24hours 31 treat 7oHz 70 free free 24hours 32 treat 80oHz 80 free free 24hours 33 treat 9oHz 90 fre free 24hours o 34 treat 100Hz 100 fre free 24hours 88 lautoscan 2 6 20 24hours Autoscan program allows to adjust the desired therapy time then it will start automatically a frequency cycle from 10 Hz to 100 Hz with a time therapy of 5 minutes for each frequency It s an ideal program for the regeneration of both hard tissues bones and soft tissues tendons ligaments in the same treatment I A C E R Srl 22 MNPG52 06 le MEDICAL DIVISION Therapy duration values are recommended by I A C E R S r l however the user can adjust the time as he prefers MAG2000 uses therapy time values working frequency values and field intensity values coming from scientific and medical literature as result of well known sperimentations and clinical evaluations Barker Lunt 1983 Bassett Pawluk Pilla 1974 Bassett Valdes Hernandez 1982 Setup langua
9. AG2000 be lt 5 Ur lt 5 Ur powered from an gt 95 dips of Ur gt 95 dips of Ur uninterruptible per 5 seconds per 5 seconds power supply or a battery Mains power 3 A m electromagnetic field EN 61000 4 8 Mains power quality should be at that of a typical commercial Or hospital environment r f immunity MAG 2000 is intended for use in the electromagnetic environment specified below The customer or the user of MAG 2000 should assure that is used in such environment 60601 1 2 level environment guidance EN 61000 4 6 150kHz to 80MHz 150kHz to 80MHz I A C E R Srl 28 MNPG52 06 RF Radiata 3 Veff from 3 Veff from communications equipment EN 61000 4 3 80MHZ to 2 5GHz 80MHz to 2 5GHz should be used no closer to any part of MAG 2000 including cables than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter Recommended separation distance d 1 2 VP 150kHz to 80MHz d 1 2 P 80 MHz to 800 MHz d 2 3 P 800 MHz to 2 5 GHz where P is the maximum output power rating of the transmitter in Watts W according to the transmitter manufacturer and d is the recommended separation distance in metres m Field strangths from fixed RF transmitters are determined by an electromagnetic site survey should be less than the complicance level in each frequency rage Interference may occur in the vicinity of equipment marked with the Co follow
10. USER MANUAL MNPG52 06 Edition 23 04 2014 Magnetotherapy model MAG2000 LA C E R Srl www iacer it www itechmedicaldivision com I A C E R Srl Via S Pertini 24 A 30030 Martellago VE ITALY Tel 39 041 5401356 Fax 39 041 5402684 e mail iacer iacer it http www itechmedicaldivision com Summary Summary 3 Introduction 4 Magnetotherapy 4 Technical Specifications 5 Declaration of conformity 5 Specifications 6 Purpose 6 Technical features 7 Labelling 8 Label details 9 Symbols description 9 Kit contents 10 How to use 11 Warnings 11 Electromagnetic interference 12 Contraindications and side effects 13 Quick use of the device with presetted parameters 13 Adjustable programs instructions 17 Stored programs list 21 Set up language selection 23 Maintenance 23 Functioning control 23 Cleaning 24 Carriage and storage 24 Disposal 25 Troubleshooting 25 Assistance 26 Spare parts 26 EMC tables 2 Warranty 30 I A C E R Srl 3 MNPG52 06 MEDICAL DIVISION Introduction Magnetotherapy It s a long time that low frequency and high intensity pulsed electromagnetic fields have met maximum scientific consent in chronic and degenerative diseases treatment Magnetotherapy uses low frequency and high intensity pulsed electromagnetic fields induced by electric current on a bobbin due to its characteristics the electromagnetotherapy is universally recognized as the most suitable technique for the treatmen
11. ates that therapy is running 9 At the end of therapy the screen will display automatically the menu programs Attention it s possible to stop temporary the therapy at any time pressing OK key at least for 2 seconds Press again OK key to continue the treatment During pause time green led turns off till the treatment restarts Attention it s possible to get out from the treatment at any time pressing once key screen will display the base setting step 6 By _ pressing again key screen will display the programs menu step 5 Attention MAG2000 recognizes applicators correct connection During the treatment screen displays connection state under the magnet icon The presence of symbol nea to the channel number 1 or 2 is an indicator of correct connection and applicator recognition The symbol X near to the channel number 1 or 2 indicates a not correct connection of applicator or its absence or even its incorrect functioning see Functioning control paragraph Therapeutic belt and solenoids couple positioning Here below a list of main positions for the therapeutic belt and for the solenoids couple I A C E R Srl 15 MNPG52 06 I TECH Wrap the belt around the area to be treated or position the belt on the area for example in vertebral column treatment During this phase take care to place the green side of the therapeutic belt on the skin The professional solenoids couple have to be placed in opposit
12. ction The PVC envelope guarantees the IP01 level protection The IP21 protection is guaranteed only when using the device inside the PVC envelope Only domestic use Not protected against liquids entrance keep dry Kit contents MAG2000 contains e NI MAG2000 device N 4 power supply cable 1 5 m N1 user and maintenance manual N1 elastic therapeutic belt with 3 solenoids cable 1 5 m N1 carriage bag NI PVC envelope Solenoids couple magnetotherapy carpet and OSTEOMAT mattress are available as accessory on demand Visit website www itechmedicaldivision com to obtain more information I A C E R Srl 10 MNPG52 06 MEDICAL DIVISION How to use Wamings Please read carefully the user manual before using MAG2000 We recommend to visit magnetotherapy section on website www itechmedicaldivision com in order to obtain other information Take care of what follows Take care of position and meaning of the labels on MAG2000 Do not damage the therapeutic belt acting on connection cable and avoid to roll up the cable around the belt or the device Check the integrity of the power supply before use Avoid the use in case of damage to the case or to the wire Avoid the use of MAG2000 to people not educated through the reading of the manual Avoid the use of MAG2000 contemporary with ointments containing free ions of magnetic metals Do not use the device in damp environments and or in presence of inflammable agents
13. e positions on the area to be treated Also in this case take care to place the green side of the therapeutic belt on the skin Tibia fibula I A C E R Srl 16 MNPG52 06 I T EGH MEDICAL DIVISION Femur head Shoulder Vertebral column Lumbar Suggestions for a correct use In P1 P20 programs a longed treatment with an intensity higher than 60 can heat the 3 solenoids belt and this aspect makes therapy less comfortable we recommend to space out treatments and to not go over 2 consecutive hours of therapy In P21 P35 programs we recommend to use the professional solenoids couple available as optional accessories if you want to adjust an intensity higher than 100 and a treatment time longer than 2 hours Do not adjust intensity higher than 50 if you use magnetotherapy carpet optional accessory for prolonged treatments Adjustable programs instructions With MAG2000 you can adjust time therapy and magnetic field intensity parameters as indicated in the following steps I A C E R Srl 17 MNPG52 06 I TECH MEDICAL DIVISION 1 Connect the applicator or the applicators to the device by connecting applicator cable to one of two plugs CH1 CH2 placed on device upper side 2 Connect the power supply cable to the main then connect the power supply plug to the circular connector placed on device upper side near to ON OFF switch 3 Connect the power supply plug to the main 110 230VAC 50 60 Hz 4 Mov
14. e High magnetic field intensity higher than 80 100 Gauss are recommended for short treatments up to 2 hours or in presence of rigid bandages braces WARNING Disconnect the power supply from the main after each treatment We recommend to keep the device in a safe position in order to disconnect easily the cables Place the device on a firm shelf table nigh table away from other devices that could make interferences or stop a safe use of the device and its connected accessories The manufacturer is considered responsible of the performances reliability and safety of the instrument only if e Possible additions changes and or reparations are effected from authorized personnel e The electric plant of the environment in which MAG2000 is inserted it is conforming to the national laws e The instrument is employed in conformity to the instructions contained in this manual Applied parts It s necessary to consider as applied parts not only all accessories belt with 2 3 solenoids professional solenoids couple etc but also the device and the power supply that can get in contact with the user during the treatment Electromagnetic interference Use the MAG 2000 device at least 3 metres away from televisions monitors mobile phones WIFI routers or any other electronic device as they may affect its functioning In particular portable communication equipments as WIFI devices mobile phones cordless phones and their base stations
15. e the ON OFF switch placed on device upper side to the ON position I TECH logo and programs menu will be displayed on screen 5 Select therapy program running through programs menu using A and buttons and put yourself on desired program 6 Press OK Screen will display base setting with therapy time 2 hours and magnetic field intensity 50 int These parameters can be modified as follows I A C E R Srl 18 MNPG52 06 I TECH MEDICAL DIVISION a Press OK button screen displays a moving key icon on the left side b Press A and Vi to adjust the desired therapy hours from 0 to 24 and confirm by pressing OK key Screen will highlight the therapy minutes c Press A and Va to adjust the desired therapy minutes from 0 to 59 and confirm by pressing OK key Screen will highlight treatment intensity I A C E R Srl 19 MNPG52 06 I TECH d Press A and W key to adjust the treatment intensity from 5 to 100 Gauss on P1 P20 programs from 5 to 150 Gauss on P21 P35 programs and confirm by pressing OK key 7 Display will show the step 6 screen highlighting the key icon on the left side press key to highlight the magnet icon 8 Press OK the device will start the treatment displaying on screen the magnet icon with magnetic field flux Green light indicates that therapy is running I A C E R Srl 20 MNPG52 06 9 At the end of therapy the screen will display automatically the menu programs
16. efore cleaning the elastic therapeutic belt with 3 solenoids or the circular cases of professional solenoids couple e Extract the cable with 3 solenoids by removing the 2 silver studs through a screwdriver or open the circular cases through lateral zip e Clean the tissue using water and mild soap and wait for the complete drying before reconnecting the applicators ATTENTION always respect the applicators polarity paying attention to insert the bobbins with the side indicated by symbol turned to the green side of elastic belt therapeutic side Pay attention to respect the temperature humidity and pressure limits mentioned in this manual also during the cleaning of the device and its accessories Carriage and storage Carriage precautions MAG2000 is a portable device so it does not need any particular carriage precautions However we recommend to put away MAG2000 and its accessories in their own bag after every treatment We recommend to not roll up power supply and applicators cables I A C E R Srl 24 MNPG52 06 7 fa O MEDICAL DIVISION Storage precautions MAG 2000 is protected till following environmental conditions Outside of the packaging Temperature from 5 to 40 Rel humidity from 10 to 93 Pressure from 500 to 1060 hPa Inside of the packaging Temperature from 5 to 40 Rel humidity from 10 to 93 Pressure from 500 to 1060 hPa Disposal The equipment is subjected to WEEE regulations see
17. ge selection Move the ON OFF switch placed on device upper side to the ON i position Immediately after keeping pressed the button until the language list appears on the display Release the button select the chosen language by using the A AA buttons Press OK key to confirm your selections Maintenance Functioning control Mag2000 equipment offers a magnet in order to control the device functioning Control procedure 1 switch on the device in according to user manual safety prescriptions 2 starta treatment in according to user manual instructions 3 getthe magnet and put it near to applicator 4 check magnet vibration it will be proportional to selected treatment frequency Please contact the manufacturer in case of magnet vibration absence I A C E R Srl 23 MNPG52 06 _ h 9 MEDICAL DIVISION Cleaning Clean the equipment from the dust using a dry soft cloth Resistant stains can be removed using a sponge soaked in solution of water and alcohol 20 When not using the device for a long time clean the device and its accessories as mentioned before Place the device and the accessories in the carriage bag and store them in their box When using the same applicator belt with 3 solenoids or professional solenoids couple in different patients we recommend to clean it carefully using a sponge soaked in solution of water and alcohol 20 We recommend to disconnect the applicator from the device b
18. ing symbol A Recommended separation distances between portable and mobile communications equipment and the MAG 2000 MAG 2000 is intended for the use in an electromagnetic environment in which radiated RF disturbances are controlled The customer or the user of IMAG 2000 can help prevent electromagnetic interferences by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and MAG 2000 as recommended below according to the maximum output power of the communication equipment Rated maximum Separation distance according to the frequency of the power of the transmitter m transmitter W 150kHz to 80MHz 80MHz to 800MHz 800MHz to d 1 2 P d 1 2 P I A C E R Srl 29 MNPG52 06 h 9 MEDICAL DIVISION For transmitters rated at a maximum output power not listed above the recommended separation distance d in metres 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 2 These guidelines may not apply in all situations Electromagnetic propagation is affected by absorption and reflection from structures objects and people Warranty Make reference to the national laws for any warranty conditions by contacting the national distributor
19. itechmedicaldivision com iacer iacer it You can get any technical documentation on spare parts but only prior business authorization Spare parts For original spare parts contact the National Distributor or the manufacturer at following address ILA C E R S r l Via S Pertini 24 a 30030 Martellago VE ITALY Tel 39 0415401356 Fax 39 0415402684 www itechmedicaldivision com iacer iacer it To preserve product warranty functionality and product safety we recommend to use only original spare parts I A C E R Srl 26 MNPG52 06 EMC tables Electromagnetic emission Compliance Electromagnetic environment guidance Class A Complies RF emissions Cispr 11 RF emissions Cispr 11 Harmonic emissions IEC 61000 3 2 Voltage fluctuations flicker emissions IEC 61000 3 3 MAG 2000 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 MAG 2000 is suitable for use in all establishments including domestic establishments and those directly connected to the public low voltage power supply network that supplies buildings used for domestic purposes The MAG 2000 is suitable for use in all establishments other than domestic establishments and those directly connected to the public low voltage power supply network that supplies buildings used for domestic purposes Electromagnetic immunity MAG
20. known of nor are reported particular contraindications for excessive time length using the device Quick use of the device with presetied parameters We recommend to read the following instructions for an easy and quick use of MAG2000 1 Connect the applicator or the applicators to the device by connecting the applicator cable to one of two plugs CH1 CH2 placed on device upper side 2 Connect the power supply cable to the main then connect the power supply plug to the circular connector placed on device upper side near to ON OFF switch 3 Connect the power supply plug to the main 110 230 VAC 50 60 Hz 4 Move the ON OFF switch placed on device upper side to the ON position I TECH logo and programs menu will be displayed on screen I A C E R Srl 13 MNPG52 06 I TEGR 5 Select the therapy program running through programs menu using and W buttons and put yourself on desired program 6 Press OK Screen will display base setting with therapy time 2 hours and magnetic field intensity 50 int These mean values are recommend by IACER in order to start immediately the treatment 7 Press v button highlighting magnet icon on left down position I A C E R Srl 14 MNPG52 06 SR RA fa ik SLA Wiss SRi mi LO amp U k MEDICAL DIVISION 8 Press OK key The device will start the treatment and on screen will be displayed the magnet icon with magnetic field flux Display green light indic
21. om 21 to 35 maximum magnetic field intensity is 150 Gauss for each channel with solenoids couple applicator Intensity frequency and time values are given with 420 of accuracy The maximum therapy time recommended is 12 consecutive hours Environmental conditions of operation Temperature from 5 to 28 Relative humidity from 10 to 93 Pressure from 500 to 1060 hPa Labelling Label 3 Label 1 back I A C E R Srl 8 MNPG52 06 I TEGG Ball ase lil Ul MEDICAL DIVISION Label details Label 1 MAGNETOTHERAPY MODEL MAG2000 SN 000001 EXT POWER SUPPLY UE24WCP 150120SPA output 15VDC 1 2A GDRE CE IP20 I TECR LACER Stivia S Pertini 24 A 30030 Martellago VE ITALY Label 2 Label 3 Label 4 DC 15V 1 2 A ON OFF CH1 CH2 UE24WCP 150120SPA Symbols description Attention consult operating instructions Product subject to WEEE regulations concerning separate waste collection of electronic equipment a Class Il equipment Applied part type BF Compliance with Directive 93 42 EEC and following modifications Manufacturing date month year I A C E R Srl 9 MNPG52 06 f mi MEDICAL DIVISION Admission temperatures Relative humidity Fabricant information Protection level against solids dusts and liquids entrance device protected against solid foreign objects of 12 5 mm and greater and vertically falling water drops The case of the device guarantees the IP20 level prote
22. or directly the manufacturer IACER a E EY MAG2000 All rights reserved MAG2000 and uenient amisian logos are owned by I A C E R Srl and are registered I A C E R Srl 30 MNPG52 06 I TECH MEDICAL DIVISION I A C E R Srl 31 MNPG52 06 ILA C E R S r l Sede operativa 30030 Martellago VE Via S Pertini 24 A Tel 39 041 5401356 Fax 39 041 5402684 Sede legale S Marco 2757 30124 Venezia Cod Fisc P IVA IT 00185480274 R E A VEN 120250 M VE001767 Cap Soc 110 000 00 i v ww w iacer it iacer iacer it
23. t of the bony pathologies in particular for the osteoporosys Pulsed electromagnetic fields induce biological modifications on biological membrane in order to re establish correct cellular functions According to different authors experiences in osteoporosys a considerable disease regression is evident from the sixth treatment and moreover it s evident an important increase of BMD Bone Mass Density The magnetic field high value Gauss generated by the device allows treatments in presence of braces or plaster bandage I A C E R Srl 4 MNPG52 06 Eire MEDICAL DIVISION Technical Specifications Manufacturer A C E R S r l Via S Pertini 24 a 30030 Martellago VE Tel 39 0415401356 Fax 39 0415402684 www itechmedicaldivision com iacer iacer it IACER S r l is an Italian medical devices manufacturer CE medical certificate n MED24021 issued by Cermet notified b ody n 0476 Declaration of conformity IACER S r l headquartered in Italy via S Pertini 24 A 30030 Martellago VE declares on its own responsibility that MAG2000 is manufactured in conformity with Directive 93 42 EEC MDD dated 14 June 1993 D Lgs 46 97 dated 24 February 1997 Attuazione della Direttiva 93 42 CEE concernente i dispositivi medici Annex Il as modified by Directive 2007 47 CE dated 5 September 2007 D Lgs 37 2010 dated 25 January 2010 Notified body Cermet Via di Cadriano 23 40057 Cadriano di Granarolo BO
Download Pdf Manuals
Related Search