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MNPG89-01 (Pressoterapia Lymphopress 4 ENG)
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1. 0 to 1060 hPa Inside of the packaging temperature from 10 to 55 C humidity from 10 to 90 pressure from 500 to 1060 hPa IACER SRL Page 19 MNPG89 01 04 05 15 19 MEDICAL DIVISION Disposal The equipment is subjected to WEEE regulations see the symbol VA on the label concerning separate waste collection when disposing this product please use the designed areas for disposing electronic waste or contact the manufacturer Assistance Every intervention on device must be performed by manufacturer For any assistance intervention contact the national distributor or 1 A C E R S r l Via S Pertini 24 a 30030 Martellago VE ITALY Tel 041 5401356 Fax 041 5402684 You can get any technical documentation on spare parts but only prior business authorization Spare parts Contact the distributor or the fabricant for original spare parts at following address 1 A C E R S r l Via S Pertini 24 a 30030 Martellago VE Tel 041 5401356 Fax 041 5402684 To preserve product warranty functionality and product safety we recommend to use only original spare parts Warranty Make reference to the national laws for any warranty conditions by contacting the national distributor or directly the manufacturer IACER IACER SRL Page 20 MNPG89 01 04 05 15 amp MEDICAL DIVISION EMC Tables Guidance and MANUFACTURER S declaration ELECTROMAGNETIC EMISSIONS
2. 21 level protection Not protected against liquids entrance keep dry Relative humidity for product storage Temperature range for product storage Pushing prohibited Sitting prohibited Stepping prohibited amp J IACER SRL Page 10 MNPG89 01 04 05 15 e TECH Working instructions 1 Connect cable to the domestic plug 220 240 VAC then turn ON 1 the ON OFF switch 1 2 Wear the applicators a Leggings use i Wear the leggings or single legging and close the zip up to the end then close the retaining Velcro straps in case of wide circumferences legs connect the extensions available as accessories VELCRO ZIP CONNECTION PLUGS PRESSURE PLANTARS i Insert the pressure plantars under the feet available only with double leggings ii When wearing the leggings pay attention to position the tubes connection cables in the internal side of each legging in single legging version connection cables position is not important iii Connect 4 tubes to the 4 plugs positioned on each legging paying attention to connect the longer tube to the higher position connector darker color of legging thigh IACER SRL Page 11 MNPG89 01 04 05 15 I TECH MEDICAL DIVISION iv After connecting the tubes to the relatives leggings connect the tubes to the air discharge output 5 b Abdominal band use CONNECTION PLUGS i Wear the band and connect the tubes to the
3. FOR ALL THE EQUIPMENT AND THE SYSTEMS LYMPHOPRESSS 4 is intended for use in the electromagnetic environment specified below The customer or the user of the LYMPHOPRESS 4 should assure that it is used in such an environment Emission test Compliance Electromagnetic environment guidance Group 1 LYMPHOPRESS 4 uses RF energy RF emissions only for its internal function Therefore Cispr 11 its RF emissions are very low and are not likely to cause any interference in nearby electronic equipment Class B LYMPHOPRESS 4 is suitable for use in RF emissions all establishments including domestic Cispr 11 establishments and those directly connected to the public low voltage power supply network that supplies buildings used for domestic purposes Harmonic emissions Class A The LYMPHOPRESS 4 is suitable for IEC 61000 3 2 Complies use in all establishments other than domestic establishments and those Voltage fluctuations Complies directly connected to the public low flicker emissions voltage power supply network that IEC 61000 3 3 supplies buildings used for domestic purposes Guidance and MANUFACTURER S declaration ELECTROMAGNETIC IMMUNITY FOR ALL THE EQUIPMENT AND THE SYSTEMS LYMPHOPRESS 4 is intended for use in the electromagnetic environment specified below The customer or the user of LYMPHOPRESS 4 should assure that is used in such environment Immunity test Test 60601 1 2 level EN Comp
4. Lymphatic drainage Lower limbs relief and comfort Substances stagnation prevention in peripheral tissues Blood insufficiency prevention caused by an inadequate pump action Muscle tone loss in disabled or paralyzed patients Compressive limbs therapy substitutes the manual massage for trophic purposes Page 4 MNPG89 01 04 05 15 I TEGE MEDICAL DIVISION Machine body and accessories 3 AIR DISCHARGE OUTPUT PRESSURE ADJUSTEMENT 4 ELECTRIC CABLE 7 EXTENSIONS FOR RO z 0 1 1 DERIVATION CONNECTION TUBES 8 PRESSURE PLANTARS O 1 0 0 9 DERIVATIONS CONNECTION TUBES FOR LEGGINGS JE 13 SPECIAL SPLITTER FOR SIMULTANEOUS THERAPY ON BOTH LEGS AND ABDOMINAL BAND IACER SRL Page 5 MNPG89 01 04 05 15 MEDICAL DIVISION Accessories size Legging e Length around 76 cm from upper side to heel e Thigh circumference around 65 e Ankle circumference around 38 Armband e length around 86 e Biceps circumference around 50 cm e Wrist circumference around 36 cm Abdominal band e Abdominal around 136 cm e Height around 46 cm e Velcro height around 31 cm Extensions e Max width around 13 cm e Min width around 6 cm ACER SRL Page 6 MNPG89 01 04 05 15 amp MEDICAL DIVISION Configurations Lymphopress 4 can be supplied in 5 different versions LYMPHOPRESS 4 TOT compressive limb therapy system comprising machine body double
5. MEDICAL DIVISION User manual MNPGS9 Rev 01 Edition 04 05 15 Pressotherapy model LymphoPress 4 MEDICAL DIVISION I A C E R Srl Via S Pertini 24 A 30030 Martellago VE ITALY Tel 041 5401356 Fax 041 5402684 e mail iacer iacet it http www itechmedicaldivision com amp MEDICAL DIVISION Summary Summary Pressotherapy Machine body and accessories Accessories size Configurations Specifications Technical Specifications Purpose Labels Working instructions Troubleshooting Warnings Cleaning Maintenance carriage and storage Disposal Assistance Spare parts Warranty EMC Tables IACER SRL Page 3 VD o oco N Ui A N N N N NO RP RP RFP rR on PRO o oO DR m MNPG89 01 04 05 15 MEDICAL DIVISION Pressotherapy Compressive limbs therapy is able to promote a right venous circulation by decreasing muscle tension caused by stress or chronic and acute pains thanks to its pump action it favorites venous return by increasing tissues blood circulation and finally their physiological renewal Compressive limbs therapy can solve blood stagnation problem in damaged sanguine vessels or in body zones not correctly bedewed External compression allows excess interstitial fluids to return in circulatory system in order to be quickly removed Most co IACER SRL mmon applications are Body massage increase Blood flow promotion thanks to a slow and progressive pressure
6. band plugs paying attention to connect the longer tube to the higher position connector on abdominal band ii After connecting the tubes to the band connect the tubes to the air discharge output 5 b Simultaneous use of double leggings and abdominal band i Connect the special splitter for simultaneous therapy 13 to the air discharge output 5 Then connect double leggings and abdominal band connectors to the splitter IACER SRL Page 12 MNPG89 01 04 05 15 I TEGU MEDIGAL DIVISION ii Wear the leggings or single legging and close the zip up to the end then close the retaining Velcro straps in case of wide circumferences legs connect the extensions available as accessories iii Insert the pressure plantars under the feet available only with double leggings iii When wearing the leggings pay attention to position the tubes connection cables in the internal side of each legging in single legging version connection cables position is not important iv Connect 4 tubes to the 4 plugs positioned on each legging paying attention to connect the longer tube to the higher position connector darker color of legging thigh iv After connecting the tubes to the relatives leggings connect the tube to the splitter connected 1o the air discharge output 13 v Wear the band and connect the tubes to the band plugs paying attention to connect the longer tube to the higher position connector on abdomina
7. e Check if there are any damages and or holes in the tubes and connectors e Check the applicators right connection to leakage the main body e Check if the tubes are pressed or bent There is no e Check the applicator right connection to pressure or the air doesn t go into the applicators the main body e Check if the tubes are pressed or bent e Check if the compression chambers swell up in a progressive way Air goes into the compression chambers and or an air leakage is present in the applicators e Check if there any holes or damages in the compression chambers If there are not any air leakages switch off the device then switch on it and re check the right working ATTENTION with Lymphopress 4 double leggings version always connect both leggings to the connection tube even if you use only one legging during the treatment IACER SRL Page 15 MNPG89 01 04 05 15 MEDICAL DIVISION Warnings The following warnings guarantee user safety and prevention against damages and or lesions Please read it carefully before using LymphoPress 4 Warning In case of not following the instructions the user may suffer from serious injuries Indications O Prohibition indication This is an indication for D not disassembling Caution In case of not following the instructions the user may suffer from injuries or device damages Pay attention Disconnect the cable from domestic
8. ertificate e Equipment not protected against liquids penetration e Equipment and accessories not subjected to sterilization e Use of the equipment is prohibited close to flammable substances or in environments with high concentrations of oxygen e Continuous operating mode equipment e Equipment not suited to be used in external Technical Specifications Power Supply 220 240 VAC Therapy time Impostabile 030 50 60 Hz min Current 0 2 A Max pressure 300 mm Hg 10 Max output 25 W Weight 2 Kg power Purpose Clinical Purpose Therapeutic Use Clinic and domestic use ACER SRL Page 8 MNPG89 01 04 05 15 O MEDICAL DIVISION Labels Compressible Limb Therapy System 0476 Model LYMPHOPRESS 4 Voltage AC220 240V Frequency 50 60Hz ud a name 50VA pre 300mmHg 10 SN AADAMA rm o Fo mx 1 A C E R srl Via Sandro Pertini 24 A I TE 4 30030 Martellago VE Italy MEDICAL DIVISION Warning gt PP Product subject to WEEE regulations concerning separate waste collection of electronic equipment Applied part type BF Class Il equipment DPI oN rN ic X D Compliance with Directive 93 42 EEC 5 Manufacturing date IACER SRL Page 9 MNPG89 01 04 05 15 E O MEDICAL DIVISION Attention consult operating instructions Instructions for use HO 5 IP Device with IP
9. 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 a following symbol A Recommended separation distances between portable and mobile communications equipment and the EQUIPMENT LYMPHOPRESS 4 is intended for the use in an electromagnetic environment in which radiated RF disturbances are controlled The customer or the user of LYMPHOPRESS 4 can help prevent electromagnetic interferences by maintaining a minimum distance between portable and mobile RF communications equipment transmitters and LYMPHOPRESS 4 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 AP d 1 2 AP 2GHz d 2 3 AP 0 01 0 12 0 12 0 23 0 1 0 38 0 38 0 73 1 1 2 1 2 2 3 IACER SRL Page 23 MNPG89 01 04 05 15 E O MEDICAL DIVISION 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 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 acc
10. l band vi After connecting the tubes to the band connect the tubes to the splitter connected to the air discharge output 13 c Armband use i Wear the armband and connect the tubes to the armband plugs paying attention to connect the longer tube to the higher position connector darker color on armband ii After connecting the tubes to the armband connect the tubes to the air discharge output 5 IACER SRL Page 13 MNPG89 01 04 05 15 ITECH 3 Therapy time selector 2 on machine body a Therapy time can be adjusted from 0 to 30 minutes pump motor of main body will start operating b The air will fill up in applicator chambers in 2 minutes Attention The time selector cannot be moved counterclockwise during the treatment Please wait the session end to adjust a new therapy time 4 Pressure regulator selector 3 on machine body Air pressure in compression chambers be adjusted from 0 to maximum pressure around 300 mmHg 20 by rotating the knob in clockwise a Start the treatment with a middle pressure and increase it progressively according to your needs IACER SRL Page 14 MNPG89 01 04 05 15 ll amp MEDICAL DIVISION Troubleshooting Problem Solution LymphoPress 4 e Check the connection to the domestic doesn t switch on plug e Check the ON OFF button e Check the power supply status no sign of damages LymphoPress 4 emits a strange sound like air
11. legging 6 2 derivations connection tubes 9 2 pressure plantars 8 armband 11 abdominal band 12 1 derivation connection tubes 10 special connector for simultaneous therapy on both legs and abdominal band 13 LYMPHOPRESS 4 LEG2 ABD compressive limb therapy system comprising machine body double legging 6 2 derivations connection tubes 9 2 pressure plantars 8 abdominal band 12 1 derivation connection tubes 10 special connector for simultaneous therapy on both legs and abdominal band 13 LYMPHOPRESS 4 LEG2 compressive limb therapy system comprising machine body double legging 6 2 derivations connection tubes 9 2 pressure plantars 8 LYMPHOPRESS 4 LEG1 compressive limb therapy system comprising machine body single legging 6 1 derivation connection tubes 10 LYMPHOPRESS 4 ARM1 compressive limb therapy system comprising machine body armband 11 1 derivation connection tubes 10 Extensions for wide legs 7 and special connector for simultaneous therapy on both legs and abdominal band 13 are available as accessories Single accessories are available as optional to complete Lymphopress 4 content and potentiality IACER SRL Page 7 MNPG89 01 04 05 15 LO MEDICAL DIVISION Specifications Lymphopress 4 has the following specifications e Class lla equipment Directive 93 42 EEC annexed IX rule 9 e Class ll applied part type BF Classif CEI EN 60601 1 e CE0476 c
12. liance level Electromagnetic environment guidance Electrostatic discharge ESD EN 61000 4 2 6kV contact 8kV air t 6kV contact 8kV air Floors should be wood concrete or ceramic tile If floor are covered with synthetic material the relative humidity should be at least 30 IACER SRL Page 21 MNPG89 01 04 05 15 E e MEDICAL DIVISION Electrical fast 2kV for power t 2kV per power Mains power quality transient burst supply lines supply lines should be at that of IEC 61000 4 4 a typical commercial or hospital environment Impulses 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 LYMPHOPRESS 4 requires continued 70 Ur 70 Ur operation 30 dips of Ur 30 dips of Ur during power mains per 25 cycles lt 5 Ur gt 95 dips of Ur per 5 seconds per 25 cycles lt 5 Ur gt 95 dips of Ur per 5 seconds interruptions it is recommended that LYMPHOPRESS 4 be powered from an
13. me or on its parts connector tubes applicators if you use the device in cold places a etc malfunctioning may happen make it operating by changing progressively the intensity for 3 4 times Clean the device using a dry soft cloth Do Do not bend or tie the connection tubes not use cleaning solvents or other chemical substances in order to avoid any damages Use the device only for expected Product subject to WEEE regulations purposes concerning separate waste collection of electronic equipment IACER SRL Page 18 MNPG89 01 04 05 15 l 8 19 MEDICAL DIVISION Cleaning Clean the device and its accessories using a soft cloth Resistant stains can be removed using a sponge soaked in solution of water and mild soap Wait for the complete drying before using the device and its accessories Do not use chemical substances solvents or cleaners to avoid device and accessories damage Maintenance carriage and storage If it is used in accordance with the instructions of the user manual the device does not need a particular regular maintenance Carriage precautions It doesn t need any particular carriage precautions however we recommend to put away Lymphopress 4 and its accessories in their own box after every treatment Storage precautions Lymphopress 4 is protected till following environmental conditions Outside of the packaging temperature from 5 to 40 C humidity from 30 to 80 pressure from 50
14. ording 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 LymphoPress 4 All rights reserved LymphoPress 4 and memen afar logos are owned by 1 A C E R Srl and are registered IACER SRL Page 24 MNPG89 01 04 05 15 1 A 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 MA 00185480274 REA VEN 120250 M VE001767 Cap Soc 110 000 00 www iacer it iacer iacer it
15. plug N Danger Do not use the device in presence of acute inflammations or injuries Infections risk IACER SRL Page 16 Please consult the doctor in case of cancer intestinal problems fractures acute thrombosis and other invalidating pathologies MNPG89 01 04 05 15 I TECH MEDICAL DIVISION Do not use the device if you feel pain or Do not exceed 20 minutes in the first i treatments We suggest to start with bad feelings treatments of 5 10 minutes Attention do not spill liquids or any substances on the device Liquid penetration could damage the device In case of suspected malfunctioning do Do not connect or disconnect the device not open or repair the device Do not use from domestic plug with wet hands the device Electric shock risk Contact Electric shock risk the distributor or fabricant Use the device only with 220V power Do not press bend or damage the supply Electric shock risk Disconnect electric cable Electric shock risk the device from domestic plug when not in use Avoid to connect more devices to the Avoid device hits or drops same multiple plug Overheating risk IACER SRL Page 17 MNPG89 01 04 05 15 I TECU MEDICAL DIVISION N Cautions Do not move when the device is working Do not expose the device to the sun and do not storage it next to heat sources Do not place any objects on the device or If you not use the device for a long ti
16. uninterruptible power supply or a battery Mains power 3 A m 3 A m Mains power quality electromagnetic field should be at that of EN 61000 4 8 a typical commercial or hospital environment IACER SRL Page 22 MNPG89 01 04 05 15 MEDICAL DIVISION Guidance and MANUFACTURER S declaration ELECTROMAGNETIC IMMUNITY FOR ALL THE EQUIPMENT AND THE SYSTEMS THAT ARE NOT LIFE SUPPORTING LYMPHOPRESS 4 is intended for use in the electromagnetic environment specified below The customer or the user of LYMPHOPRESS 4 should assure that is used in such environment Immunity test Test level EN Compliance Electromagnetic 60601 1 2 level environment guidance Conducted RF 3 Veff from 3 Veff from Portable and mobile RF EN 61000 4 6 150kHz to 80MHz 150kHz to 80MHz communications equipment RF Radiata 3 Veff from 3 Veff from should be used no closer to EN 61000 4 3 80MHz to 2 5GHz 80MHz to 2 5GHz any part of LYMPHOPRESS 4 including cables than the recommended separation distance calculated from the equation applicable to the frequency of the transmitter Recommended separation distance d 1 2 150kHz to 80MHz d 1 2 80 MHz to 800 MHz 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
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