User manual User manual
Contents
1. Uy Type B applied part Observe accompanying documents The product and its packaging may not be disposed of as household waste but has to be sent back to the manufacturer for disposal Al O www vadoplex com N Safety notes Do not use the VADOplex system without having received a technical instruction on its use Before switching the device on to using it for therapy make sure to read and understand the manual and test the application of the device Always be aware of the limits and risks when using the device Make sure to observe all preventive safety and operation instructions attached to the device Pay special attention when using the device on or in the presence of children Do not use the VADOplex system for purposes other than those described in this manual Never pull at the cable to disconnect the device from the power supply but always take the cable at its plug Make sure to have the device switched off before leaving it unsupervised When carrying transporting and storing the VADOplex system take care not to damage the system by dropping it or by trans porting or storing it incorrectly Make sure that the device is properly electrically grounded by ensuring that it is only connected to a grounded power supply fulfilling the applicable national and local electrical regulations Do not use the VADOplex system outside or on wet surfaces Do not use the VADOplex system in the vic2. in the area of the ankle and wrist After compartment syndrome Shoulder injuries and surgery For quick drainage of chronic edema of the legs and arms e g chronic lymphedema chronic venous insufficiency POPP OOO EEE EEE EEE EEE EEE EEEEEER For compartment prophylaxis in case of serious soft tissue damage CEEE EEE EEE EEE EEE Prevention of deep vein thom bosis when used solely e g in case of HIT or heparin intolerance Prevention of deep vein throm bosis as additional measure to anticoagulant drugs or for low risk patients CEEE EEE EEE EEE EEE EEE EEE EEE Chronic recurrent ulcera cruris arterial venous mixed Venous congestion COCO COLE EEE EEEOOET ESE ESEHESOSEEOEEESEEHOEOESESEOSEEEE EDEL Peripheral artery occlusive disease PAOD and arterial circulatory disorders of the extremities Recommended application time EESC EEE EEE post traumatic continuous with breaks if required postoperative 6 to 8 hours daily with breaks if required At least 4 hours per day with breaks if required over several weeks EEE EEE EEE EEE EEE EEE EEE EESC EEE EEE cn ccrrnrrnccon ce cor At least 11 hours per day gradu ally reducing the application time until full load is possible At least 6 hours per day in the high risk phase gradually reducing the application time until full load is possible At least 4 hours per day with breaks if required over several weeks At least 4 hours per d
3. Useful details Useful details Technical data Device dimensions MDD class la 93 42 EEC Annex IX Rule 9 Height 23 cm overall Protection class Type B Depth without handle 15 5 cm CE certification No CE 0123 Width 35 cm 0123 Weight 4 3 kg Rating Warranty and guarantee Input 230 V 50 Hz 0 4A For the VADOplex system a guarantee period of year after delivery to the hospital or distributor is granted Power supply Manufactured by Mean Well Enterprises Co Ltd Power supply model PD 25B Fuses 2xT1A250V DIMDI No 10 969 in accordance with UMDNS Classification UMDNS compression device intermittent Code of the authority responsible DE CA 57 Upper Bavaria This device is intended for continuous use EMC tested in accordance with IEC 60601 1 2 For information about potential electromagnetic interference and advice on how to avoid or minimize such interference please refer to the attachment of this user manual Environmental conditions for transport storage Temperature range 20 Cto 60 C Relative humidity up to 95 without condensation Ambient pressure 700 hPa to 1 060 hPa Environmental conditions during operation Temperature range 10 Cto 40 C Relative humidity up to 95 without condensation Ambient pressure 700 hPa to 1 060 hPa Before opening the device unplug the power supply a gt The device meets all essential requirements of the applicable EU guidelines o N
4. VADOG User manual OPED to make you stay mobile OPED is specialized in medical techno logy that gets patients back on their feet more quickly after injury We care for patients with a whole range of orthopedic rehabilitation products All orthoses are developed and manufac tured in Germany With a great spirit of innovation OPED is working to ensure that doctors can offer their patients optimum care with highly functional treatment concepts OPED GmbH Medizinpark 1 83626 Valley Oberlaindern Germany Fon 49 0 8024 6081 82 10 Fax 49 0 8024 6081 82 99 mail oped de www oped de OPED AG Hinterbergstrasse 26 6330 Cham Switzerland Fon 41 0 41 748 53 35 Fax 41 0 41 748 53 40 contact oped ch www oped ch OPED UK Ltd Unit 2 Glenmore Business Centre Waller Road Hopton Industrial Estate Devizes SN10 2EQ United Kingdom Phone 44 0 1380 722177 Fax 44 0 1380 721960 enquiries oped biz www oped de OPED Australia Pty Ltd 4 42 Greenacre Rd Wollongong NSW 2500 Australia Phone 61 0 2 4226 5880 Fax 61 0 2 4226 5881 contact oped australia com au www oped com au OPED USA 203 Crescent Street Suite 205 Waltham MA 02453 USA Phone 1 877 673 3426 Fax 1508 879 0769 hello opedinc com www opedinc com www vadoplex com Table of contents Device description Front side Connecting tubes to garments pads Display eorrcorcrrrnroccrcnrrnnccrrrnnnsssssso Control panel Toggle swit
5. ay with breaks if required over several weeks POPC OSE COLOCO LECCE OLL OCO ossos ODORS At least 4 hours per day with breaks if required over several weeks www vadoplex com Contraindications For the following types of patients risks and benefits have to be assessed Patients whose heart could be impaired by an increased reverse current patients with decompensated cardiac insufficiency acute deep leg vein thrombosis or pulmonary embolism as well as throm bophlebitis or massive infections of the extremities treated If you have any question please ask your doctor Alarms trouble shooting Error code 1 Air tube disconnected exchange pad Error code 2 Air tube bent Error code 3 Pressure too low exchange pad Error code 4 Pressure too high exchange pad www vadoplex com Application note Do not expose the VADOplex device to extreme temperatures water or humidity Do not drop the device and do not use force trying to open it Should one of these events happen have the device inspected by an authorized service technician Opening the housing or exposing the device to humidity dampness creates a risk of electric shock Using the device near inflammable gases can cause explosive inci dents Do not place the device in the vicinity of such gases The device may only be used with the pads intended The pads have to be disposed of properly by medical staff Cleaning maintenance and tech
6. ch on off EEE EEE EEE EEE EEE EEE EEE EEE EEE EEE EEE EEE EEE EEE EEE EEE EEE Rear side Two tube connections to the garments pads Transport handle and bed mounting Ventilation slots Information on error messages 1 4 Supply cable connection Control panel Control panel buttons Start Stop Individual pressure Mode button button adjustment 30 80 J l secs Start Stop Pressure setting reached OK displayed as soon Left side as set pressure is Pressure setting Right side Application time in seconds left side Getting started Application time in seconds right side Display between pressure pulses a Display during pressure pulse 1 Plug the two connecting tubes into the corresponding sockets at the rear side of the device one on the left and one on the right 2 Plug the supply cable into a power socket 3 Attach the VADOplex garments pads and make sure that they are positioned properly see user manual supplied with pressure sleeves The pads are to be used for one patient only and may neither be used for several patients nor refurbished www vadoplex com Control panel 4 Connect the transparent tubes of the VADOplex pads to the connecting tubes of the VADOplex device 5 Switch on the device with the toggle switch at the front and wait until the following is displayed 6 Press the start stop button to sta
7. inity of flammable anesthetic mixtures with air oxygen or nitrous oxide Make sure that the device is positioned on a solid and flat surface providing the necessary stability when in use Parts of the device could burn or catch fire if exposed to an ignition source Do not smoke during use of the VADOplex system and do not expose it to open fires The VADOplex system is designed in a way protecting it from being affected by incontinence Nonetheless preventive measures to avoid the device from coming into contact with fluids should be taken Always make sure to unplug the supply cable before maintenance and cleaning tasks are performed Not unplugging it could cause electric shock or injuries Only use the device if it is dry and only if your hands are dry to avoid the risk of electric shock due to humidity Do not use the VADOplex system as a toy The openings on the device rear side are for ventilation purposed and protect the device from overheating It is thus not permitted to cover these openings www vadoplex com
8. nical service Only employees who have undergone the corresponding technical training from the manufacture are authorized to open the device and perform maintenance tasks The VADOplex system has to be maintained every 3000 operating hours or at least once a year During maintenance the hardware and software of the device is inspected wear parts are checked and if applicable exchanged or cleaned This inspection requires special training to ensure smooth operation of the VADOplex systems Thus maintenance tasks and technical procedures at the VADOplex system may only be performed by authorized technicians Otherwise the manufacturer does not assume any responsibility for the use and effect of the VADOplex system The case of the device and the connection hoses can be wipe dis infected with standard disinfectant agents for hospital use or alter natively with a 1 sodium hypochlorite solution Residues of alcohol and sodium hypochlorite remaining on the surfaces after wipe disinfection must be removed with a water moistured cloth The user patient does not have to clean the device This is done by the service staff during maintenance repair The VADOplex system does not have to be sterilized You can simply wipe the housing and connection tubes with common disinfectants On request the manufacturer can supply circuit diagrams spare parts lists and other documents for use by qualified expert staff www vadoplex com
9. rt the therapy By pressing the start stop button during therapy you can interrupt the procedure for a break Pressing the button again reactivates the device AAA Set mode via Individual pressure regulation S With the button you can choose from 3 basic modes Standard mode 130 mmHg for 1 second for application at the foot 130 mmHg for 3 seconds for application at the foot in case of arterial circulatory disorders 80 mmHg for 1 second for application at the hand The factory set standard mode is 130 mmHg for 1 second Always chose the modes by pressing the a button only If you want to delete your settings simply switch off the device with the toggle switch and then switch it back on Note If 3 seconds application time is set up for both sides the interval between the impulses will raise automatically from 20 seconds to 50 seconds due to slower venous refill time with arterial diseases Indications Intended use Device for improvement of the venous return and arterial flow with intermittent pneumatic impulse compression on the upper and lower extremity It is equally suitable for specialist staff in hospitals as well as for application at home with the patient or his relatives using the system themselves Indication EEE EEE EEE EEE EEE EEE For quick drainage of acute edema of the upper and lower extremities e g post traumatic and postoperative Especially suitable for fractures
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