“DETA-Professional”
Contents
1. signature 39 name signature Repairs undertaken by L 201 for warranty repairs to device DETA Professional COUNTERFOIL No 2 Withdrawn cut line Y ELIS Research amp Development Enterprise 124482 Russia Moscow Zelenograd Savelkinskiy Proezd 4 office 2408 Tel Fax 7 495 981 91 60 62 COUNTERFOIL No 2 for warranty repairs to device DETA Professional device Serial No Sale shop name of trading organization Shop seal signature Owner s name and address Signature Works carried out to eliminate the fault Repairs carried out by date signature Owner signature Repair company Company seal 201 Authorized individual signature 40 name signature Repairs undertaken by T 201 for warranty repairs to device DETA Professional COUNTERFOIL No 3 Withdrawn cut line ELIS Research amp Development Enterprise 124482 Russia Moscow Zelenograd Savelkinskiy Proezd 4 office 2408 Tel Fax 7 495 981 91 60 62 COUNTERFOIL No 3 for warranty repairs to device DETA Professional device Serial No Sale shop name of trading organization Shop seal signature Owner s name and address Signature Works carried out to eliminate the fault Repairs carried out by date signature Owner signature Repair company Company seal 2012. 82 h f r h f I 82 82 Adnexitis prostatitis ff h h 82 h f r h f I Chronic appendicitis or 82 x 82 right side adnexitis f f Y h h 82 f Degenerative process h f r h f I in pelvic organs 82 82 68 f f When interpreting the results of topical diagnosis the difference in values of measured levels of individual leads must be taken into account The difference between the measured levels of leads amounting to 6 or more cu s significant evidence of damage in the corresponding quadrant In that case if the difference in measured levels of all leads is less than 6 cu only a judgment about the type of non specific reactivity of the body and tone of the vegetative nervous system can be made 2 Switching the sound on and off in Diagnostics mode The sound is controlled by the q icon on the Therapy panel see fig 7 The position d corresponds to Sound on The MANUAL position corre sponds to Mute 3 Diagnostics with the pharmacological selector On the diagnostics panel press the PROBE button see fig 4 In this case the PROB LED illuminates On the Therapy panel set the THERA PY DIAGNOSTICS key to the DIAGNOSTICS position see fig 4 To work with the pharmacological selector it is necessary to connect the PASSIVE socket see fig 2 with the manual electrode sleeve to connect the selector output SEL see fig 2 to the sec
3. It provides many new opportunities for effective treatment of drug tobacco and alcohol addiction as well as defining side effects of pharmacological agents and their elimination Complex therapy in bioresonance therapy mode with attached autonos ode and drugs from the pharmacological selector provides the possibility of connecting electromagnetic therapy which can cure diseases that were previ ously considered incurable On the Therapy panel set the THERAPY DIAGNOSTICS key to the DIAGNOSTICS position see fig 7 Switch on complex therapy by pressing the COMPLEX THERAPY key Connect the antenna device to the AERIAL socket Switch on BRT mode with the POWER on the BRT panel see item 5 5 In this mode Electromagnetic therapy works but the Electroacupunctural therapy mode does not At the end of therapy switch the device to diagnostics mode by switching off BRT The doctor selects the rules for using this mode using the guidelines for the use of electromagnetic therapy and bioresonance therapy 21 Q Bioresonance therapy mode The appearance of the module for bioresonance therapy is shown in Fig 8 Fig 8 In bioresonance therapy mode the device works with electromagnetic waves of the human body The aim of this therapy is to neutralize the patho logical oscillations in the patient and to activate phylactic power of the body No external energy low
4. by R Voll ATTENTION Extension of the scale is 80 units Not adjustable 17 Electroacupunctural therapy mode The appearance of the module for electroacupunctural and electromag netic therapy is shown in Fig 7 THERAPY e e COMPLE FORM of ou x OR THERAPY DIAGN THERAPY IMPULSE ok on Fig 7 1 Before switching on the therapy it is recommended to set the minimum pulse amplitude by placing INTENSITY to the MIN position 2 Set the polarity of the pulses with FORM IMPULSE and POLARITY buttons 3 Set the desired mode of the device with the AUTO MANUAL key AUTO corresponds to the wave swings in the range 0 1 to 100 Hz MANUAL corresponds to the manual frequency setting in the range 0 1 to 100 Hz 4 AUTO mode With the SPEED knob of CHANGE unit set the required frequency tuning time on the range in wave swings mode For work with children it is recommended to set the minimum tuning time of 1 min For older people set the maximum 3 minutes Switch on the wave swing mode by setting the AUTO MANUAL switch position to AUTO Y Switch on electroacupunctural therapy mode by setting the THERAPY DIAGNOSTICS switch to the THERAPY position The red LED will flash at the rate of pulse repetition In this mode the RANGE knob does not work 5 MANUAL mode
5. frequency ultrasonic etc is used and all variations are physiological This form of therapy is especially effective in cases where the achievement of therapeutic success is impossible with traditional methods or involves a lot of time or expense Above all BRT helps with chronic degenerative diseases rheumatism weakening of the immune system allergies pain of all types neuralgic pains rheumatic neuralgia cancer and postoperative pain indolent wounds asth ma bronchitis gastritis duodenitis ulcers and pain resulting from malignant tumors in the postoperative treatment The therapeutic effect may occur on any organs and organ systems Dis eases where good therapeutic success has been achieved migraine chronic and acute diseases of the lymphatic system heart and cardiovascular disease pancreatitis pancreatic cysts uterine and ovarian cancers diabetes adults and children cystitis nephritis scarring pre operative and post operative treatment allergies sleep disorders and all types of toxic effects including poisoning susceptibility to infections in children 22 Bioresonance therapy is permitted by the Russian Ministry of Health No 2000 47 On the Therapy panel set the THERAPY DIAGNOSTICS key to the DIAGNOSTICS position see fig 7 Switch on BRT mode with the POWER button on the BRT panel see fig 7 or button 1 see fig 6 The doctor selects the rules for usin
6. meridian of the spleen and pancreas consecutively to the BAP of the blad der meridian In the same way measuring of EP BAP takes place with the left hand and left foot Interpreting electrical parameter measurement results of biological active points One of the characteristic features of EAV diagnosis is that it is based on a unified system for assessing EP measurement results of allorgans tissues and the interrelated biological active points Development of this system was preceded by a long period of experimen tal research aimed at finding statistically significant relationships between the values of individual EP BAP in patients with known forms of disease its stages and detectable morphofunctional and pathoanatomical changes in the corresponding organs and tissues 29 CU 100 65 we ewww ewe ce cee wena a wee enw e wane nese seen mene n as eee ees ee sane na see ceesceeesesccsece 50 0 Fig 10 2 4 6 8 t sec The result was the development of a device with a specially graded diag nostic scale on which to evaluate the nature of the damage to various organs and tissue systems The scale is divided into 100 conditional units Among the main diagnostic criteria used to interpret the results of electrical parameters of BAP measurements are three indicators see fig 10 The first of them characterizes the type of reaction related to BAP of or gans and tissue systems in response to irritation by the electric current w
7. of the manufacturer Trans portation of the faulty device is at the buyer s expense Without presentation of a warranty repair coupon and test certificate and or damage to the security seals of the device no claims are admitted and re pair is not performed under warranty The warranty does not apply to the following faults e defects as a result of improper use e defects caused by natural disasters e damage to the security seals e the presence of external defects cracks chips etc The purchaser has the right to have the faulty unit replaced for a new one in the following cases e the device was repaired three times during the warranty period e the device is beyond repair Warranty coupons are enclosed 38 name signature Repairs undertaken by T 201 for warranty repairs to device DETA Professional COUNTERFOIL No 1 Withdrawn cut line ELIS Research amp Development Enterprise 124482 Russia Moscow Zelenograd Savelkinskiy Proezd 4 office 2408 Tel Fax 7 495 981 91 60 62 COUNTERFOIL No 1 for warranty repairs to device DETA Professional device Serial No Sale shop name of trading organization Shop seal signature Owner s name and address Signature Works carried out to eliminate the fault Repairs carried out by date signature Owner signature Repair company Company seal 201 Authorized individual
8. Authorized individual signature 41 name signature Repairs undertaken by L 201 for warranty repairs to device DETA Professional COUNTERFOIL No 4 Withdrawn cut line ELIS Research amp Development Enterprise 124482 Russia Moscow Zelenograd Savelkinskiy Proezd 4 office 2408 Tel Fax 7 495 981 91 60 62 COUNTERFOIL No 4 for warranty repairs to device DETA Professional device Serial No Sale shop name of trading organization Shop seal signature Owner s name and address Signature Works carried out to eliminate the fault Repairs carried out by date signature Owner signature Repair company Company seal 201 Authorized individual signature 42 name signature Repairs undertaken by f 201 for warranty repairs to device DETA Professional COUNTERFOIL No 5 Withdrawn cut line Q ELIS Research amp Development Enterprise 124482 Russia Moscow Zelenograd Savelkinskiy Proezd 4 office 2408 Tel Fax 7 495 981 91 60 62 COUNTERFOIL No 5 for warranty repairs to device DETA Professional device Serial No Sale shop name of trading organization Shop seal signature Owner s name and address Signature Works carried out to eliminate the fault Repairs carried out by date signature Owner signature Repair company C
9. ELIS Research and Development Enterprise peTA Meuis MISSION TO CURE Device composed of electroacupunctural diagnostics pharmacological testing electroacupunctural electromagnetic quantum and bioresonance therapy units DETA Professional Passport Operating Manual and Guidelines woa er a E o a PRO Dna erry o o ee Boog Qe Seo nnou Authors of the operating manual and guidelines S P Konoplev A S Khaynatskiy ELIS Research amp Development Enterprise 2011 All rights reserved Reproduction transmission or distribution of this document or any part of it in any form without the prior written permission of ELIS Research amp Development Enterprise is prohibited Y Contents Description of operation 4 1 Purpose 4 2 Field of application 5 Specifications 6 Package contents 8 Rules for using the device 9 1 Requirements for working conditions 9 2 Device maintenance 9 Description of operating modes 11 Diagnostics mode 13 1 Quadrant leads 14 2 Switching the sound on and off in Diagnostics mode 16 3 Diagnostics with the pharmacological selector 16 4 Diagnostics with ampule drugs 16 5 Diagnostics according to H W Schimmel 17 Electroacupunctural therapy mode 18 Electromagnetic therapy mode 20 Complex therapy mode 21 Bioresonance therapy mode 22 1 Bioresonance cont
10. Electronic pharmacological selector The appearance of the module of the electronic pharmacological selector is shown in Fig 9 Switch on the selector with the E POWER button Connect OUTPUT BRT socket and PASSIVE socket with a short cable Power If necessary turn on the back light in dicator with the LIGHT key On the MEDICAL PREPARATIONS display the message 01 N p_ input N should appear On the numeric key 8 es pad enter the number of the drug using a list of drugs when you enter a wrong number amend it by pressing the lt 4 Gg key Press Now enter the cell number of potency After this the selector will show the name of the drug The drug is Fa we not connected to the chain To connect the drugs to the chain you must press OUT On the selector a message will display Drugs issued N 0 N indicates the number of drugs con nected to the chain Drugs can be discon nected by pressing OUT again To enter a new drug instead of an old e amp a e e O one it is necessary to enter the number EN mo PS 6 of the drug again To enter a new prod Fig 9 uct which will be tested together with the old one it is necessary to press the button and re enter the drugs number The selector permits connection of up to 18 drugs simultaneously Moving through the list of selected drugs with the f and keys Removal of a drug f
11. Electronic pharmacological selector module bioresonance therapy see fig 6 1 Diagnostics module 2 Electronic pharmacological selector module 3 Therapy module 4 Bioresonance therapy module Fig 1 External view of the device Y On the right side of the device are sockets to connect the individual modules together see fig 2 Fig 2 Right side view INPUT BRT bioresonance therapy unit input OUTPUT BRT bioresonance therapy unit output SEL electronic pharmacological selector output AKTIVE active electrode output Connected to the PROBE socket PASSIVE 2 passive electrode outputs PROBE universal diagnostic probe input connection LH left hand output for quadrant leads RH right hand output for quadrant leads LF left foot output for quadrant leads RF right foot output for quadrant leads E me la Fig 3 Rear view On the rear of the unit see fig 3 to the right is the power socket and 12V switch Y in the center is the AERIAL socket for remote antenna connection to carry out electromagnetic therapy the QUANTUM socket to connect the quantum therapy attachment and a socket to connect the BS 7 interface block The device connects to a computer via an external interface block made according to state standard GOST R 50267 0 for medical produc
12. The passive elec trode is connected to the PASSIVE socket and the diagnostic probe is used as active 8 The intensity of the impact by zone is set by the sensations of the pa tient gently rotating INTENSITY knob clockwise until there is a sensation of goose bumps Therapy should not cause pain During therapy on acupunc ture points it is necessary to set the intensity to one third of the intensity of the therapy prescribed for zones Y 9 At the end of therapy switch the device to diagnostics mode by setting the THERAPY DIAGNOSTICS switch to the DIAGNOSTICS position 10 The guidelines for electroacupunctural therapy provide information on the therapy method by zones and by points Electromagnetic therapy mode 1 Set the THERAPY DIAGNOSTICS switch to the THERAPY position The control panel is shown in fig 7 2 To activate electromagnetic therapy the antenna must be connected to the AERIAL socket 3 Set the MANUAL mode of the device with the AUTO MANUAL key this corresponds to the manual adjustment of the frequency range from 0 1 to 100 Hz in electromagnetic therapy AUTO wave swing mode is not rec ommended 4 Set the RANGE and SPEED knobs of the CHANGE unit to the far left position 5 The red LED will flash at the rate of pulse repetition The THERAPY FREQUENCY LCD display shows the exposure frequency The pulse repeti tio
13. The use of syn thetic materials is not permitted 4 Other high frequency or X ray installations must not be located in ad joining rooms 5 The patient must be at least 1 5 m from the television and radio equip ment lighting and electrical appliances Otherwise patients with sensitive brains immediately record higher valuesacupuncture points ATTENTION Static electricity ATTENTION Cover floor with antistatic agent 2 Device maintenance Medical device DETA Professional is designed and manufactured using the latest advances in technology and requires careful handling Follow these guidelines this will help you fulfill the warranty conditions and provide a long fault free service life of the product 1 Keep the device and all its parts and accessories out of reach of children 2 Protect the device and accessories from moisture Precipitation humid ity and all types of liquids contain minerals which cause corrosion of elec tronic circuits 3 Do not use or store the device in dusty or dirty areas This can cause damage to moving parts of the device 4 Do not store the device in hot areas High temperatures can reduce the service life of electronic devices and warp or melt plastic parts Y 5 Do not store the device in cold areas With temperature increasing to normal levels condensation may form inside and damage electronic circuit boards 6 Do not attempt to open the device 7 Protect the device from th
14. ctor it is necessary to connect the PASSIVE socket see fig 2 located on the right side of the device with the with the hand electrode sleeve Connect the selector output SEL see fig 2 to the second socket PASSIVE Insert the diagnostic probe into the socket PROBE Control with the pharmacological electronic selector is described in the chapter Electronic medical selector For diagnosis according to the vegetative resonance test method it is nec essary to select the reproduced point To switch on the vegetative resonance VRT test mode it is necessary to place the probe on the point to be mea sured and then press and hold button 2 on the universal probe see fig 6 for about 1 sec until the VEGATEST see fig 4 LED on the device illumi nates Button 2 does not work while the probe is not placed on the point to be measured indication less than 3 cu Diagnosis is carried out in accordance with traditional method developed by Dr H Schimmel 1 button without function reserve 2 button for VRT mode or switching active points in the EAVPRO program Fig 6 Universal diagnostic probe To turn off the vegetative resonance VRT test mode it is necessary to remove the probe from the point being measured press again and hold ap proximately 1 sec button 2 until the VEGATEST LED turns off The device will transfer to diagnostic mode of the method
15. e jolting and knocks do not drop the device 8 Do not use harsh chemicals solvents for dry cleaning or strong deter gents for cleaning the device 9 Only use the antenna supplied for the device Other antennas may result in damage to the device In the event of malfunction of any part of the device contact the manu facturer The company s employees will assist you and undertake all work re quired Warning The LOW POWER LED signals reduced supply volt gB age In this event correspondence to the device s technical pa rameters with the standards indicated cannot be guaranteed 3 Getting started 1 Connect the AC adapter to the 12V socket on the device The polarity of the voltage does not matter 2 Insert the AC adapter into an wall socket with 220V voltage 3 Turn on the device with the 12V switch On the front of the device the PROB LED should illuminate switch off the machine with the 12V switch and unplug the AC ED Attention After finishing work with patients do not forget to adapter Q Description of operating modes The DETA Professional medical device includes the following mod ules see fig 1 Diagnostics module diagnostics according to R Voll and vegetative res onance test according to H W Schimmel see fig 4 Therapy module electroacupunctural electromagnetic and quantum therapy see fig 4 Bioresonance therapy module bioresonance therapy see fig 5
16. ectro spherical electrodes 3 mm in di ameter with a cross cut EAV experts developed a universal technique of mea suring EP BAP With this EP measurement technique the active electrode probe can be positioned at the center of BAP at any angle since the sphere of the electrode probe provides a reliable contact with it After establishing contact with the BAP the active electrode probe can be rotated in a clock wise direction at the same time increasing the force of pressure on the BAP The transition from search to measurement of BAP electrical parameters is carried out after determining its center by a subsequent change in pressure on it with the active electrode probe before moving to the measurement plateau Moving to the measurement plateau means achieving such pressure with the active electrode probe on the BAP where the increase in pressure on it no longer causes a further rise of the electrodiagnostic device s indicator The optimum pressure of the active electrode probe on the BAP is a value that lies within the following limits for an electrode of 2 mm diameter 500 1 000 gram force for an electrode of 3 mm diameter 600 1 100 gram force for an electrode of 4 mm diameter 700 2 000 gram force Moving to the measurement plateau takes place smoothly over 2 3 sec onds without jerking of the active electrode probe which could result in damage to the epidermis of the s
17. es hyperfunction related to the BAP organ and a slow drop moving to the measurement plateau in 5 sec or more indicates hypofunction It should be noted however that the clinical language terms used to de scribe the results of electroacupunctural diagnostics are generalized and essentially indicate the type of reactions to a pathogenic cause or damage inflammation tumors allergies autoallergy disorders of autoimmunity 33 Y damage to neurohumoral regulation etc which could be designated using other terms used to describe the specific pathological or morphofunctional changes occurring in a particular organ or tissue system For example measurement results of EP BAP vessel degeneration disor ganization of the connective tissue can be interpreted as follows mucoid swelling of connective tissue with superficial disorganization of the interstitial tissue and collagen apparatus TL 100 82 cu ID is absent or is in the interval 100 50 cu on the electrodiagnostic device scale fibrinoid changes with advanced disorganization of connective tissue with formation of various granulomas TL 100 42 cu ID less than 50 cu sclerotic changes in connective tissue with scarring at the location of fi brinoid changes or granulomas calcinomas etc ID below 50 cu Contraindications to use of electroacupunctural therapy Contraindications to the use of ET include benign and malignant tumors hereditary hemo
18. esonance testing according to the method of H Schimmel carry out energy information transfer reprinting of medicinal proper ties of various drugs homeopathic remedies nosodes organ drugs toxins etc on various carriers water alcohol homeopathic grain etc with the possibility of preparing autonosodes conduct electroacupunctural therapy conduct electromagnetic therapy conduct quantum therapy conduct bioresonance therapy according to the method of F Morrell and E Rashe conduct complex therapy mode where bioresonance therapy is con ducted together with electromagnetic therapy with connected autonosode and drugs from the pharmacological selector Y Field of application Field of application for specialists working in specialization 040132 Re generative medicine in accordance with the order of the Ministry of Health of Russia No 241 of 9 June 2003 On the notation of specializations in health care institutions of the Russian Federation centers for homeopathy reflexol ogy and health care institutions etc Designation of device in order medical apparatus for electroacupunctural diagnostics pharmacological testing electroacupunctural and electromag netic therapy DETA Professional model 2011 Y Specifications Diagnostics mode Measurement method n R Voll H B Schimmel Range of variation in conductivity readings CU cee from 0 to 100 Accuracy of measurement in 1 Volta
19. g this mode using the guidelines for the use of bioresonance therapy 1 Bioresonance control The bioresonance therapy module control mode is needed to verify its performance Switch on BRT mode with the POWER button on the BRT panel see fig 8 In this case the corresponding LED illuminates Set VOLUME to 60 units Switch on the Control mode with the Control button In this case the corresponding LED illuminates and an audible signal sounds Switch on the Inversion mode with the INVERSION button The sound will end signaling pathological information suppression mode Switch on the Inversion mode with the INVERSION button again Turn on the LF filter by pressing the LOW button of the FILTERS block Adjustment of the LOW knob verifies the functioning of LFF the sound should fade when the knob is rotated in the direction of 100 Turn off the LF filter Turn on the HF filter by pressing the HIGH button of the FILTERS block Adjustment of the HIGH knob verifies the functioning of HFF the sound should fade when the knob is rotated in the direction of 10 Turn off the HF filter Switch on the Interrupt mode with the INTERRUPT button Set the TIME OF INTERRUPT knob to position 1 There should be a long beep and a short pause At position 15 there should be a short beep and a long pause Switch off Interrupt mode Swi
20. ge on the diagnostic probe relative to hand electrode V l not more than 1 25 Short circuit current UA not more than 12 5 Sound in diagnostic mode sanini tone change Sound control cca cease attrac wc oessdcnen serait Ba Shaken erty Read aad on off LOW power indication n LOW POWER LED Vega test on indication VEGATEST LED Electroacupunctural therapy mode O tp t signal COD incepi positive polarity negative polarity bipolar bipolar inverse Maximum pulse amplitude at load of 100 kOhms V sr 300 Pulse duration at level of 0 5 MS n 1 Range of pulse repetition rate HZ i 0 1 100 Maximum error of frequency setting occ not more than 5 Electromagnetic therapy mode Output signal form bipolar pulse burst with a high frequency Range of pulse packet repetition rate AZ oss 0 1 100 Maximum frequency error of frequency setting not more than 5 Electronic pharmacological selector Number of electronic copies of homeopathic drugs 22 800 Number of free cells to append homeopathic drugs 25 200 Maximum number of drugssimultaneously issued at output 18 Quantum therapy regime Dynamic range HZ onnnnnnnnnnnnnnnunnnnnnnninnnnnnnnnnnnnne Maximum error of frequency setting not more than 5 OptiMUM range NM 468 525 590 660 880 Power AC adapter a 220V 50Hz 12V 0 5A Current consumption not More than A oo cccccccssccesssessessseseee 0 33 Material of hand electrode and ti
21. h consists of successive strengthening and weakening of the pressure force of the active electrode probe to BAP is repeated several times until the position of the electrodiagnostic device indicator is stable If there is no ID effect then the TL value determined during the first sec ond and subsequent measurements does not change If there is an ID effect then the TL value determined during the subse quent measurement of EP BAP is smaller than the first Use of this technical method significantly reduces electroacupunctural diagnosis time and is useful in cases where TL BAP is below 42 cu i e in the interval where the ID registration effect can take quite a long time up to 30 seconds or more The third indicator used in the interpretation of diagnostic results is the asymmetry of TL of paired BAP the difference between which constitutes more than 10 15 cu this is considered as a sign of dysregulation of the func tion of the body or tissue system From the diagnostic point of view registration of this indicator deserves most attention especially in cases where the TL value of all BAP are within 75 50 cu and there is no ID effect Along with this an indirect conclusion that there is dysregulation of or gan functions related to BAP may be obtained by evaluating the speed of the electrodiagnostic device indicator For example a fast abrupt rise of the indicator moving to the measure ment plateau in 1 sec indicat
22. hich shows a particular position of the indicator on the electrodiagnostic device The maximum indicator deviation of the diagnostic device achieved when measuring EP BAP is conditionally denoted in EAV as the testing level TL of BAP For the state of an organ with an extensive inflammatory process purulent process or chronic process during the acute stage of the disease the value of TL for BAP associated with that organ is equal to 100 cu For an acute or catarrhal inflammatory process 99 90 cu For a locally limited inflammatory process 89 82 cu In the initial stages of damage to the function of an organ or tissue system without an inflammatory process the TL BAP is in the 81 66 cu range The condition of physiological tension correspond to the values of TL in the 65 51 cu interval and at an ideal norm is 50 1 cu 30 Y In the initial stages of a dystrophic process the TL BAP value is 49 42 cu and during its progression 41 32 cu In destructive processes with partial atrophy of cellular structures of the organ the TL BAP falls to values in the range of 31 22 cu and in the event of complete atrophy or malignant degeneration 21 0 cu The second indicator of results interpretation of BAP electrical parameters measurement is the effect of indicator drop ID of the device which mani fests itself by the electrodiagnostic device moving in the opposite direction from the established TL value during BAP measureme
23. ical active points To determine the BAP topography the device contains device arrange ment combined with acoustic and indicator display systems When using the acoustic indication system the location of the center of the BAP is determined by the nature of change in tone The location of the center of BAP can be determined by the indicator de viation of the electrodiagnostic device on the indicator display of the diag nostics unit In EAV three techniques are used to find and measure the EP BAP vertical tangent lines 27 Y The vertical technique is used for searching and measuring EP BAP local ized on the feet ear scalp and torso With its use the active electrode probe is set at an angle of 90 to the assumed location of BAP then with weak pressure on the skin moved along the meridian bottom up to define the center point The tangent technique is applied in cases when searching and measur ing EP BAP localized on the fingers With this technique the active electrode probe is set at the center of EAP at an angle of 45 degrees The line technique is used to search for and measure the BAP localized in skin folds such as on the face neck back and buttocks In this case the ac tive electrode probe is moved while held at a slight angle in the area ofthe assumed location of the BAP the center of which is determined by the nature of change in tone Recently with the introduction of el
24. kin in the area ofthe BAP projection The skill of achieving the optimum pressure on the BAP and reaching the measurement plateau is acquired in the process of working with the electro 28 diagnostic device and continuous improvement of measurement techniques for EP BAP In order to optimize and reduce the pressure on the BAP the tip of the ac tive electrode probe can be moistened with 0 9 sodium chloride solution which improves the electrical contact of the probe with BAP and increases the reliability of the electroacupunctural diagnosis For convenience in moistening of the tip of the active electrode probe some experts use a plastic container or a hollow ring containing electrolyte which is worn on the thumb of the free hand of the examiner Sequence of electrical parameter measurement of bio logical active points The sequence of measuring EP BAP of the skin may be different depend ing on the purpose of diagnosis and different authors recommend different point measurement sequences During electropuncture diagnostics in EAV the following sequence of measuring EP BAP of the skin is used Examination begins with the measurement of EP BAP lymphatic system vessel to the BAP of the small intestine meridian with the right hand by plac ing a passive electrode in the left hand After this the passive electrode is placed in the right hand of the patient and measuring of the EP with BAP of the
25. n accompanied by rapid depletion of compensatory abilities of the body and pronounced cell destruction 31 The third indicator of results interpretation of BAP electrical parameters measurement is the dynamics of the arrow s behavior Of great significance for correct diagnosis is the speed of its rise The normal rise time for the arrow is 3 sec If the rise time is less i e 1 2 sec then this is evidence of toxic poi soning in the body This may be the result of taking strong stimulant drugs A slow rise of the arrow indicates fatigue of the body or the patient received took sedatives or sleeping pills on the day of the examination For example a rapid or very rapid effect of ID 1 2 sec expressed by fast movement of the electrodiagnostic device from the original TL towards zero is characteristic of acute intoxication accompanied by rapid depletion of compensatory abilities of the body and pronounced cell destruction At the same time a slow ID observed over 10 seconds or more is most often found in chronic slow moving inflammation processes In addition to these diagnostic criteria quantitative indicators should be taken into consideration in the practice of electroacupunctural diagnosis For example the observation ID for over 20 BAP in different meridians and espe cially on the points of the meridian circulation heart endocrine system of the spleen pancreas liver and kidneys as well as vessels allergies a
26. n rate in normal mode is set with the ROUGHLY and PRECISELY knobs FREQUENCY unit 6 Switch on the electroacupunctural therapy mode by setting the THERAPY DIAGNOSTICS switch to the DIAGNOSTICS position Attention In electromagnetic therapy mode it is not recom mended to change the position of the RANGE and SPEED ce knobs of the CHANGE unit The effectiveness of this therapy is significantly higher than electroacupuncture Withdrawal fre quency effects may occur Attention In electromagnetic mode the INTENSITY knob does not work The impact of the electromagnetic field must be ee strictly measured by dose Electroacupunctural therapy is not switched off in this mode Therefore to avoid accidental elec tric shock it is recommended to set the INTENSITY knob to the MIN position 20 7 The guidelines for electromagnetic therapy provide information on con ducting electroacupunctural therapy ATTENTION Do not leave the unit in THERAPY mode unat tended This could lead to accidental connection of the patient to the electrodes or closing the electrodes circuit Complex therapy mode Complex therapy is a synthesis of bioresonance and electromagnetic ther apy The method is well proven in treating cancer patients This therapy ef fectively removes toxins poisons heavy metals radionuclides drugs and kills germs bacteria and fungi
27. nd button on LH RH panel Foot foot button on LF RF panel Left hand left foot button on LH LF panel Right hand right foot button on RH RF panel Sequence of measuring EP BAZ of skin lead and Relationship with organs and tissue sys polarity of the diagnostic tems current right hand left hand Heart lungs esophagus cervicothoracic area of the spine left hand left foot Heart bronchi lungs stomach descending section of the transverse colon spleen pan 0 creas kidneys urogenital organs Liver gall bladder lungs bronchi stomach ascending section of the transverse colon ap pendix kidneys urogenital organs right hand right foot right foot left foot Urogenital organs rectum in lumbosacral area H of the spine Quadrant measurements are used to carry out preliminary or topical diag nosis the results of which can be further confirmed or refuted by electroacu punctural diagnostics For example in the case of establishing large deviations in TL values from lead norms in right hand foot relating with the liver gall bladder appendix and right ovary special attention in carrying out differential diagnosis should be paid to the measurement of control points of meridians of the liver gall bladder colon bladder etc The following are typical examples of the use of topical quadrant diagnosis Results of measuring EP BAZ Preliminary diagnosis or h h condition
28. nd degenera tion of nerve tissue may indicate the following conditions the prodromal stage of acute infection thrombophlebitis or phlebothrombosis hemorrhagic syndrome acute infectious or chemical intoxication e g food poisoning salmo nellosis alcohol intoxication etc allergic processes pathophysical or pathochemical stage premenstrual tension syndrome or pre menopause conditions espe cially in women with menstruation complications expressed pain syndromes colic in gallstones kidney stones pancre atitis sciatica trigeminal neuralgia etc strong and long term electromagnetic interference in the patient s workplace or place of sleep chronic infectious processes occurring in several organs simultane ously and usually localized in the ENT organs or teeth It should be noted that the ID registration process requires the acquisi tion of certain skills to work with the active electrode probe To simplify the ID registration process it is possible to use a special technique consisting of 32 Y weakening the pressure force with the active electrode probe without its breaking contact from the EAP until the indicator of the electrodiagnostic de vice reaches 0 20 cu After this increasing the pressure force of the active electrode probe for BAP is repeated finishing on the measurement plateau and then the TL BAP is established The method described above whic
29. nt towards zero and a change in the pitch of a sound indicator This indicator is proof of the development of functional or organic chang es resulting from cellular destruction in organs and systems of the organism related to specific BAP In the absence of cellular destruction processes the ID is equal to zero A fall of the arrow by more than 5 cu indicates a pathological condition in the organ For example in acute inflammatory processes with severe cellular destruction the ID may be more than 20 cu with moderate cellular destruction 10 20 cu in damage to the vegetative balance or neurohumoral regulation and also latent inflammatory processes 5 10 cu In analyzing the ID value attention should be paid to the final position of the indicator on the diagnostic tool if the drop ends below 50 cu e g from 80 to 40 cu Such an indicator drop indicates a developing disease process accompanied by irreversible cell damage leading to scarring fatty or other degeneration of the organ An indicator drop not lower than 50 cu indicates retained functions of the organs and tissue systems related to the BAP Some specialists recommend assessing not only the amount but also the speed of the ID indirectly characterizing compensatory abilities and adap tive reactions of the body For example a sharp drop of the diagnostic device indicator 1 2 sec from the original TL towards zero is characteristic of acute intoxicatio
30. ompany seal 201 Authorized individual signature 43 peta Meuis 4 office 2408 Savelkinskiy Pr Zelenograd Moscow Russia 124482 Tel 7 495 981 91 62 7 495 981 91 60 e mail elis deta elis ru www deta elis ru
31. ond socket PASSIVE insert the diagnostic probe into the socket PROBE Control with the pharmacological electronic selector is described in the chapter Electronic medical selector Diagnosis is carried out by the meth od according to R Voll 4 Diagnostics with ampule drugs On the diagnostics panel press the PROBE button see fig 3 In this case the PROB LED illuminates On the Therapy panel set the THERA PY DIAGNOSTICS key to the DIAGNOSTICS position see fig 4 For work it is necessary to connect the PASSIVE socket see fig 2 with the manual electrode sleeve Place the resonator on the stand and connect to 16 the second socket PASSIVE see fig 2 Insert the diagnostic probe into the socket PROBE To conduct a pharmacological test place the ampule in the resonator Instead of ampule drugs cosmetics jewelry and allopathic drugs can be tested If they are being testing it should be taken into consideration that the reaction point occurs later than when testing homeopathic drugs Diagnosis is carried out by the method according to R Voll 5 Diagnostics according to H W Schimmel On the diagnostics panel press the PROBE button see fig 4 In this case the PROB LED illuminates On the Therapy panel set the THERA PY DIAGNOSTICS key to the DIAGNOSTICS position see fig 4 For work with the pharmacological sele
32. p of the universal probe oo csssnentenenteete brass LS59 1 mark State Standard GOST 931 GOST494 PC connection assembly interface BS 7 Average service life years not less than 5 Dimensions without packaging MM oo 240 x 425 x 110 Weight without accessories and spare parts kg oss not more than 2 as a whole unit not More than kg oss not more than 7 Operating conditions ambient temperature from 10 to 35 C relative humidity ca csciircoatsalnaSaarioaascnttencelaauaaannanantiotatesten 80 at 25 C Y Package contents Medical device DETA Professional Hand electrode sleeves Foot electrode plates Universal diagnostic probe Honeycomb cell for ampules Stand dish Electrode for recording on water External quantum therapy attachment Detachable antenna unit BS 7 interface block Power unit Cable set EAVPRO program CD ROM V 4 Documentation set with descriptions and methods Y Rules for using the device Operating conditions 1 Requirements for working conditions 1 Floor coverings in the workplace should not accumulate static charge In bare feet the patient receives the static electricity which leads to incorrect results of diagnostic measurements 2 If the room is covered with carpets of artificial material to eliminate the static charge they must be processed at least twice a week with antistatic agent 3 The chair should be wood and coated with cotton fabric
33. rol 23 2 REPRINTER mode 24 Electronic pharmacological selector 25 Guidelines 27 Requirements for the patient 27 Search technique and electrical parameter measurement of biological active 37 points Sequence of electrical parameter measurement of biological active points 29 Interpreting electrical parameter measurement results of biological active points Contraindications to use of electroacupunctural therapy 34 Safety measures 36 Storage 36 Transportation 36 Certificate of acceptance 37 Manufacturer s warranty 38 Y Description of operation Purpose Medical device DETA Professional TY 9444 001 27970873 2006 hereinafter referred to as the device allows you to measure electrical parameters of biologically active zones BAZ accord ing to the method of R Voll measure electrical parameters of biologically active points BAP using the method according to R Voll including corporal head and auricular points conduct topical syndromic nosological and local assessment of the damage level to the spine sinuses teeth diagnosis conduct pharmacological testing assessment of various pharmacologi cal and non pharmacological drugs for the human body conduct pharmacological testing using the built in DETA Pharma pharmacological selector carry out test measurements of cosmetics jewelry etc for biological compatibility with the human body conduct vegetative r
34. rom the list of those connected takes place by entering a zero 25 Y The medical device DETA Professional electronic pharmacological se lector is supplied as a full version The writing is done for all cells at the selected address starting 4 400 To write information about drugs the drugs must be connected to the INPUT socket of the selector Press WR For 2 3 seconds the display will show Drug write mode The selector will then switch to write drugs mode The display will show the message N write Enter number To continue it is nec essary to enter the write address and press the key If the address is oc cupied the selector will show N write Occupied and find the closest free address If the address is free the selector will write N write Free To write to this address it is necessary to press the WR key The selector will display Save and proceed to the next address In the event of an error the selector will display Write error and proceed to the next address When entering addresses from the Full list of drugs or independently written their names will not appear on the selector display At the same time the issue of drugs will take place on pressing the OUT button Therefore it is important to enter the cell addresses correctly and maintain lists of recorded drugs with care To leave write mode press the OUT key For 2 3 seconds the di
35. rrhagic anemia bleeding disorders purpura and other hemorrhagic conditions pregnancy acute infections and fever conditions of unknown origin chronic infectious diseases in acute stages tuberculosis brucellosis etc decompensated disease of the heart lungs and other internal organs pulmonary fibrosis with a tendency for bleeding active rheumatism myocardial infarction in the last two months venous thrombosis and embolism in the acute period sudden emaciation congenital malformations of the central nervous system the presence of implanted pacemakers in the patient individual intolerance to electric current 34 Q injuries and diseases of the skin in the location of electrical stimulation acute pain syndromes of unknown origin condition of acute psychological stimulation or intoxication The device permits diagnostics and therapy on both corporal acupuncture points as well as auricular acupuncture points 35 Y Safety measures Do not connect the device to an AC adapter with a damaged power cord Do not attempt to repair the device yourself If a fault occurs please con tact a service center Storage The device without packing must be kept indoors at temperatures between 10 to 35 C and a relative humidity of not more than 80 To protect the device from damage it is recommended that the adapter is dis connected from the device when not in use I
36. splay will show the message Leaving write mode The selector may be controlled by a computer using EAVPRO software Version 4 0 for Windows XP Attention When working with a computer the computer must Ee be connected to an isolated power supply unit corresponding to appropriate medical requirements for electrical safety 26 Guidelines Requirements for the patient 1 Three days before seeing the doctor the patient should stop taking drugs herbal infusions except for hormone dependent pa tients and patients receiving hypotension and cardiac drugs discontinue physiotherapy exclude mud therapy and vitamin therapy radiographic and fluoroscopic examinations invasive investigative methods and ultrasound 2 Good personal hygiene should be maintained the day before visiting the doctor do not use cosmetics or perfume ideally do not wear synthetic clothes hands and feet should be clean and nails trimmed 3 When the patient is with the doctor he she removes all clothes and put on a clean white cotton dressing gown not starched he she removes jewelry watches sunglasses hair clips dentures etc he she sits on a wooden stool not varnished or painted and puts his her feet on a wooden rest an ordinary chair covered with a white cotton sheet can be used and instead of a rest thick white cardboard Search technique and electrical parameter measurement of biolog
37. t is recommended that packing materials are retained during the warranty pe riod Transportation Since the device has a high precision liquid crystal indicator which is sen sitive to external mechanical influences during transportation it is recom mended to protect the device from the jolting and knocks not to drop the device not to drop other objects on the device The device must be protected from condensation and the effect of chemi cals 36 Certificate of acceptance DETA Professional device Serial No is produced and accepted in accordance with mandatory requirements of state standards and technical documentation in effect and established as fit for use Technical control mark seal signature name 201 date of issue 37 Y Manufacturer s warranty The manufacturer guarantees that medical device DETA Professional conforms to the specifications during observation of rules of consumer use transportation and storage The warranty period of the device is 12 months from the date of retail sale In the absence of the date of sale and stamp of the trading organization on the coupon for warranty repairs the warranty period is calculated from the date of issue of the device from the manufacturer During the warranty period the owner is entitled to free repairs on presen tation of a warranty repair coupon Warranty repairs are performed on the territory
38. tch off Control mode Turn off BRT 2 REPRINTER mode Substances used for recording the properties of original medicines may include distilled water saline 40 alcohol solution 20 glycerol solution hu 23 Y man blood or plasma lactose wax metals such as aluminum colloid solution and other materials Connect the cup with selected drugs or pharmacological selector to the INPUT BRT socket Connect the cup with the substance for recording to the OUTPUT BRT socket Set the INTERRUPT FILTERS and CONTROL switches to the off position The corresponding LED indicators should not illuminate Switch on INVERSION mode when preparing inverse autonosode Switch on BRT mode with the POWER button on the BRT panel see fig 7 In this case the corresponding LED illuminates Set VOLUME to 30 units To erase information from media it is necessary to connect the cup with the material for recording to the INPUT BRT and OUTPUT BRT and turn on INVERSION At the same cup the selected drugs or pharmacological selector should be switched off The transfer process takes 1 2 minutes depending on the type of medium and its volume Disconnect the cup with the substance for recording from the OUTPUT BRT socket In the case of preparing autonosode it is necessary to follow the guide lines in the DETA BRT user manual 24 Y
39. ts Note In some models the device socket for connecting the BS 7 interface block may be found on the left side of the device Diagnostics mode PROSE LRH LFW ML RH RF Fig 4 DETA Professional medical device allows diagnosis according to meth ods by R Voll and H W Schimmel The diagnostic panel to control diagnosis mode is shown in fig 4 On the device panel between the leads are LEDs indi cating switched on leads in green In electroacupunctural therapy the PROB LED changes to red Red indicates the feed of therapeutic pulses for carrying out electroacupunctural therapy The outputs to connect the electrodes are shown in fig 2 Each of the methods is presented in the classic author version 13 Y 1 Quadrant leads In the diagnostics mode according to R Voll the device allows measure ments by quadrant leads To do this connect LH Left Hand and RH Right Hand sockets located on the right side of the apparatus see fig 2 with the wires to the hand electrodes and the LF Left Foot and RF Right Foot sockets to the foot electrodes Set the switch to Therapy Diagnostics see fig 4 the Therapy panel to the Diagnostics position Give the patient the sleeves of the hand electrodes place the feet on the foot plate electrodes see figure 3 1 The connection diagram is shown in fig 5 Fig 5 The measurements are carried out as follows Hand ha
40. with the possibility of wave swings in a small range Switch on the manual frequency setting mode by setting the AUTO MANUAL switch position to MANUAL Set the THERAPY DIAGNOSTICS switch to the THERAPY position With the frequency change knobs ROUGHLY and PRECISELY of the FREQUENCY unit set the initial tuning rate e g 10 00 Hz Further by turning the RANGE knob of the CHANGE unit from MIN clockwise set the final tuning frequency e g 10 50 H2 After that the device itself will begin to tune the frequency in a linear vari ation in the range 10 00 10 50 Hz and back 10 50 10 00 With the SPEED knob of CHANGE unit set the required frequency tun ing time in this range 6 MANUAL mode without wave swing Switch on the manual frequency setting mode by setting the AUTO MANUAL switch position to MANUAL Set the THERAPY DIAGNOSTICS switch to the THERAPY position Set the RANGE and SPEED knobs of the CHANGE unit to the far left position The pulse repetition rate is set with the ROUGHLY and PRECISELY knobs FREQUENCY unit The red LED will flash at the rate of pulse repeti tion and the liquid crystal THERAPY FREQUENCY display shows the expo sure frequency 7 To conduct electroacupunctural therapy by zone connect the elec trodes to the sockets ACTIVE and PASSIVE see fig 2
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