Deta-Elis DETA AP-13 User manual

MISSION TO CURE
Electromagnetic Field
Treatment Device
DETA AP-13
Passport
The latest scientic opinions on the ght against parasites
A unique medical procedure
ELIS Research and Development Enterprise

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© ELIS Research & Development Enterprise
All rights reserved. Partial or complete photomechanical reproduc-
tion and recording onto electronic media is prohibited.
Printed in Moscow.

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1. Introduction 2
2. Purpose 3
3. Main specications of the device 4
4. Package contents 4
5. Information about the device 5
6. Getting started 6
7. Operation 7
8. Directions for use of the device 8
9. Contraindications to use 9
10. Storage 9
11. Transportation 9
12. Manufacturer’s warranty 9
Contents

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1. Introduction
Treatment device “DETA-AP-13” ТУ 9444-001-27970873-2006
(hereinafter referred to as the device) is designed for electro-
magnetic therapy.
The device is designed for individual use:
• In clinical practice by doctors of various specializations.
• Outpatient use.
Certicate of conformity РОСС RU.ИМ24.В03109
Registration certicate No. ФСР 2009/05641
Designation of device in order: device “DETA-AP-13”

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2. Purpose
Treatment device “DETA-AP-13” is designed for exogenous
bioresonance therapy of a wide range of diseases via the eects
of electromagnetic low-energy radiation on the body.
The device operates at frequencies that allow you to conduct
therapy for infectious diseases and those associated with in-
fection with programs especially designed for the device. The
method of using the programs is simple, easy to understand,
and requires no special training. The strong therapeutic eect is
achieved due to the deep penetrative capability of the electro-
magnetic eld on the body. The high precision rate of setting
the frequency provides the possibility of aiming at a particular
type of infectious pathogen and destroying it.
The therapeutic eect when using “DETA-AP-13” is based on
the latest scientic opinions set out in guidelines.
The “DETA-AP-13” portable device, programmable with a
computer allows you to conduct therapy using any of 13 pro-
grams. Each program is designed to treat a particular disease or
group of diseases.

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3. Main specications of the device
3.1. Number of programs 13
3.2. Frequency range 0.1 Hz ÷ 10 kHz
3.3. Continuous operating time of the device:
not less than 10 hours
3.4. Power supply:
2 AA batteries, 1.5 V
2 Ni-Mn AA batteries, 1.2 V
AC adapter 220 V/50 Hz – 7.5÷12 V/0.1 А
(supplied optionally)
3.5. Total dimensions of the device:
not more than 105 х 65 х 20 mm
3.6. Device weight: not more than 0.15 kg
3.7. Average service life of the device minimum 5 years
Attention! When using batteries, a continuous operating time
depends on a battery capacity.
4. Package contents
• Medical device DETA-AP-13 1 pc.
• Passport 1 pc.
• Guidelines 1 pc.

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Fig. 1 - Front panel:
• Power button
• Arrows and to alternate between programs
• Button to start and stop programs
• Screen (switched on).
Fig. 2 - Side panel.
The side panel of the device has two sockets:
a) a round socket for an AC adapter.
b) a rectangular socket for device programming. Program-
ming the device is performed using programs “Therapy 7”
(or higher versions) and programmer. The program and pro-
grammer are supplied optionally. The device can be repro-
grammed any number of times.
Fig.1 Fig. 2
5. Information about the device
b
а

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6. Getting started
6.1. Insert the batteries into the battery compartment, observ-
ing correct polarity. The device will now start and perform a
test for functionality. The appearance of a message on the dis-
play and audible signal indicates the functionality of the de-
vice.
6.2. When using an AC voltage source, connect an AC adapter
to the device before connecting it to the wall socket.
6.3. To change the batteries, open the battery compartment on
the bottom of the housing (see Fig. 3) carefully pushing back
the cover latch
The device retains the stored treatment programs when chang-
ing the batteries.
Attention! The device has an add-in unit warning of the battery dis-
charge with an audio signal of three beeps. In which case, the display
shows “LOW BATTERY”, and the device switches o. To continue opera-
tion, it is necessary to change the batteries or connect an AC adapter.
Fig.3

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7. Operation
7.1. Switch on the device, by pressing and holding it for 3
seconds (protection against accidental operation). A single au-
dible signal should sound. The display will read: the name of
the program in the top row, and the bottom line will contain
the program time in hours:minutes:seconds, and the battery
indicator.
7. 2. After switching on, the device switches to «Select Program».
If no programs have been selected within 30 seconds, the de-
vice switches o. Programs are selected by clicking on the ar-
rows or to navigate through the list of programs.
7. 3. To start the program, press . The device will count down
in reverse order. The countdown to zero will switch o.
7.4. You can stop the program by pressing button . The pro-
gram stops and the device switches to “Select Program”.
Pressing again restarts the program.
7. 5. To switch the instrument o, press button and hold for
3 seconds until the audible signal.
7.6. For the device to take eect, place the device with the keys
facing away from you at a distance of not more than 0.5 m, e.g.
in your breast pocket.

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8. Directions for use of the device
Point of eect. Due to the high penetrative capability of the
electromagnetic eld, it is not necessary to remove clothing. It
is necessary to place the device close to the pathological focus
to obtain the most pronounced therapeutic eect.
Using the device. Session - this is a one-time therapeutic
eect, during which there is destruction of a certain type of
pathogen or elimination of pathological changes in tissues
within a set framework of frequencies. The most pronounced
therapeutic eect results from a course of treatment.
Course of treatment - this is several sessions. The course
duration is determined by the resistance of the pathogen to
exposure of the resonance frequencies, and also the degree
of pathological changes to organs and tissues (see guidelines).
Before conducting therapy, a diagnosis must be established
and the infectious pathogen identied for correct program
selection. Diagnostics must be used for this. When the patho-
gen has been identied, programs are selected aimed at the
eliminating it. After treatment, it is recommended to tests are
undergone to ensure the problem is resolved. If the problem is
not completely resolved, treatment must be repeated.
It should be noted that during therapy, the underlying dis-
ease may be aggravated, which may be accompanied by gener-
al tiredness, a temperature, weakness, etc., which is associated
with the elimination of the infectious pathogen. In this event,
you should use detoxication programs more frequently, and
drink sucient pure drinking water. The treatment course pro-
cedure indicated for each disease should be strictly adhered to
in order to attain maximum benets.

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9. Contraindications to use
Contraindications to independent use include:
• urgent conditions requiring immediate medical interven-
tion;
• signs of severe illness with organ failure (cardiovascular, liver,
kidney, failure etc.).
In this case, therapy is only carried out under medical supervi-
sion.
10. Storage
The device without packing must be kept indoors at tem-
peratures between 10 to 35 °C and a relative humidity of not
more than 80%.
It is recommended that packing materials are retained dur-
ing the warranty period.
11. Transportation
Since the device has a liquid crystal display screen which is
sensitive to external mechanical inuences, during transporta-
tion it is recommended:
• 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 ef-
fect of chemicals. For long-term storage of the device, remove
the batteries from the battery compartment.
12. Manufacturer’s warranty
The manufacturer guarantees that medical treatment device
“DETA-AP-13” conforms to the specications during observa-
tion of rules of consumer use, transportation and storage.
The warranty period of the device is 18 months from the date
of retail sale.

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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 re-
pairs on presentation of a warranty repair coupon. Warranty
repairs are performed on the territory of the manufacturer.
Transportation of the faulty device is at the buyer’s expense.
Without presentation of a warranty repair coupon and test
certicate and/or damage to the security seals of the device,
no claims are admitted and repair is not performed under war-
ranty. Warranty coupons are enclosed.
The warranty does not apply to the following faults:
• defects as a result of improper use;
• defects caused by natural disasters;
• damage to the security seals;
• 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:
• the device was repaired three times during the warranty pe-
riod;
• the device is beyond repair.
Attention! The manufacturer reserves the right without notice to
change the design of the instrument and software without compro-
mising existing features.

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Certicate of Acceptance
“DETA-AP-13” device Serial No.
produced and accepted in accordance with mandatory require-
ments of state standards and technical documentation in eect
and established as t for use
Technical control mark:
seal
(signature) (name)
201
(date of issue)

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COUNTERFOIL No. 1 for warranty repairs to device “DETA-AP-13” Withdrawn 201 , Repairs undertaken by (name, signature)
ELIS Research & Development Enterprise LLC
4 oce 2408, Savelkinskiy Pr., Zelenograd
Moscow Russia, 124482
Tel.: [phone]
Coupon No. 1 for warranty repairs to the device
“DETA-AP-13”
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)

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COUNTERFOIL No. 2 for warranty repairs to device “DETA-AP-13” Withdrawn 201 , Repairs undertaken by (name, signature)
ELIS Research & Development Enterprise LLC
4 oce 2408, Savelkinskiy Pr., Zelenograd
Moscow Russia, 124482
Tel.: [phone]
Coupon No. 2 for warranty repairs to the device
“DETA-AP-13”
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)

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17
COUNTERFOIL No. 3 for warranty repairs to device “DETA-AP-13” Withdrawn 201 , Repairs undertaken by (name, signature)
ELIS Research & Development Enterprise LLC
4 oce 2408, Savelkinskiy Pr., Zelenograd
Moscow Russia, 124482
Tel.: [phone]
Coupon No. 3 for warranty repairs to the device
“DETA-AP-13”
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)

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4 oce 2408, Savelkinskiy Pr., Zelenograd, Moscow, Russia, 124482
Tel.: [phone]
e-mail: [e-mail]
www.deta-elis.ru
MISSION TO CURE
4 oce 2408, Savelkinskiy Pr., Zelenograd, Moscow, Russia, 124482
Tel.: [phone]
e-mail: [email protected]
www.deta-elis.ru