ALMAG-01
Operating manual Page 3
Dear customer!
You have got "ALMAG-01" Portable Magnetotherapy Device with a Travelling
Pulsed Field (further mentioned as ALMAG) intended to be used for treatment and
prophylaxis of a wide spectrum of diseases in the conditions of physiotherapy
departments, patient care and prophylactic institutions and the patient himself in home
conditions on doctor`s advice . Taking the procedure with the help of ALMAG on the
doctor`s advice you should follow recommended therapeutic technique given in operating
manual to the device.
ALMAG is belonged to the products of medical devices and it is included in the
nomenclature of physiotherapeutic devices allowed for application in medical practice. RF
Public Health Ministry Committee for new medical apparatus Minutes No. 7 of
9.08.1999. The registration certificate No.FS 022a0409 / 1024–04 of 14.12. 2004.
ATTENTION! Operating manual should be both carefully studied prior to the first
application of the Device and followed strictly in the process of its operation. This will
assure the device correct and safety operation. When being passed to a third man the
Operating Manual should be enclosed to the Device..
The present Operating Manual is a document proving the basic parameters and
technical characteristics of ALMAG Device.
When purchasing a Device make sure of the seller's signature or merchandiser's stamp
as well as of the sales date.
1. PURPOSE OF THE DEVICE
1.1 General information
1
.
1.1 The Device is designed to produce a therapeutic effect on the human body with a
travelling pulsed magnetic field and can be applied both at physiotherapeutic departments
of patient care and prophylactic institutions and by a patient himself at home conditions.
1.1.2 The Device is to be sold either through retail or wholesale trading network..
1.1.3 The Device is designed to operate under normal environmental conditions for
Temperate Cold climate design products, ambient temperature b10°C - +35°C,
atmospheric pressure from 86,6 kPa to 106,7 kPa (650 - 600 mmHg).
1.1.4 Electric safety class of the Device: Class II of B type according to IEC 601-1-2-
93.