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Triomed UNIVERSAL User Manual

Triomed UNIVERSAL
32 pages
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ACTIVE MEDICAL DEVICE
FOR STIMULATION BY ELECTROMAGNETIC FIELD
USER MANUAL
TRIOMED UNIVERSAL
Version 3
Introduced on 20.03.2015
Tallinn 2015
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Triomed UNIVERSAL Specifications

General IconGeneral
CategoryMedical Equipment
UsageClinical use
CompatibilityCompatible with standard medical interfaces
MaterialMedical-grade materials
SterilitySterile or sterilizable depending on application
Regulatory ComplianceComplies with applicable medical device regulations

Summary

1. PURPOSE

2. MECHANISMS OF THERAPEUTIC EFFECTS

2.1. General mechanisms of action

Explains how millimeter and infrared radiation affect biological tissues, activating metabolism and regulating functions.

2.2. Mechanisms of specialised action of MM radiation

3. INDICATIONS AND CONTRAINDICATIONS FOR USE

3.1. Indications

Lists various conditions like colds, heart failure, hypertension, neurological diseases, etc., for which the device is indicated.

3.2. Contraindications:

3.3. Recommendations for using external radiators

4. TECHNICAL AND OPERATIONAL CHARACTERISTICS

4.1. General technical characteristics

Details compliance with directives, device classification (Class IIa), and its main components like generator and radiators.

4.2. Structure and functioning

5. PACKAGE CONTENTS

6. LABELLING

7. PACKAGING

8. DISPOSAL

9. WARRANTY

10. PREPARING THE DEVICE FOR USE

10.1. Operating restrictions

Lists forbidden actions like using the device without the manual, faulty device, in high humidity, or with improper handling.

IT IS NOT RECOMMENDED

Advises against using R06 saline batteries due to limited resource and potential damage, recommending LR06 instead.

10.2. Safety precautions

Mentions no special precautions for patients during failure/evacuation, comfortable positions, and using the storage bag.

10.3. Preparing the device for use

Instructs to inspect the device for damage before use and details battery replacement procedure and indicator meanings.

CHECKING OF THE SERVICEABILITY OF THE DEVICE:

10.4. List of possible faults and suggested remedies

10.5. Technical maintenance

11. PROCEDURE FOR USING THE DEVICE

11.1. Selecting the impact position

Guides on selecting stimulation areas like pathological focus, organ projection zones, biologically active points, and spinal column.

11.2. Local stimulation in the pathological focus

Details how to perform local stimulation on surface pathological foci, recommending frequency and duration for initial stages.

11.3. Use of device in Head zones

Explains the link between spinal cord segments and internal organs, and how Head zones facilitate therapeutic effects on damaged organs.

11.4. Stimulation of biologically active zones

Describes stimulating the collar area, lower thoracic/lumbar areas, and their effects on vascular system, brain, pituitary, thyroid, kidneys, and adrenal glands.

11.6. Stimulation of reflexogenic zones

Identifies other reflexogenic zones like palm, foot, nasal region, auricle, and cranial integuments for stimulation.

11.7. Treatment description

Details patient position, radiator selection, connection, and placement on the body with the colour label facing up.

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