TERMA AVIOR User manual

USER GUIDE
V.0.2.R2

USER GUIDE
V.0.2.R2
AVIOR
USER GUIDE
V.0.2.R2

USER GUIDE
V.0.2.R2

USER GUIDE
V.0.2.R2
Table of contents
1. Introduction 3
2. Explanation of symbols 4
3. Description of the device structure 5
4. Device setup 7
5. Warnings 14
6. Contraindications and recommendations 15
7. Warranty 17
8. Incident application form 19

USER GUIDE
V.0.2.R2
1. INTRODUCTION
Wishing you satisfaction of AVIOR usage, we thank you for your choice.
AVIOR device is a response for the patients who are suffering from crurotalar and knee joint disfunctions Due to
its adaptavity it enables to perform independent movements: flexion, extension, abduction, adduction and
multidimensional movement of the foot and also flexion and extension of the knee. Construction of AVIOR device
enables the complex crurotalar and knee joint rehabilitation based on self-assisted, active and resistance
exercises.
This manual provides all the needed information concerning AVIOR device proper functioning.
The manufacturer is entitled to change the content of the manual when it’s needed. The updated version of the
manual will be available to download from the manufacturer's website www.termamed.pl from the "Downloads"
section.
Manufacturer:
Terma Sp. z o.o.
80-298 Gdansk
Czaple 100
Poland
T: [phone]
F: [phone]
email: [email protected]
www.termamed.pl

USER GUIDE
V.0.2.R2
2. EXPLANATIONS OF SYMBOLS
It is mandatory to read the safety statements before using the device. The safety statements are classified as
follows:
Safety warnings and essential usage details.
Safety of exploitation warnings. Unless followed, may result in minor personal injury and/or
product/property damage.
Mark of the active part of the device described on the illustrated scheme and explained in
table.

USER GUIDE
V.0.2.R2
3. DESCTIPTION OF THE DEVICE STRUCTURE
Versatility of AVIOR possible settings enables to perform the therapy of various disfunctions of crurotalar joint.
The structure of the device is explained on the model below.
6
3
5
2
1
8
10
12
9
11
4
7

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V.0.2.R2
The list of components:
1
Lever
Adaptive element that enables to perform self-assisted exercised of the
crurotalar and knee joint.
2
External frame
Base element enabling to attach other components.
3
Clamp lever 1,2,3
Clamp elements enabling to define the position of the shin stabilization (6).
4
Foot platform
Foot positioning element.
5
Transport handle
Handle that enables safe and comfortable transportation of the device info
needed room.
6
Mounting pin
Adaptive element which installed in the lever (1) or external frame (2)
enables to perform exercises of the knee joint. When the mointing pin is
removed, exercises of the crurotalar joint can be performed.
7
Main frame
Base element that enables to attach other components.
8
Shin stabilization
Shin stabilisation positioning element.
9
Abduction and adduction
knob
Clamps defining the position of the foot platform against the saggital axis of
the device.
10
Reciprocating movement
lock
Clamps defining the position of the foot platform against the rail.
11
Wheel
Element that enables safe and comfortable transportation of the device info
needed room.
12
Adjustable mounting
element
Positioning element with possibility to adjust the height of the shin
stabilization in the structure of the device. This element is compatible with
the shin stabilization (8).
13
Expanders
Weight defining elements enabling to perform resistance exercises (not
mentioned on the model).

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V.0.2.R2
4. Device set up
The device reaches the Customer folded. It needs to attach the lever (1) to the main frame (6) using the knob V.1
(2) which is described on the page 5.
Visualizations below advice how to perform a chosen technique of rehabilitation.
4.1. Flexion and extension of the knee:
Abduction and adduction knob locked (9),
Reciprocating movement knob (10) unocked,
Mounting pins (6) installed,
Shin stabilization (8) removed.

USER GUIDE
V.0.2.R2
4.2. Flexion and extension of the crurotalar joint:
Abduction and adduction knob (9) locked,
Reciprocating movement knob (10) locked,
Mounting pins (6) off,
Shin stabilization (8) installed (clamp levers (3) closed).

USER GUIDE
V.0.2.R2
4.3. Abduction and adduction of the crurotalar joint:
Abduction and adduction knob (9) unlocked,
Reciprocating movement knob (10) locked,
Mounting pins (6) installed,
Shin stabilization (8) installed (clamp levers (3) closed).

USER GUIDE
V.0.2.R2
4.4. Expanders installation.
To perform resistance exercises expanders need to be installed. They are attached to the device as one
of components.
Expanders installation to perform flexion
and extension of the knee joint:
Expanders need to be installed in the
dedicated sockets in the main frame (7).
Pay attention to the proper location of the
expanders, which should slide into the
space of the smaller hole.
Expanders installation to perform
abduction and adduction of the crurotalar
joint:
Expanders need to be installed in the
dedicated sockets in the foot platform (4).
The sleeve at the end of the expander
must fit the wider hole. Slide the sleeve to
the space of the smaller hole.
Expanders installation to perform flexion
and extension/abduction and adduction of
the crurotalar joint:
Attach the expanders to the sockets in the
main frame (2). Pay attention to the
proper location of the expanders, which
should slide into the space of the smaller
hole.

USER GUIDE
V.0.2.R2
5. WARNINGS
To ensure the highest safety of user’s health it is necessary to read and follow the warnings below.
Therapeutic process realized with usage of AVIOR device is performer in sitting. The patient must be
comforted while seated, with possibility to adjust the height of the seat.
It is advised that the angle between a thigh and shin was nearly 90° while the thigh is placed in parallel
to the ground.
Before usage it is necessary to read the user guide first and definitely follow the terms, advices and
warnings.
User guide is also available at www.termamed.pl where tutorial videos are also uploaded.
The only entity allowed to service and technical reviews is a manufacturer TERMA Sp. z o.o. of a
service pointed by a manufacturer. The manufacturer is not responsible for any improvement or
repairs made by other parties.
In case of any incidents which causes damage on the patient’s health, it must be reported
immediately to the manufacturer. Additionaly, it’s advised to fill in such case “Incident aplication form”
and send it by post or e-mail to the manufacturer. The form is a part of a user guide available also at
www.termamed.pl in the “Downloads” section.
The platform of the foot and shin stabilization are equipped with belts fastening the foot in the structure
of the device. Before the exercises are performed, the foot must be stabilized in the device.

USER GUIDE
V.0.2.R2
6. CONTRAINDICATIONS AND RECOMMENDATIONS
In order to ensure the highest comfort and safety during AVIOR device exploitation, please mention the
contraindications to the therapy listed below:
1. Changes in the skeletal system, such as: unfused bones, injuries which do not allow for the implementation of
the training.
2. If the patient anthropometric conditions do not allow for adjustment of the structure of the device.
It is recommended to use sportswear made of cotton for full range of motion.

USER GUIDE
V.0.2.R2
Abduction and adduction in the crurotalar joint:
40°
Flexion and extension of the crurotalar joint:
35°
7. TECHNICAL DETAILS
Manufacturer:
Model:
Version:
Class:
Dimensions:
Weight:
Terma Sp. z o.o.
AVIOR
V.1.0
Class I, Rule I
A
B
C
A = 810 mm
B = 410 mm
C = 1020
mm
25 kg
Ranges:

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V.0.2.R2
8. WARRANTY
Terma Sp. z o.o. guarantees good condition and efficient operation of the device mentioned in the Warranty Card,
hereinafter referred to as Product, according to the technical and exploitation details described in the user guide.
Warranty confirms the reponsibility of the entity who introduced the product to the market to free of charge
removal of any faults of the product that was sold. The warranty does not limit or suspend buyer’s rights resulting
from nonconformity of the goods with the contract.
1. The warranty period starts on the day of receipt of the Product and is 24 months for the main structure of
the device.
2. The free warranty repair shall be understood as the performance by the Guarantor during the warranty
period of the specific activity appropriate for removing the defect covered by the warranty. This warranty
covers Product defects caused by defective parts or defects in production. Warranty liability covers only
defects caused by the underlying causes of the sale.
3. The condition for the Buyer to use the rights given by warranty is to present at the time of the service
request a total of:
a. Deffective product,
b. A proof of purchase.
4. The warranty will be done by the service during 14 working days from the date of acceptance the
product to be repaired or from delivering it to the manufacturer's service to the address:
Terma Sp. z o.o.
Czaple 100, 80-298 Gdańsk, Poland
58 694 06 04, serwis-me[email protected]l
5. The scope of warranty service does not cover the installation, commission and maintenance activities
which, in accordance with the user guide, is required to performed by the user of the Product on his own.
Warranty repairs do not include periodic maintenance and product reviews, and in particular: cleaning,
regulation, performance control, correction of operating errors or parameter programming, and other actions
that the user is responsible for.
The warranty excludes cases of random damage independent of operating conditions (for example: thefts,
accidents, fires, floods) and mechanical damage caused by improper use.
6. The Buyer, by submitting the Product to the Service, and in particular by sending it to third parties, shall
provide him with a secure package. Any damage or damage to the Product resulting from its improper
packaging shall be covered by the Buyer. Along with the Product, the Buyer shall include the exact
description of the defect that causes the need of repair. The person submitting the complaint should
provide his / her personal details: name, address, telephone number.
7. Guarantor chooses the best way to remove the defect. The Guarantor undertakes to remove physical
defects free of charge by repair or replacement of the Product free of defects. Regardless of how defects
are removed, the warranty continues.
8. Any faulty Products or parts exchanged under the guarantee become the property of Terma Sp. o.o.
9. If only a part of the Product is defective and can be detached from the Product in accordance with the
technical and operating conditions described in the user guide, the Buyer's right under these Warranty
Terms shall be limited to the repair of the defective part of the Product only.
10. The Buyer has the right to exchange the Product for the new one, free from defects, if:
a. During the warranty period referred to in Section 1, the Service will carry out five warranty
repairs and the Product will still reveal defects that prevent it from being used for its intended
purpose, or
b. The service will confirm in writing that removal of the defect is impossible.
11. User loses warranty rights in case of:

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V.0.2.R2
a. Statements of unauthorized alerts or corrections in the Guarantee Card made by unauthorized
entities.
b. Statements made in the Product by unauthorized modifications or adjustments not expressly
provided in the operating instructions.
c. Statements of attempted repairs and interventions by third parties.
d. Statements of use of parts and materials not recommended by the Manufacturer and the
Guarantor.
12. The warranty does not support:
a. Damages caused by improper storage, transportation, failure to perform maintenance, periodic
inspection.
b. Damages resulting from maintenance and repair work performed by the user in contravention of
the user guide.
c. Damages caused by the user's fault or ignorance.
d. Product damages resulting from natural usage resulting from its use.
e. Damage caused by the user's fault or ignorance.
f. Damages caused by non-original spare parts or use of materials not intended for use with the
Product.
g. Products whose Warranty Card or serial numbers have been altered, blurred or removed in any
way.
13. Warranty does not cover parts and materials whose consumption is a natural consequence of work, and
these are, in particular, consumable items that are clearly consumed during the operation of the Product.
Warranty rights do not include the buyer's right to demand the return of the lost profits in connection with
the failure and repair of the Product.

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V.0.2.R2
INCIDENT APPLICATION FORM
In the event of an incident that results in damage to the equipment or injury to the patient, manufacturer
must be immediately reported. After filling the "Incident application form," given below, it should be provided
to the manufacturer by e-mail term[email protected] or posted.
Name of institution:
Adress:
Institution contact details:
Contact details of the patient involved in the incident:
Contact person name, surname, e-mail and phone number:
Date of the incident:
Date of the notification:
Description of the incident:
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Incident effects:
Additional informations:
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