Table of contents Introduction Explanation of symbols Description of the device structure Device setup Warnings Contraindications and recommendations Warranty Incident application form USER GUIDE V.0.2.R2...
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.
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.
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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. USER GUIDE V.0.2.R2...
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The list of components: Adaptive element that enables to perform self-assisted exercised of the Lever crurotalar and knee joint. External frame Base element enabling to attach other components. Clamp lever 1,2,3 Clamp elements enabling to define the position of the shin stabilization (6). Foot platform Foot positioning element.
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.
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4.2. Flexion and extension of the crurotalar joint: Abduction and adduction knob (9) locked, (10) locked, Reciprocating movement knob Mounting pins (6) off, Shin stabilization (8) installed (clamp levers (3) closed). USER GUIDE V.0.2.R2...
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4.3. Abduction and adduction of the crurotalar joint: (9) unlocked, Abduction and adduction knob (10) locked, Reciprocating movement knob Mounting pins (6) installed, Shin stabilization (8) installed (clamp levers (3) closed). USER GUIDE V.0.2.R2...
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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).
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.
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.
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7. TECHNICAL DETAILS Manufacturer: Terma Sp. z o.o. Model: AVIOR Version: V.1.0 Class: Class I, Rule I Dimensions: Ranges: Abduction and adduction in the crurotalar joint 40° Flexion and extension of the crurotalar joint: A = 810 mm 35° B = 410 mm...
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.
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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.
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 termamed@termamed.pl to the manufacturer by e-mail or posted.
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