Table of contents Introduction Explanation of symbols Description of the device structure Device setup Warnings Contraindications and recommendations Technical details Warranty Incident application form USER GUIDE V.2.0.R2...
Wishing you satisfaction of DRACO usage, we thank you for your choice. DRACO device is a response for the patients need who are suffering from crurotalar joint disfunctions. Due to its adaptavity it enables to perform independent movements: flexion, extension, abduction, adduction and multidimensional movement of the foot.
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 exploatation warnings. Unless follwed, may result in minor personal injury and/or product/property damage.
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3. DESCTIPTION OF THE DEVICE STRUCTURE Versatility of DRACO 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.2.0.R2...
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The list of components: Element Description Ammount Adaptive element that enables to perform self-assisted exercised of the Lever crurotalar joint. The lever can be separated through unscrewing the knob (2). Knob V.1 A knob enabling the lever installation (1) in the structure of the device. A knob that locks/unlocks the option of flextion and extension of the crurotalar Knob H.1 joint exercises.
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. Visualisations below advice how to perform a chosen technique of rehabilitation. 4.1.
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4.2. Abduction and adduction of the crurotalar joint. A knob H.1 (3) locked. A knob H.2 (4) unlocked. Weight (5) placed in the sockets according to the therapist indications (to support the resistance exercies). Lever (1) installed according to the therapist indications (used to perform self-assisted exercises). ...
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(9)). Therapeutic process realized with usage of DRACO device is performer in sitting. The patient must be comforted while seated, with possibility to adjust the height of the seat.
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 DRACO 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.
16 kg 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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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.
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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