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MD-THORACIC Description Useful medical device for improving the mobility of the thoracic vertebrae, whose main therapeutic treatment consists of the following functions: 1. Barrier effect. 2. Lubricating activity. 3. Mechanical support in case of continuous drug therapy. MD-THORACIC is recommended for use by qualified medical personnel in private or public healthcare facilities for: - improves the mobility of the thoracic spine; - promotes muscle relaxation; - supports muscle structures in postural disorders; - relieves localized pain and pain caused by movement and postural errors. How to use MD-THORACIC can be used alone or in combination with other medical devices from the same line, to guarantee personalized treatment according to the individual clinical picture. In cases where supportive treatment is required for the onset of acute pain, MD-THORACIC can be combined with MD-NEURAL, MD-POLY and MD-MUSCLE (one or more of these). In addition, in cases where tissue matrix support therapy is required or where a slowdown of physiological aging is required, MD-THORACIC can be combined with MD-MATRIX and MD-TISSUE. Periarticular therapeutic protocol : 2 treatments in the first 2 weeks; then 1 treatment until symptoms improve (on average 8-10 sessions). For chronic conditions: continue with 1 treatment per week for a month until symptoms improve, then with 1 treatment per month. The application area should be aseptic; insert the needle close to the joints to a depth of 2-4 mm. For this use of the medical device, the following materials and accessories are recommended: • Material to ensure skin asepsis: disposable glove, iodine-based solution, alcohol-based solution, sterile gauze, ethyl chloride-based skin spray. • Needles: sterile 27 G. • Syringes: 5 or 10 cc, depending on the amount of solution to be injected. components Collagen of porcine origin. Excipients: Cimcifuga, NaCl, water for injections. warnings Disposable. No cases of hypersensitivity to MD-THORACIC have been reported. Contains porcine collagen. Patients with known hypersensitivity to the component or excipients should first undergo a skin prick test and be observed for one hour. Back pain requires differential diagnosis with pain secondary to primary or metastatic tumors; reflected and referred pain originating in the viscera. Slight redness at the injection site may be caused by the mechanical effect of the needle or a skin reaction. Application may cause symptoms of burning/pain at the injection sites, which generally disappear within 5-10 minutes after the end of treatment. Skin cleansing/disinfection is necessary before and after application. Any pyogenic bacteria could cause an abscess at the injection site. Keep out of the reach and sight of children. Do not use after expiration. Use the product immediately after opening. Do not use if seal is broken or tampered with. After opening, the contents of the vial should be injected immediately. Do not use if packaging is damaged. Conservation Store between 2°C and 30°C, away from sunlight and frost. The expiration date refers to the product in its intact packaging, stored correctly. Format Pack of 10 sterile 2 ml vials. Code MD12
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