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MD-SHOULDER Description Useful medical device for improving joint mobility of the shoulder and upper limb, whose main therapeutic treatment consists of the following functions: 1. Barrier effect. 2. Lubricating activity. 3. Mechanical support in case of continuous drug therapy. The use of MD-SHOULDER is recommended by qualified medical personnel in private or public healthcare facilities for: - improves mobility of the shoulder joint and upper limb; - promotes muscle relaxation; - supports muscle structures; - relieves localized pain and pain caused by movement. How to use MD-SHOULDER 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-SHOULDER can be combined with MD-NEURAL, MD-POLY and MD-MUSCLE (one or more of these). Additionally, in cases where tissue matrix support therapy is required or where a slowdown in physiological aging is required, MD-SHOULDER can be combined with MD-MATRIX and MD-TISSUE. Therapeutic protocol : 1-2 treatments per week, for 10 consecutive weeks. Method of administration: periarticular injection (the application area must be aseptic; the needle is inserted close to the joint 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. Method of administration: intraarticular injection. For this use of the medical device, the following materials and accessories are recommended: • Materials to ensure aseptic conditions of the skin: disposable gloves, iodine solution, alcohol solution, sterile gauze, ethyl chloride skin spray. It is recommended to apply a local anesthetic to the treated skin. • Needles: sterile 22 G. • Syringes: 5 or 10 cc, depending on the amount of solution to be injected. - Intra-articular injection of the shoulder, anterior aspect: The patients hand rests on the thigh, while the shoulder muscles are relaxed. The glenohumeral joint can be palpated with the fingers between the coracoid process and the humeral head. Because the shoulder is in internal rotation, the humeral head can be palpated as it rotates inward, and the joint space can be felt as a depression located lateral to the coracoid process. Insert a 22-gauge needle lateral to the coracoid process. Direct the needle into the joint space. - Intra-articular injection treatment of the shoulder, posterior aspect: The posterior aspect of the shoulder joint can be identified by rotating the patients arm. This position can be achieved by placing the patients ipsilateral hand on the contralateral shoulder. The humeral head can be palpated by placing a finger posteriorly on the acromion while the shoulder is rotated. Insert a 22-gauge needle approximately 1 cm inferior to the posterior tip of the acromion and direct it anteriorly and medially. components Collagen of porcine origin. Excipients: Iris, NaCl, water for injections. warnings Disposable. No cases of hypersensitivity to MD-SHOULDER have been reported. Contains animal collagen from porcine species. Patients with known hypersensitivity to the component or excipients should first undergo a test injection in the arm and be observed for one hour. Shoulder pain requires differential diagnosis with chronic cervical syndrome, ischemic heart disease (acute/chronic, left shoulder only), cholecystitis/cholelithiasis (right shoulder only), cervicobrachialgia, and trapezius muscle trigger point. 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 MD10
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