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Sunmax Collagen Implant I-Plus

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Sunmax collagen implant i-plus is a sterile injectable device composed of cross-linked highly purified spf (specific pathogen free) porcine dermal collagen that is purified through several advanced purification process. The final collagen implant product has been sterile filtered and filled in a single use syringe, which is then packaged with a sterile needle under a sterile condition. -- composition each syringe contains 35 mg/ml purified cross-linked collagen. -- functions for correction of facial defects and soft tissue augmentation. -- mode of action sunmax collagen implant i-plus is mainly composed of type i atelocollagen. After injection, the suspended collagen bears appropriate protease resistance and therefore can slow down the degradation. The implant forms a soft cohesive network of fiber, which is responsible for restoring contour for a long time. Over a period of months, the implant is colonized by host connective tissue cells; once established, the implant takes on the texture and appearance of normal host tissue and is subjected to the same stress and ageing processes. -- direction for use 1. Prior to the treatment of sunmax collagen implant i-plus, the patient should be fully informed of the indications, contraindications, warnings, precaution, possible adverse events and method of administration. 2. In order to prevent inflammation and infection, hygienic and aseptic conditions must be observed. The area to be treated should be washed and swabbed with alcohol or other antiseptics. 3. Sunmax collagen implant i-plus is implanted intradermally through a 27~30 gauge of sterile needle. The needle should be placed into the plane(s) of apparent deformity at 10~25 degree angle. 4. If blanching is not achieved, withdraw the needle immediately as it has probably been placed too deeply in the dermis. 5. Avoid injecting sunmax collagen implant i-plus into blood vessels as collagen can initiate platelet aggregation and may cause vascular occlusion and


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