【逸美EME是哪个国家的品牌？】

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EME逸美是一种采用专利技术生产的高支撑力的注射型溶液，主要成分为透明质酸、羟丙基甲基纤维素、平衡盐溶液。它将大分子量透明质酸通过第三代交联技术整合在纤维素骨架上，注射到皮下后起塑形、填充和补水作用。

EME逸美--透明质酸类注射填充产品革命性的飞跃(国家药监局注册证，注册号:国食药监械(准)字号2009第3460746号,有效期至2013年10月10日)

EME逸美是一种丰盈及高支撑力的注射型凝胶，由透明质酸(Hyaluronicacid)制造而成。

EME逸美注射产品由加拿大EMELAB技术开发，由北京爱美客生物科技有限公司生产出品。EME逸美专业注射系列产品于2009年10月获国家SFDA正式批准上市，因产品高度安全及有效，被卫生部国家食品药品监督管理局正式认证批准，适用于面部多部位的透明质酸注射产品。

2006年EME通过国家食品药品监督管理局济南医疗器械监督检验中心检验;

2007年EME通过北京市药品监督管理局的质量体系考核;

2008年EME通过国家食品药品监督管理局技术审评专家组审评;

2009年EME通过国家食品药品监督管理局组织的GMP认证中心专家在内的专家组联合检查验收;

2009年EME获中国SFDA批准，适用于面部多部位的透明质酸注射产品。

英文翻译：EME is a kind of injection solution with high supporting force, which is produced by patent technology. Its main components are hyaluronic acid, hydroxypropylmethylcellulose and balance salt solution. It integrates the high molecular weight hyaluronic acid on the cellulose skeleton through the third generation cross-linking technology, and plays the role of shaping, filling and water replenishing after injection into the subcutaneous. EME Yimei - a revolutionary leap of hyaluronic acid injection filling products (registration certificate of the State Administration of drug administration, Registration No. 2009, No. 3460746th of the national food and drug administration, which is valid until October 10, 2013) EME Yimei is an injection gel with abundant and high supporting force, made of hyaluronic acid (Hyaluronicacid). EME Yimei injection products are developed by Canadian emelab technology and produced by Beijing aimec Biotechnology Co., Ltd. EME Yimei professional injection series products were officially approved by SFDA in October 2009. Due to the high safety and effectiveness of the products, it was officially certified and approved by the State Food and Drug Administration of the Ministry of health, which is applicable to the hyaluronic acid injection products in multiple parts of the face. In 2006, EME passed the inspection of Jinan medical device supervision and inspection center of State Food and drug administration; in 2007, EME passed the quality system assessment of Beijing Drug Administration; in 2008, EME passed the review of technical review expert group of State Food and drug administration; In 2009, EME passed the joint inspection and acceptance of expert groups including GMP Certification Center experts organized by the State Food and drug administration; in 2009, EME was approved by China SFDA, which is suitable for hyaluronic acid injection products of multiple parts of the face.

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