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东软威特曼生物科技(南京)有限公司

境内医疗器械(注册) — “苏械注准20172400211”基本信息
注册证编号苏械注准20172400211 [查看相关产品信息]
注册人名称东软威特曼生物科技(南京)有限公司[查看公司信息]
注册人住所南京市雨花台区西善桥南路108号2号楼
生产地址南京市雨花台区西善桥南路108号2号楼
产品名称低密度脂蛋白胆固醇检测试剂盒(终点法)
管理类别第二类
型号规格80mL/盒(R1:1×60mL、R2:1×20mL;R1:2×30mL、R2:1×20mL)100mL/盒(R1:1×75mL、R2:1×25mL;R1:2×37.5mL、R2:1×25mL;R1:3×25mL、 R2:2×12.5mL); 160mL/盒(R1:2×60mL、R2:2×20mL;R1:3×40mL、R2:2×20mL);200mL/盒(R1:2×75mL、R2:2×25mL;R1:3×50mL、R2:1×50mL;R1:4×37.5mL、R2:2× 25mL;R1:3×50mL、R2:2×25mL;R1:2×75mL、R2:1×50mL;R1:6×25mL、 R2:4×12.5mL)240mL/盒(R1:5×36mL、R2:3×20mL;R1:4×45mL、R2:3×20mL; R1:3×60mL、 R2:3×20mL) 300mL/盒(R1:3×75mL、R2:3×25mL;R1:5×45mL、R2:3×25mL;R1:5×45mL、 R2:2×37.5mL;R1:6×37.5mL、R2:3×25mL;R1:3×75mL、R2:1×75mL)
结构及组成/主要组成成分试剂1:两性离子缓冲溶液(Good’s缓冲液)53.6mmol/L pH6.5,表面活性剂:聚氧乙烯亚烷基苯基醚 4.2g/L。试剂2:胆固醇酯酶2000 U/L,胆固醇氧化酶2000 U/L,过氧化物酶3000 U/L。 注:不同批号之间的各组分不可以互换。
适用范围/预期用途用于人血清中低密度脂蛋白胆固醇含量的体外定量测定。
审批部门江苏省药品监督管理局
批准日期2021/11/28
生效日期2021/11/28
有效期至2027/2/23
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