注册证编号 | 皖械注准20172400074 [查看相关产品信息] |
注册人名称 | 安徽大千生物工程有限公司[查看公司信息] |
注册人住所 | 合肥市经开区桃花工业园繁华大道工投·立恒工业广场B12C |
生产地址 | 合肥市经开区桃花工业园繁华大道工投·立恒工业广场B12C |
产品名称 | 髓过氧化物酶测定试剂盒(免疫比浊法) |
管理类别 | 第二类 |
型号规格 | R1:1×15ml、R2:1×5ml;R1:1×30ml、R2:1×10ml;R1:1×45ml、R2:1×15ml;R1:1×60ml、R2:1×20ml;R1:2×30ml、R2:2×10ml;R1:1×20ml、R2:1×5ml;R1:1×40ml、R2:1×10ml;R1:1×60ml、R2:1×15ml;R1:1×65ml、R2:1×15ml;R1:2×65ml、R2:2×15ml;R1:2×60ml、R2:1×30ml;R1:2×50ml、R2:1×25ml;R1:2×45ml、R2:1×30ml;R1:2×60ml、R2:2×15ml;R1:4×50ml、R2:1×45ml;R1:1×16ml、R2:1×3.5ml(60测试);R1:5×16ml、R2:5×3.5ml(300测试);R1:1×750ml、R2:1×250ml。 |
结构及组成/主要组成成分 | R1: 缓冲液、聚乙二醇 R2: 缓冲液、髓过氧化物酶抗体胶乳颗粒 校准液、质控品:髓过氧化物酶(可选) |
适用范围/预期用途 | 适用于体外定量测定人血清中髓过氧化物酶抗体胶乳颗粒(MPO)的含量。 |
审批部门 | 安徽省药品监督管理局 |
批准日期 | 2022/1/17 |
生效日期 | 2022/1/17 |
有效期至 | 2027/8/6 |