总胆红素测定试剂盒(钒酸盐氧化法)
注册证编号
浙食药监械(准)字2012第2400312号
型号规格
仪器:日立7180型适用包装规格:R1:40ml×1 R2:10ml×1; R1:60ml×1 R2:15ml×1;R1:60ml×2R2:15ml×2; R1:80ml×2 R2:20ml×2;R1:60ml×3R2:45ml×1。仪器:奥林帕斯AU2700型适用包装规格:R1:40ml×1 R2:10ml×1; R1:60ml×1 R2:15ml×1;R1:60ml×2 R2:15ml×2; R1:80ml×2 R2:20ml×2;R1:60ml×3 R2:45ml×1。仪器:贝克曼DX800型适用包装规格:R1:40ml×1 R2:10ml×1; R1:60ml×1R2:15ml×1;R1:60ml×2 R2:15ml×2; R1:80ml×2R2:20ml×2。仪器:雅培C16000型适用包装规格:R1:40ml×1 R2:10ml×1; R1:60ml×1 R2:15ml×1;R1:60ml×2 R2:15ml×2; R1:80ml×2 R2:20ml×2;R1:50ml×4 R2:50ml×1。仪器:科华卓越330型适用包装规格:R1:40ml×1 R2:10ml×1; R1:60ml×1R2:15ml×1;R1:60ml×2 R2:15ml×2; R1:80ml×2R2:20ml×2;R1:80ml×4 R2:80ml×1。
结构及组成
R1:酒石酸缓冲液PH7.0 、表面活性剂R2:偏钒酸盐产品储存条件及有效期:原包装试剂盒在2-8℃避光条件下可稳定12个月。
适用范围
本试剂盒用于体外定量测定人体血清中总胆红素的含量。
备注
1、原注册证有效期至2016年7月10日止;2、包装规格由“R1:40ml×1、R2:10ml×1,R1:60ml×1、R2:15ml×1,R1:60ml×2、R2:15ml×2,R1:80ml×2、R2:20ml×2,R1:80ml×4、R2:80ml×1”变更为“R1:40ml×1、R2:10ml×1,R1:60ml×1、R2:15ml×1,R1:60ml×2、R2:15ml×2,R1:80ml×2、R2:20ml×2,R1:80ml×4、R2:80ml×1,R1:60ml×3、R2:45ml×1,R1:50ml×4、R2:50ml×1”。3、注册产品标准由YZB/浙3202-2012变更为YZB/浙3202-2015。申请人根据批准变更内容自行修订说明书和标签。变更情况:1、包装规格由“R1:40ml×1、R2:10ml×1,R1:60ml×1、R2:15ml×1,R1:60ml×2、R2:15ml×2,R1:80ml×2、R2:20ml×2,R1:80ml×4、R2:80ml×1”变更为“R1:40ml×1、R2:10ml×1,R1:60ml×1、R2:15ml。
注:器械注册证相关信息来源国家药品监督管理局(数据具有延迟性)