型号规格
R1:1×20ml,R2:1×4ml;R1:1×40ml,R2:1×8ml;R1:1×50ml,R2:1×10ml;R1:1×60ml,R2:1×12ml;R1:1×70ml,R2:1×14ml;R1:1×80ml,R2:1×16ml;R1:2×50ml,R2:1×20ml;R1:2×60ml,R2:2×12ml;R1:2×80ml,R2:2×16ml;R1:3×40ml,R2:3×8ml;R1:3×50ml,R2:3×10ml;R1:3×60ml,R2:3×12ml;R1:3×80ml,R2:3×16ml;R1:4×40ml,R2:4×8ml;R1:4×50ml,R2:4×10ml;R1:4×60ml,R2:4×12ml;R1:4×80ml,R2:4×16ml;R1:6×20ml,R2:6×4ml;R1:6×40ml,R2:6×8ml;R1:6×50ml,R2:6×10ml;R1:6×60ml,R2:6×12ml;R1:6×80ml,R2:6×16ml;西门子测试数:200测试/盒(R1:1×50ml,R2:1×10ml)
变更情况
注册人住所、生产地址由“上海市闵行区联航路1588号1幢软件孵化大楼1#楼301、302室”变更为“上海市闵行区三鲁公路3279号1幢1号楼3层、4层”。;本文件与“沪械注准20162400080”注册证共同使用。;2017-09-05,1、医疗器械注册证变更内容,增加包装规格和试剂配套校准品等,详见附件1(共1页)。
2、产品技术要求变更内容,增加校准品的性能指标等,详见附件2(共15页)。
3、产品说明书变更内容,增加试剂配套校准品和适用机型等,详见附件3(共3页)。;本文件与“沪械注准20162400080”注册证共同使用。;2021-11-01