发布时间:2024-05-27 17:49:26 - 更新时间:2024年06月29日 15:22
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本标准规定了凝血酶时间检测试剂(盒)质量检验测试的通用技术要求,包括术语和定义、要求、试验方法、标志、标签、使用说明、包装、运输和贮存。 本标准适用于临床实验室常规检验用的凝血酶时间检测试剂(盒)产品,包括冷冻干燥品和液体试剂产品
Thrombin time reagent(Kit)
本标准规定了凝血酶原时间检测试剂(盒)质量检验测试的通用技术要求,包括术语和定义、要求、试验方法、标志、标签、使用说明、包装、运输和贮存。 本标准适用于临床实验室常规检验用Quick一期法凝血酶原时间检测试剂(盒)产品,包括冷冻干燥品和液体试剂产品。 本标准不适用于床旁快速检测(POCT)的
Prothrombin time reagent(Kit)
本标准规定了活化部分凝血活酶时间检测试剂(盒)质量检验测试的通用技术要求,包括术语和定义、要求、试验方法、标志、标签、使用说明、包装、运输和贮存。 本标准适用于临床实验室常规检验用活化部分凝血活酶时间检测试剂(盒)。 本标准不适用于床旁快速检测(POCT)的活化部分凝血活酶时间检测试剂
Actived partial thromboplastin time reagent(Kit)
Antithrombin Ⅲ testing kit
The document is applicable to the determination of the activated partial thromboplastin time (APTT) in plasma obtained from citrated venous blood
Haemostaseology - Determination of activated partial thromboplastin time (APTT) - Reference measurement procedure
The document is applicable to the determination of the thromboplastin (prothrombin) time (PT) in capillary blood
Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 4: Reference measurement procedure for the determination in capillary blood
Esta norma establece las especificaciones de calidad del jue-go de reactivo para la determinación del tiempo de protrombi-na en sangre
Clinical Methods and Aids Set of Reagents for Determination of Protrombine Time. Quality Specifications
本标准规定了酶联免疫吸附法检测试剂(盒)的通用技术要求,包括术语与定义、分类、要求、试验方法、标识和使用说明书、包装、运输和贮存。 本标准适用于在医学实验室以酶联免疫吸附法为原理进行检验的定量/定性检测试剂(盒)(以下简称“试剂盒
Detection reagent (kit) for enzyme-linked immunoabsorbent assay (ELISA)
1.1 This test method covers the screening of cardiovascular device materials for their ability to induce blood coagulation. This assay should
Standard Test Method for Assessment of Intravascular Medical Device Materials on Partial Thromboplastin Time (PTT)
The purpose of this test method is to determine the time citrated plasma exposed to medical materials takes to form a clot when exposed
Standard Test Method for Assessment of Intravascular Medical Device Materials on Partial Thromboplastin Time (PTT)
The purpose of this test method is to determine the time citrated plasma exposed to medical materials takes to form a clot when exposed
Standard Test Method for Assessment of Intravascular Medical Device Materials on Partial Thromboplastin Time (PTT)
The document is applicable to the determination of the thromboplastin (prothrombin) time (PT) in citrated venous blood
Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 2: Reference measurement procedure for the determination in citrated venous blood
Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 1: Reference measurement procedure for the determination in plasma from citrated venous blood
Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 1: Reference measurement procedure for the determination in plasma from citrated venous blood; Text in German and English
本标准规定了凝血酶时间检测试剂(盒)质量检验测试的通用技术要求,包括术语和定义、要求、试验方法、标志、标签、使用说明、包装、运输和贮存。 本标准适用于临床实验室常规检验用的凝血酶时间检测试剂(盒)产品,包括冷冻干燥品和液体试剂产品
Thrombin time reagent(Kit)
本标准规定了凝血酶原时间检测试剂(盒)质量检验测试的通用技术要求,包括术语和定义、要求、试验方法、标志、标签、使用说明、包装、运输和贮存。 本标准适用于临床实验室常规检验用Quick一期法凝血酶原时间检测试剂(盒)产品,包括冷冻干燥品和液体试剂产品。 本标准不适用于床旁快速检测(POCT)的
Prothrombin time reagent(Kit)
本标准规定了活化部分凝血活酶时间检测试剂(盒)质量检验测试的通用技术要求,包括术语和定义、要求、试验方法、标志、标签、使用说明、包装、运输和贮存。 本标准适用于临床实验室常规检验用活化部分凝血活酶时间检测试剂(盒)。 本标准不适用于床旁快速检测(POCT)的活化部分凝血活酶时间检测试剂
Actived partial thromboplastin time reagent(Kit)
Antithrombin Ⅲ testing kit
The document is applicable to the determination of the activated partial thromboplastin time (APTT) in plasma obtained from citrated venous blood
Haemostaseology - Determination of activated partial thromboplastin time (APTT) - Reference measurement procedure
The document is applicable to the determination of the thromboplastin (prothrombin) time (PT) in capillary blood
Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 4: Reference measurement procedure for the determination in capillary blood
Esta norma establece las especificaciones de calidad del jue-go de reactivo para la determinación del tiempo de protrombi-na en sangre
Clinical Methods and Aids Set of Reagents for Determination of Protrombine Time. Quality Specifications
本标准规定了酶联免疫吸附法检测试剂(盒)的通用技术要求,包括术语与定义、分类、要求、试验方法、标识和使用说明书、包装、运输和贮存。 本标准适用于在医学实验室以酶联免疫吸附法为原理进行检验的定量/定性检测试剂(盒)(以下简称“试剂盒
Detection reagent (kit) for enzyme-linked immunoabsorbent assay (ELISA)
1.1 This test method covers the screening of cardiovascular device materials for their ability to induce blood coagulation. This assay should
Standard Test Method for Assessment of Intravascular Medical Device Materials on Partial Thromboplastin Time (PTT)
The purpose of this test method is to determine the time citrated plasma exposed to medical materials takes to form a clot when exposed
Standard Test Method for Assessment of Intravascular Medical Device Materials on Partial Thromboplastin Time (PTT)
The purpose of this test method is to determine the time citrated plasma exposed to medical materials takes to form a clot when exposed
Standard Test Method for Assessment of Intravascular Medical Device Materials on Partial Thromboplastin Time (PTT)
The document is applicable to the determination of the thromboplastin (prothrombin) time (PT) in citrated venous blood
Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 2: Reference measurement procedure for the determination in citrated venous blood
Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 1: Reference measurement procedure for the determination in plasma from citrated venous blood
Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 1: Reference measurement procedure for the determination in plasma from citrated venous blood; Text in German and English