11.100 实验室医学 标准查询与下载
共找到 753 条与 实验室医学 相关的标准，共 51 页
本标准规定了火焰原子吸收光谱法测定尿中锌浓度的方法 本标准适用于人尿中锌浓度的测定
Urine.Determination of zinc.Flame atomic absorption spectrometric method
- ICS
- 11.100
- CCS
- C05
- 发布
- 1997-01-11
- 实施
- 1997-09-01
本标准规定了石墨炉原子吸收光谱法测定尿中铜浓度的方法。 本标准适用于职业接触人群尿中铜浓度的检测。
Urine.Determination of copper.Graphite furnace atomic absorption spectrometry method
- ICS
- 11.100
- CCS
- C05
- 发布
- 1997-01-11
- 实施
- 1997-09-01
本标准规定了反相高效液相色谱测定尿中肌酐浓度的方法。 本标准适用于人尿中肌酐浓度的测定。
Urine.Determination of creatinine.Reversed-phase high performance liquid chromatographic method
- ICS
- 11.100
- CCS
- C05
- 发布
- 1997-01-11
- 实施
- 19970901
本标准规定了用离子选择电极法测定尿中无机氟化物含量的测定方法。 本标准适用于测定人群或动物尿中无机氟化物含量。
Determination of fluorine in urine.Ion selective electrode method
- ICS
- 11.100
- CCS
- C05
- 发布
- 1997-01-11
- 实施
- 1997-09-01
本标准规定了顶空气相色谱法测定尿中三氯乙酸浓度的方法。 本标准适用于接触三氯乙烯的工人尿中三氯乙酸浓度的测定。
Urine.Determination of trichloroacetic acid.Headspace gas chromatographic method
- ICS
- 11.100
- CCS
- C05
- 发布
- 1997-01-11
- 实施
- 19970901
Standard Practice for Assessment of Hemolysis in Continuous Flow Blood Pumps
- ICS
- 11.100
- CCS
- 发布
- 1997-01-01
- 实施
Standard Practice for Selection of Blood for In Vitro Evaluation of Blood Pumps
- ICS
- 11.100
- CCS
- 发布
- 1997-01-01
- 实施
1.1 This specification covers requirements for glass reusable blood diluting pipets that are used for performing red and white cell corpuscle determinations.
Standard Specification for Pipet, Blood Diluting
- ICS
- 11.100
- CCS
- 发布
- 1997
- 实施
1.1 This specification describes requirements for a tube that measures the erythrocyte sedimentation rate (ESR). ESR is the suspension stability of red cells in diluted, anti-coagulated human blood. 1.1.1 The use of the term “rate” is, strictly speaking, not correct. The test measures the amount of settling of red cells after a specified time. 1.2 The tubes are used together with a special rack to ensure they remain in a vertical position during the test. 1.3 This specification includes many dimensional requirements that are, for the most part, in agreement with the British Standards Institution, German Standards Institute, International Committee for Standardization in Haematology, and the National Committee for Clinical Laboratory Standards publications on Westergren tubes. The clinical procedure using the tube described in this specification is known as the “Westergren Method.” 1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard. 1.5 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.
Standard Specification for Glass Westergren Tube, Reusable
- ICS
- 11.100
- CCS
- 发布
- 1997
- 实施
The objective of this practice is to standardize the evaluation method for detecting the hemolytic effect of a continuous flow blood pump used in extracorporeal circulation and circulatory assistance. 1.1 This recommended practice covers a protocol for the assessment of the hemolytic properties of continuous flow blood pumps used in extracorporeal or implantable circulatory assist. An assessment is made based on the pump''s effects on the erythrocytes over a certain period of time. For this assessment, a recirculation test is performed with a pump for 6h. 1.2 The values stated in both inch-pound and SI units are to be regarded as the standard. The SI units given in parentheses are for information only. 1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.
Standard Practice for Assessment of Hemolysis in Continuous Flow Blood Pumps
- ICS
- 11.100
- CCS
- C30
- 发布
- 1997
- 实施
6.1 The objective of this practice is to standardize the evaluation method for detecting the hemolytic effect of a continuous flow blood pump used in extracorporeal circulation and circulatory assistance. 1.1 This practice covers a protocol for the assessment of the hemolytic properties of continuous flow blood pumps used in extracorporeal or implantable circulatory assist. An assessment is made based on the pump's effects on the erythrocytes over a certain period of time. For this assessment, a recirculation test is performed with a pump for 6 h. 1.2 The values stated in either SI units or inch-pound units are to be regarded separately as standard. The values stated in each system may not be exact equivalents; therefore, each system shall be used independently of the other. Combining values from the two systems may result in non-conformance with the standard. 1.3 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.
Standard Practice for Assessment of Hemolysis in Continuous Flow Blood Pumps
- ICS
- 11.100
- CCS
- 发布
- 1997
- 实施
This document presents reference methods for determination of minimum inhibitory concentrations (MIC) of aerobic bacteria by broth macrodilution, broth microdilution, and agar dilution, including updated interpretive and quality control tables.
Methods for Dilution Antimicrobial Susceptibility Tests for Bacteria that Grow Aerobically
- ICS
- 11.100
- CCS
- C44
- 发布
- 1997
- 实施
This document presents current recommended techniques for disk susceptibility testing, criteria for quality control testing, and updated tables for interpretive zone diameters.
Performance Standards for Antimicrobial Disk Susceptibility Tests
- ICS
- 11.100
- CCS
- C44
- 发布
- 1997
- 实施
5.1 The test results are substantially affected by donor species and age, the method of harvesting, the period of storage, the biochemical state of the blood, and the hemoglobin and hematocrit level of blood.3,4 Therefore, standardization of proper blood usage for in vitro evaluation of blood pumps is essential, and this recommended practice will allow a universal comparison of test results. 5.2 Drawing several units of blood from healthy cattle does not affect them or their health. Therefore, bovine blood is strongly suggested for usage in experimental evaluation of blood damage. Mixing two donor sources of blood should be avoided in hemolysis tests because the mixture may induce added hemolysis or a change in red cell resistance against trauma. 1.1 This practice covers blood that will be used for in vitro performance assessments of blood pumps. These assessments include the hemolytic properties of the devices. 1.2 This practice covers the utilization of blood for the in vitro evaluation of the following devices: 1.2.1 Continuous flow rotary blood pumps (roller pumps, centrifugal pumps, axial flow pumps, and so forth) (see Practice F1841). 1.2.2 Pulsatile blood pumps (pneumatically driven, electromechanically driven, and so forth). 1.3 The source of blood utilized for in vitro evaluation of blood trauma (that is, hemolysis caused by the blood pumps, due to the pump design, construction, and materials used) substantially influences the results of the performance of these devices. Thus, a standardized blood source is required. 1.4 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
Standard Practice for Selection of Blood for
- ICS
- 11.100
- CCS
- 发布
- 1997
- 实施
本标准规定了尿中砷的氢化物发生火焰原子吸收光谱测定方法。 本法最低检测浓度为0.002 mg/L。 本标准适用于正常人和接触砷作业工人尿中砷的测定。
Urine.Determination of arsenic.Hydride generation-flame atomic absorption spectrometry
- ICS
- 11.100
- CCS
- C05
- 发布
- 1996-10-14
- 实施
- 1997-05-01
本标准规定了尿中氟的离子选择电极测定方法。 本法最低检测浓度为0.1 mg/L。 本标准适用于正常人和接触无机氟工人尿中氟的测定。
Urine.Determination of fluoride.Ion specifi electrode method
- ICS
- 11.100
- CCS
- C05
- 发布
- 1996-10-14
- 实施
- 1997-05-01
本标准规定了尿中镉的火焰原子吸收光谱测定方法。 本法最低检测浓度为0.22 μg/L。 本标准适用于正常人和接触镉的工人尿中镉的测定。
Urine.Determination of cadmium.Flame atomic absorption spectrometric method
- ICS
- 11.100
- CCS
- C05
- 发布
- 1996-10-14
- 实施
- 1997-05-01
本标准规定了尿中镉的石墨炉原子吸收光谱测定方法。 本法最低检测浓度为0.28 μg/L。 本标准适用于正常人和接触镉的工人尿中镉的测定。
Urine.Determination of cadmium.Graphite furnace atomic absorption spectrometric method
- ICS
- 11.100
- CCS
- C05
- 发布
- 1996-10-14
- 实施
- 1997-05-01
本标准规定了尿中镉的微分电位溶出测定方法。 本法最低检测浓度为0.2 μg/L。 本标准适用于正常人和接触镉人员尿中镉的测定。
Urine.Determination of cadmium.Differential potentiometric stripping method
- ICS
- 11.100
- CCS
- C05
- 发布
- 1996-10-14
- 实施
- 1997-05-01
本标准规定了血中镉的石墨炉原子吸收光谱测定方法。 本法最低检测浓度为0.66 μg/L。 本标准适用于正常人和接触镉的工人血中镉的测定。
Blood.Determination of cadmium.Graphite furnace atomic absorption spectrometric method
- ICS
- 11.100
- CCS
- C05
- 发布
- 1996-10-14
- 实施
- 1997-05-01
