07.100.10 医学微生物学 标准查询与下载

SN/T 1944-2007 动物及其制品中细菌耐药性的测定 纸片扩散法

本标准规定了动物及其制品中细菌耐药性的纸片扩散检测方法。 本标准适用于动物及其制品中分离的大肠杆菌、沙门氏菌和金黄色葡萄球菌耐药性的检测，其他动物源性细菌的耐药性测定可参考使用本标准。

Detection of antimicrobial resistmceof the bacteria in animal and animal products.Disk diffusion testing

GOST R 52770-2007 医疗产品.安全要求.卫生化学和毒物学试验方法

Medical products. Safety requirements. Methods of sanitation-chemical and toxicological tests

ASTM F2148-06a 用小鼠局部淋巴结分析（LLNA）评价迟发性接触超敏反应的标准实施规程

Standard Practice for Evaluation of Delayed Contact Hypersensitivity Using the Murine Local Lymph Node Assay (LLNA)

ASTM F2148-06 用小鼠局部淋巴结分析（LLNA）评价迟发性接触超敏反应的标准实施规程

Standard Practice for Evaluation of Delayed Contact Hypersensitivity Using the Murine Local Lymph Node Assay (LLNA)

DIN 58943-40:2006 医用微生物学.结核病的诊断.第40部分:分枝杆菌科检测的快速培养规程评价标准

This standard contains evaluation criteria according to which a method may be designated as a procedure for rapid detection of mycobacteria; these criteria permit the comparison of various rapid detection methods as well as the comparison of these types of procedures with the other types of previously standardized methods for the diagnosis of tuberculosis.

Medical microbiology - Diagnosis of tuberculosis - Part 40: Evaluation criteria for fast culture procedures for the detection of mycobacteria

AWWA M48-2006 水上病原体.第2版

The present scope of Committee A21 activity is the development of standards and manuals addressing ductile-iron pressure pipe for water and ductile-iron and gray-iron fittings for use with such pipe. These standards and manuals include topics such as desi

Waterborne Pathogens Second Edition

ASTM E1285-06 噬菌体λ(拉姆达)或它的脱氧核糖核酸的识别标准指南

1.1 This guide covers the procedures for identifying bacteriophage lambda used in biotechnology.1.2 There are hundreds of lambda variants that can be used for biotechnology. These lambda variants are derived from wild type lambda and differ in genome size and genotype.1.3 If the bacteriophage lambda is to be used to construct a recombinant molecule, then the same criteria as prescribed in Section 5 should be used to characterize the newly made DNA.

Standard Guide for Identification of Bacteriophage Lambda (&955;) or Its DNA

DIN 58942-5:2005 医用微生物学.培养基.第5部分:诊断粪便样本用培养基的要求和选取

Medical microbiology - Culture media - Part 5: Requirements and selection of culture media for the diagnostic of stool specimen

ANSI/NSF 49(i9)-2005 II级(层流)生物安全室

Review of standard correcting significant figures between english and metric conversions.

Class II (laminar flow) biosafety cabinetry

DIN 58940-20 Bb.1:2004 医学微生物学.病原细菌对杀菌剂敏感性的测定方法.第20部分:杀菌剂的编码.杀菌剂的代码

Medical microbiology - Susceptibility testing of pathogens to antimicrobial agents - Part 20: Coding of antimicrobial agents - Codes for antimicrobial agents

DIN 58940-4 Bb.1:2004 医学微生物学.病原体对抗菌剂的敏感性试验.第4部分:最小禁用浓度的等级评价.抗菌剂的MIC转效点

Medical microbiology - Susceptibility testing of pathogens to antimicrobial agents - Part 4: Evaluation classes of the minimum inhibitory concentration - MIC-breakpoints of antibacterial agents

NF S92-022*NF EN ISO 18153:2004 体外诊断医疗器材.生物试样的数值测量.校准仪和控制材料赋值的酶催化浓度计量溯源性

In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values for catalytic concentration of enzymes assigned to calibrators and control materials.

DIN 58942-2:2004 医学微生物学.培养基.第2部分:即可使用的血液培养设备

This standard applies to ready-for-use blood culture bottles (BCB), i.e. to blood culture media and their respective containers (blood culture bottles), which are employed for the detection of bacteraemia by means of bacteriological cultures. As they may also be used for detecting septicaemia caused by funghi, information on the detection of funghi is also given in this standard. Ready-for-use blood culture bottles are only suitable for in vitro diagnostics. The purpose of this standard is to specify those physical, chemical and biological requirements for blood culture bottles and blood culture media which are necessary for their diagnostic use. These requirements constitute the prerequisite for ensuring the reliable detection of bacteria in patients' blood.

Medical microbiology - Culture media - Part 2: Ready-to-use blood culture systems

DIN 58967-20:2003 医学微生物学和免疫学.血清学和分子生物学中免疫系统的疾病和传染性疾病的诊断.第20部分:免疫荧光试验(IFT)一般方法的特定要求

The immuno flurescence test is a procedure for the detection of antibodies in the serum. The requirements are valid for the visual interpretation of microscopic methods. The IFT prooves the compound of immunoglobulines on testing antigens. The compound appears by fluorochrome-marked anti-immunoglobulines. The IFT serves for the detection of antibodies and auto-antibodies of various classes and subclasses. The IFT, as described in this standard, represents methodical minimum requirements.

Medical microbiology and immunology - Diagnostics of infectious diseases and diseases of the immune system in serology and molecular biology - Part 20: General method-specific requirements for immunofluorescence tests (IFT)

DIN 58969-10:2003 医用微生物学.血清学和分子生物学中传染性疾病的诊断.第10部分:补体结合试验(CFT)

The complement fixation reaction is a procedure for the diagnosis of infectious diseases. A positiv test result can be the proof of an acute infection or an infection which recently occurred with the corresponding agent. The purpose of these determinations is to render possible comparable test results with the complement fixation reaction from laboratory to laboratory.

Medical microbiology - Diagnostics of infectious diseases in serological and molecular biology - Part 10: Complement fixation test (CFT)

BS EN ISO 17511:2003 体外诊疗装置.生物样品的定量测量.校准仪和控制材料赋值的测量溯源性

ISO 17511:2003 specifies how to assure the metrological traceability of values assigned to calibrators and control materials intended to establish or verify trueness of measurement. The calibrators and control materials are those provided by the manufacturers as part of, or to be used together with, in vitro diagnostic medical devices. External quality assessment (survey) samples, with proven commutability, whose values have been assigned by means of internationally agreed reference measurement systems or internationally agreed conventional reference measurement systems fall within the scope of ISO 17511:2003. ISO 17511:2003 is not applicable to control materials that do not have an assigned value and are used only for assessing the precision of a measurement procedure, either its repeatability or reproducibility (precision control materials); control materials intended for intralaboratory quality control purposes and supplied with intervals of suggested acceptable values, each interval obtained by interlaboratory consensus with respect to one specified measurement procedure, and with limiting values that are not metrologically traceable; correlation between results of two measurement procedures at the same metrological level, purporting to measure the same quantity, because such "horizontal" correlation does not provide metrological traceability; calibration derived from correlation between the results of two measurement procedures at different metrological levels, but with quantities having analytes of different characteristics; metrological traceability of routine results to the product calibrator and their relations to any medical discrimination limit; and properties involving nominal scales, i.e. where no magnitude is involved (e.g. identification of blood cells).

In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values assigned to calibrators and control materials

BS EN ISO 18153:2003 体外诊疗装置.生物样品的定量测量.校准仪和控制系统指定酶的催化浓度的测量溯源性

ISO 18153:2003 specifies how to assure the metrological traceability of values assigned to calibrators and control materials intended to establish or verify trueness of measurement of the catalytic concentration of enzymes. The calibrators and control materials are those provided by the manufacturers as part of, or to be used together with, in vitro diagnostic medical devices. The following subjects are outside the scope of ISO 18153:2003: requirements for the design or selection of a reference measurement procedure; quantities involving mass of enzyme or immunoreactivity of enzymes; control materials that do not have an assigned value and are used only for assessing the precision of a measurement procedure, either its repeatability or reproducibility (precision control materials); control materials intended for intralaboratory quality control purposes and supplied with intervals of suggested acceptable values, each interval obtained by interlaboratory consensus with respect to one specified measurement procedure, and with limiting values that are not metrologically traceable; metrological traceability of routine results to the product calibrator and their relations to any medical discrimination limit; properties involving nominal and ordinal scales.

In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values for catalytic concentration of enzymes assigned to calibrators and control materials

EN ISO 18153:2003 体外诊断医疗设备.生物试样中的数量测量.校准器和控制材料规定的酶催化剂浓度值的测量可追踪性ISO 18153-2003

In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values for catalytic concentration of enzymes assigned to calibrators and control materials ISO 18153:2003

EN ISO 17511:2003 体外诊断医疗设备.生物试样中的数量测量.校准器和控制材料赋予值的测量可追踪性 ISO 17511-2003

In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values assigned to calibrators and control materials ISO 17511:2003

DIN 58942-4:2003 医药微生物学.细菌培养介质.第4部分:细菌标本运输系统

Medical microbiology - Culture media - Part 4: Transport systems for specimens containing bacteria