07.100.10 医学微生物学 标准查询与下载

DIN 58959-14:1997 医疗微生物学质量管理.第14部分:需氧菌敏感性检验对照菌株要求

The document refer to the conditions and methods that shall be followed for the use of control strains during susceptibility testing of aerobic, fast-growing bacteria according to which the results obtained with the control strains are to be evaluated.#,,#

Quality management in medical microbiology - Part 14: Requirements for the use of control strains for susceptibility testing of aerobic bacteria

DIN 58959-13:1997 医用微生物学质量管理.第13部分:灵敏度检验对照菌株用有效物料极限值测定准则

The document is valid for the determination of the active substance control limits of control used for the susceptibility testing of pathogens against chemotherapeutics for surveillance and control of the test methods used.

Quality management in medical microbiology - Part 13: Criteria for determination of active substance breakpoint for control strains used in susceptibility testing

DIN 58959-1:1997 医疗微生物学质量管理.第1部分:质量管理(QM)体系要求

Quality management in medical microbiology - Part 1: Requirements for the QM system

DIN 58959-4:1997 医疗微生物学质量管理.第4部分:光学显微镜测试要求

The document is valid for light-microscope investigations according to clause 4.1 which are carried out in medical-microbiological laboratories according to DIN 58956-1 for the portrayal, recognition and identification of microorganisms originating from natural or pre-treated specimens or from cultures of microorganisms. The aim of this standard is the assurance of the quality investigations by optical (light) microscopy by the establishment of minimum requirements for the work-station, the technical equipment and methods used.

Quality management in medical microbiology - Part 4: Requirements for investigations using light microscopes

DIN 58959-3:1997 医疗微生物学质量管理.第3部分:申请表和报告单要求

The document applies to all request for investigation of specimens sent to medical microbiological laboratories according to DIN 58956-1 and reports which are made out to these laboratories to communicate the results of investigations related to patients.

Quality management in medical microbiology - Part 3: Requirements for request and report forms

ASTM E1280-97(2008) 哺乳动物细胞诱变性用老鼠淋巴瘤鉴定实施的标准指南

This guide is limited to procedures used solely for the testing of substances to determine their mutagenicity and does not apply to other methods and uses such as exploring mechanisms of mutation. Recent evidence suggests that this assay measures a dual genetic end point; therefore, some discussion of the relationships between mammalian cell mutagenicity testing results and the results observed both in pure gene mutational assays and in cytogenetic assays is necessary. However, it is not the intent of this guide to discuss other relationships between this mammalian cell mutagenicity testing results and the results observed in other tests for mutagenicity and carcinogenicity.1.1 The purpose and scope of this guide is to present background material and to establish criteria by which protocols and procedures for conducting the L5178Y/TK+/−-3.7.2C mouse lymphoma mutagenicity assay (commonly referred to as the mouse lymphoma assay, (MLA)) can be properly understood and evaluated. This guide is also intended to aid researchers and others to gain a better understanding of the critical elements involved with mammalian cell mutagenicity testing. More specifically, this guide is intended to provide for researchers the accomplishment of the following goals: 1.1.1 Provide an understanding of the critical procedures (steps) in the performance of this mammalian cell mutagenicity test. 1.1.2 Provide generalized criteria by which researchers can evaluate if they are properly performing, utilizing, and interpreting this assay. 1.1.3 Provide criteria by which individuals responsible for evaluating MLA data can determine if the experiments have been properly performed and interpreted. 1.1.4 Provide a basis from which new procedures and developments in testing procedures can be evaluated. 1.1.5 Provide an understanding of the types of genetic damage (that is, gene and chromosome mutation) that may be detected in this mammalian cell mutagenicity test. 1.2 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.

Standard Guide for Performing the Mouse Lymphoma Assay for Mammalian Cell Mutagenicity

DIN 58943-3:1996 医用微生物学.结核诊断.第3部分:真菌验证培养法

Medical microbiology - Diagnosis of tuberculosis - Part 3: Detection of mycobacteria by culture methods

DIN 58943-8:1996 医用微生物学.结核病诊断.第8部分:结核菌对化疗药剂敏感性的测定方法

This document is valid for the susceptibility testing of tubercle bacilli of the species mycobacterium tuberculosis including its geographical variants, mycobacterium bovis and BCG stains against chemotherapeutic agents. The method described in this document is considered a reference method against which other routine methods, as e.g. the radiomeric examination in Middlebrook medium, shall be assessed.#,,#

Medical microbiology - Diagnosis of tuberculosis - Part 8: Methods for the determination of susceptibility of tubercle bacilli to chemotherapeutic agents

ASTM D5952-96(2002) 军团病（军团病或庞蒂亚克热）水系统检查和可能爆发的军团病调查的标准指南

Standard Guide for Inspecting Water Systems for Legionellae and Investigating Possible Outbreaks of Legionellosis (Legionnaires' Disease or Pontiac Fever)

DIN 58962-3:1996 医疗微生物学.下呼吸道感染诊断.第3部分:细菌和真菌培养化验

This document applies to cultural examination methods for the detection and differentiation of pathogenic as well as facultatively pathogenic bacteria (excluding mycobacteria) and fungi edemically present in Europe from specimens taken from the lower respiratory tract under consideration of the natural flora of the respiratory tract's mucous membrane.

Medical microbiology - Diagnosis of infections of the lower respiratory tract - Part 3: Cultural examination for the detection of bacteria and fungi

DIN 58943-7:1995 医用微生物学.肺结核诊断.第7部分:勒温-杰森分枝杆菌生长的更改介质

The document specifies a modified L攚enstein-Jensen culture medium which is used for the growth of mycobacteria according to DIN 58943-3 as well as for susceptibility testing of tubercle bacteria according to DIN 58943-8. Its purpose is to fix the biological minimum requirements by defining its composition, production and quality testing.#,,#

Medical microbiology - Diagnosis of tuberculosis - Part 7: Modified Loewenstein-Jensen medium for the growth of mycobacteria

DIN 58942-5 Bb.1:1995 医用微生物学.细菌培养介质.第5部分:粪便试样诊断用培养介质的要求和选择、常规检验用粪便的逐步检验和介质培养测定的原则

Medical microbiology - Culture media for use in bacteriology - Part 5: Requirements and selection of cultur media for the diagnostics of stool specimens, diagnostics of stool specimens, principles of step-by-step examination of stool and survey of culture

DIN 58943-32:1995 医用微生物学.肺结核诊断.第32部分:检测分枝杆菌的显微镜法

Medical microbiology - Diagnosis of tuberculosis - Part 32: Detection of mycobacteria by microscopic methods

DIN 58962-2:1994 医疗微生物学.下呼吸道感染诊断.第2部分:显微诊察

The document applies to the microscopic examination of specimen according to DIN 58962-1 for the detection of cells or microorganisms for the diagnosis of infections of the lower respiratory tract.

Medical microbiology - Diagnosis of infections of the lower respiratory tract (LRT) - Part 2: Microscopic examination

DIN 58962-1:1994 医疗微生物学.下呼吸道感染诊断.第1部分:术语、一般要求

The document describes microbiological and immunological test methods for the diagnosis of infectious diseases of the lower respiratory tract. It specifies minimum requirements for the detection of bacteria, funghi endemic to Europe, and pneumocystis carinii via mikroskopic, cultural, and immunological methods.

Medical microbiology - Diagnosis of infections of the lower respiratory tract (LRT) - Part 1: Terminology, general requirements

DIN 58940-7:1994 医用微生物学.病原体(分枝杆菌除外)对抗菌剂敏感性的测定方法.第7部分:用微稀释法对最小细菌浓度的测定

Medical microbiology - Methods for the determination of susceptibility of pathogens (except mycrobacteria) to antimicrobial agents - Part 7: Determination of the minimum bactericidal concentration (MBC) with the aid of microdilution

DIN 58969-41:1994 医用微生物学.传染病的血清诊断.免疫缺陷斑(IB).第41部分:防止人体免疫缺乏病毒 HIV-1 或 HIV-2 抗体的检测用特殊要求

The document is valid for the detection of antibodies against HIV-1 or HIV-2 in serum, plasma or other body liquids via Immunoblot (IB) according by DIN 58967-40.#,,#

Medical microbiology; serodiagnosis of infectious diseases; immunoblot (IB); part 41: special requirements for the detection of antibodies against Human Immunodeficiency Virus HIV-1 or HIV-2

DIN 58943-9:1993 医用微生物学.结核病的诊断.鉴别结核杆菌的最低要求

This document applies for the identification of tubercle bacilli (in the anglo-saxon writing called: Tb-complexe). Its aim is, to lay down the examinations necessary to identify the various kinds of tubercle bacilli and to lay down a reference method for each of these examinations, to ensure a comparability of results. For identification of other mycobacterial kinds, the examinations mentioned in this document will not be enough.#,,#

Medical microbiology; diagnosis of tuberculosis; minimum requirements for the identification of tubercle bacilli

ASTM E1535-93(2006) 厌氧消化系统性能评定的标准试验方法

This test method will yield data that will form a performance profile for an anaerobic digester facility. The significance of this profile is that it can be compared directly to another facilityrsquo; performance profile and yield a measurement of expected facility performance under field conditions. This test method will also yield data that can be used to verify the operation of a system to a regulatory agency. The single black box technique applied to performance evaluation examines only the overall input/output relationship. This implies that the operation of the facility during the tests will be conducted to achieve design conditions in accordance with established procedures.1.1 This test method is applicable to all anaerobic digestion systems.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 Test Method for Performance Evaluation of Anaerobic Digestion Systems

YY 0027-1990 电热恒温培养箱

本标准规定了电热恒温培养箱的术语、产品分类、技术要求、试验方法、检验规则和标志、包装，运输及贮存等要求。 本标准适用于0.5m^(3)以下的电热恒温培养箱，该产品系细菌培养、育种、发酵及温度不高于60℃的其他恒温试验的设备。

Electric heated incubators of constant temperature