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计数用培养基检测项目报价? 解决方案? 检测周期? 样品要求? |
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本标准规定了食品微生物学检验用培养基和试剂的质量要求。本标准适用于食品微生物学检验用培养基和试剂的质量控制。
本标准规定了纸和纸板内部及表面菌落总数的测定方法。本标准适用于大多数纸和纸板,尤其是与食品接触的纸和纸板。
GB/T l2763的本部分规定了海洋生物调查的一般规定、技术要求和调查(测定)要素、采样、样品分析及资料整理的基本要求和方法。 本部分适用于海洋环境基本要素调查中的海洋生物调查。
适用GB 18281的本部分规定了拟用于确认和监测灭菌周期的生物指示物(包括染菌载体、试验菌悬液)及其他组成部分在生产、标识、检测方法和性能方面的通用要求。本部分的基本要求适用于GB 18281的其他各部分。对于用于特殊灭菌过程中的生物指示物的要求在GB 18281的其他部分都有所规定。本部分适用于没有特殊要求的生物指示物。不适用本部分不适用于依靠物理方式去除微生物的检测体系,例如过滤过程或利用清洗消毒器或流通蒸汽等物理和/或机械方法去除微生物的过程。然而,本部分应包含相应的微生物测试系统的内容。
本标准规定了化妆品中需氧嗜温性细菌的常规检测和计数方法,可经需氧培养后对琼脂培养基上的菌落数计数,或检查经增菌后有无细菌生长。本标准可能不适用于某些难溶于水的产品和清洁类用品等样品的检验,可用被证实具有相同效果其他试验方法替代。必要时,可选用本标准的参考文献中列举的确证方法对检测和计数的微生物进行确证。
本标准规定了医用透明质酸钠凝胶的分类、要求、检验规则、标志和包装。本标准适用于医用透明质酸钠凝胶。医用透明质酸钠凝胶适用范围包括眼科手术的黏弹剂、关节腔内注射的润滑剂和外科手术的阻隔剂。
本标准规定了麻醉和呼吸设备及组成应用与氧气所接触的材料,在气体压力大于50 kPa的正常或单一故障状态下与氧气兼容性的低要求。本标准适用于麻醉和呼吸设备,例如:医用气体管道系统、减压器、终端、医用供应单元、挠性连接、流量计装置、麻醉工作站和呼吸机。本标准提出的兼容性特征包括:清洁度、阻燃性、燃烧和/或分解产物的毒性。
本标准规定了用于外科植入物和组织工程医疗器械产品透明质酸钠的要求、试验方法等。本标准适用于制备组织工程医疗器械产品及其支架材料的透明质酸钠。
本标准规定了竹浆粘胶长丝、竹浆连续纺粘胶长丝的产品标识、要求、试验方法、检验规则、包装、标志和运输等。本标准适用于以竹浆粕为原料,以半连续纺或连续纺工艺生产的竹浆粘胶长丝。其密度在55.5dtex-333.3dtex范围,单丝线密度为2dtex-7dtex。其他类型的粘胶长丝可以参照使用。
This European Standard specifies a test method and the minimum requirements for bactericidal activity of chemical disinfectant and antiseptic products that form a homogeneous, physically stable preparation when diluted with hard water or-in the case of ready-to-use products-with water. Products can only be tested at a concentration of 80 % or less, as some dilution is always produced by adding the test organisms and interfering substance.This European Standard applies to products that are used in the veterinary area-e. g. in the breeding, husbandry, transport and disposal of all animals except when in the food chain following death and entry to the processing industry. EN 14885 specifies in detail the relationship of the various tests to one another and to \"use recommendations\". NOTE 1 The method described is intended to determine the activity of commercial formulations or active substances under the conditions in which they are used. NOTE 2This method corresponds to a phase 2 step 1 test.
The document specifies a test method and requirements for minimum bactericidal activity of chemical disinfectant and antiseptic products that form a homogenous physically stable preparation in water. The document is applicable to products for use in agricultural (but not crop protection), domestic service, food hygiene and other industrial fields, institutional, medical and veterinary applications.
This standard gives general instructions for carrying out microbiological examinations in accordance with specific standards. To help to ensure the validity of the examinations. To ascertain the general techniques used for conducting the examinations are the same in all labs. To help to achieve homogeneous results.
This European Standard specifies a test method and the minimum requirements for basic bactericidal activity of chemical disinfectant and antiseptic products that form a homogeneous, physically stable preparation when diluted with water. Products can only be tested at a concentration of 80 % or less as some dilution is always produced by adding the test organisms and water.This European Standard applies to active substances (antibacterial biocides) and to formulations under development that are planned to be used in food, industrial, domestic and institutional, medical and veterinary areas. It applies also to the evaluation of bactericidal activity of chemical antiseptics and disinfectants whenappropriate standards are not available.NOTE 1 This European Standard does not evaluate the activity of a product for an intended use.NOTE 2 This method corresponds to a phase 1 test (Annex F).
This document specifies a test method and the minimum requirements for mycobactericidal (or tuberculocidal) activity of chemical disinfectant products that form a homogeneous, physically stable preparation when diluted with hard water - or in the case of ready-to-use products - with water. Products can only be tested at a concentration of 80 % or less as some dilution is always produced by adding the test organisms and interfering substance.\nThis document applies to products that are used in the medical area including those that are covered by the EEC/93/42 Directive on Medical Devices.\nThis document applies to areas and situations where disinfection is medically indicated. Such indications occur in patient care, for example:\nin hospitals, in community medical facilities and in dental institutions; \nin clinics of schools, of kindergartens and of nursing homes;\nand may occur in the workplace and in the home. It may also include services such as laundries and kitchens supplying products directly for the patients.\nNOTE 1 The method described is intended to determine the activity of commercial formulations or active substances under the conditions in which they are used.\nNOTE 2 This method corresponds to a phase 2, step 1 test (see Annex E).
This European Standard specifies a test method and the minimum requirements for bactericidal activity ofchemical disinfectant products that form a homogeneous, physically stable preparation when diluted with hardwater – or in the case of ready-to-use products – with water.This European Standard applies to products that are used in the medical area for disinfecting instruments byimmersion – even if they are not covered by the EEC/93/42 Directive on Medical Devices.This European Standard applies to areas and situations where disinfection is medically indicated. Suchindications occur in patient care, for example: in hospitals, in community medical facilities and in dental institutions; in clinics of schools, of kindergardens and of nursing homes; and may occur in the workplace and in the home. It may also include services such as laundries andkitchens supplying products directly for the patients.NOTE This method corresponds to a phase 2, step 2 test (see Annex E).
This European Standard specifies a test method and the minimum requirements for fungicidal or yeasticidalactivity of chemical disinfectant products for instruments that form a homogeneous, physically stablepreparation when diluted with hard water – or in the case of ready-to-use products – with water.This European Standard applies to products that are used in the medical area for disinfecting instruments byimmersion – even if they are not covered by the EEC/93/42 Directive on Medical Devices.This European Standard applies to areas and situations where disinfection is medically indicated. Suchindications occur in patient care, for example: in hospitals, in community medical facilities and in dental institutions; in clinics of schools, of kindergardens and of nursing homes;and may occur in the workplace and in the home. It may also include services such as laundries and kitchenssupplying products directly for the patients.NOTE This method corresponds to a phase 2, step 2 test (see Annex E).
This European Standard specifies a test method and the minimum requirements for mycobactericidal ortuberculocidal activity of chemical disinfectant products that form a homogeneous, physically stablepreparation when diluted with hard water, or – in the case of ready-to-use products – with water.This European Standard applies to products that are used in the medical area for disinfecting instruments byimmersion – even if they are not covered by the EEC/93/42 Directive on Medical Devices.This European Standard applies to areas and situations where disinfection is medically indicated. Suchindications occur in patient care, for example: in hospitals, in community medical facilities and in dental institutions; in clinics of schools, kindergartens and nursing homes;and may occur in the workplace and in the home. It may also include services such as laundries and kitchenssupplying products directly for the patients.EN 14885 specifies in detail the relationship of the various tests to one another and to \"use recommendations\".