歡迎訪問中科光析科學技術(shù)研究所官網(wǎng)!
免費咨詢熱線
400-635-0567
計數(shù)用培養(yǎng)基檢測項目報價???解決方案???檢測周期???樣品要求? |
點 擊 解 答??![]() |
本標準規(guī)定了食品微生物學檢驗用培養(yǎng)基和試劑的質(zhì)量要求。本標準適用于食品微生物學檢驗用培養(yǎng)基和試劑的質(zhì)量控制。
本標準規(guī)定了紙和紙板內(nèi)部及表面菌落總數(shù)的測定方法。本標準適用于大多數(shù)紙和紙板,尤其是與食品接觸的紙和紙板。
GB/T l2763的本部分規(guī)定了海洋生物調(diào)查的一般規(guī)定、技術(shù)要求和調(diào)查(測定)要素、采樣、樣品分析及資料整理的基本要求和方法。 本部分適用于海洋環(huán)境基本要素調(diào)查中的海洋生物調(diào)查。
適用GB 18281的本部分規(guī)定了擬用于確認和監(jiān)測滅菌周期的生物指示物(包括染菌載體、試驗菌懸液)及其他組成部分在生產(chǎn)、標識、檢測方法和性能方面的通用要求。本部分的基本要求適用于GB 18281的其他各部分。對于用于特殊滅菌過程中的生物指示物的要求在GB 18281的其他部分都有所規(guī)定。本部分適用于沒有特殊要求的生物指示物。不適用本部分不適用于依靠物理方式去除微生物的檢測體系,例如過濾過程或利用清洗消毒器或流通蒸汽等物理和/或機械方法去除微生物的過程。然而,本部分應(yīng)包含相應(yīng)的微生物測試系統(tǒng)的內(nèi)容。
本標準規(guī)定了化妝品中需氧嗜溫性細菌的常規(guī)檢測和計數(shù)方法,可經(jīng)需氧培養(yǎng)后對瓊脂培養(yǎng)基上的菌落數(shù)計數(shù),或檢查經(jīng)增菌后有無細菌生長。本標準可能不適用于某些難溶于水的產(chǎn)品和清潔類用品等樣品的檢驗,可用被證實具有相同效果其他試驗方法替代。必要時,可選用本標準的參考文獻中列舉的確證方法對檢測和計數(shù)的微生物進行確證。
本標準規(guī)定了醫(yī)用透明質(zhì)酸鈉凝膠的分類、要求、檢驗規(guī)則、標志和包裝。本標準適用于醫(yī)用透明質(zhì)酸鈉凝膠。醫(yī)用透明質(zhì)酸鈉凝膠適用范圍包括眼科手術(shù)的黏彈劑、關(guān)節(jié)腔內(nèi)注射的潤滑劑和外科手術(shù)的阻隔劑。
本標準規(guī)定了麻醉和呼吸設(shè)備及組成應(yīng)用與氧氣所接觸的材料,在氣體壓力大于50 kPa的正?;騿我还收蠣顟B(tài)下與氧氣兼容性的低要求。本標準適用于麻醉和呼吸設(shè)備,例如:醫(yī)用氣體管道系統(tǒng)、減壓器、終端、醫(yī)用供應(yīng)單元、撓性連接、流量計裝置、麻醉工作站和呼吸機。本標準提出的兼容性特征包括:清潔度、阻燃性、燃燒和/或分解產(chǎn)物的毒性。
本標準規(guī)定了用于外科植入物和組織工程醫(yī)療器械產(chǎn)品透明質(zhì)酸鈉的要求、試驗方法等。本標準適用于制備組織工程醫(yī)療器械產(chǎn)品及其支架材料的透明質(zhì)酸鈉。
本標準規(guī)定了竹漿粘膠長絲、竹漿連續(xù)紡粘膠長絲的產(chǎn)品標識、要求、試驗方法、檢驗規(guī)則、包裝、標志和運輸?shù)?。本標準適用于以竹漿粕為原料,以半連續(xù)紡或連續(xù)紡工藝生產(chǎn)的竹漿粘膠長絲。其密度在55.5dtex-333.3dtex范圍,單絲線密度為2dtex-7dtex。其他類型的粘膠長絲可以參照使用。
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\".