檢測項目(部分)
氣味
穩(wěn)定性
鎘
外觀
pH
甲醛
耐熱大腸菌群
耐熱
菌落總數(shù)
耐寒
凈含量
全部參數(shù)
鉛
砷
金黃色葡萄球菌
甲醇
二噁烷
抑菌率
銅綠假單胞菌
甲醛含量
總有效物
檢測樣品(部分)
洗手液
特種洗手液
檢測標(biāo)準(zhǔn)(部分)
本部分適用于主要以表面活性劑和調(diào)理劑配置而成的,具有清潔及抗菌、抑菌特種功能的洗手液產(chǎn)品(不適用于非水洗型產(chǎn)品)。
本標(biāo)準(zhǔn)適用于以表面活性劑為有效成分配制的用于手部清潔的產(chǎn)品。
本標(biāo)準(zhǔn)不適用于非水洗型產(chǎn)品。
The procedure may be used to test the effectiveness of antimicrobial handwashing agents. The test formulations may be designed for frequent use to reduce the transient bacterial flora on hands.
1.1 This test method covers the determination of the effectiveness of antimicrobial handwashing agents for the reduction of transient microbial flora when used in a handwashing procedure.
1.2 A knowledge of microbiological techniques is required for these procedures.
1.3 In this test method metric units are used for all applications except for distance in which case inches are used and metric units follow in parentheses.
1.4 This test method may be used to evaluate topical antimicrobial handwash formulations.
1.5 Performance of this procedure requires the knowledge of regulations pertaining to the protection of human subjects.
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.
1.1 This test method is designed to determine the effectiveness of antimicrobial handwashing agents for the reduction of transient microbial flora when used in a handwashing procedure.
1.2 A knowledge of microbiological techniques is required for these procedures.
1.3 In this test method metric units are used for all applications except for distance in which case inches are used and metric units follow in parentheses.
1.4 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. For more specific precautionary statements see Note 1.
1.4 This method may be used to evaluate topical antimicrobial handwash formulations.
1.5 Performance of this procedure requires the knowledge of regulations pertaining to the protection of human subjects.
1.1 This test method covers determining the effectiveness of an antibacterial handwash for reducing the level of aerobic bacterial flora on the hands following an extended period of use.
1.2 A knowledge of microbiological techniques is required for these procedures.
1.3 In this test method metric units are used for all applications except for distance. In this case inches are used and metric units follow in parentheses.
1.4 Performance of this procedure requires the knowledge of regulations pertaining to the protection of human subjects. (Title 21 CFR Part 50).
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.
This in vivo procedure is designed to test the ability of hygienic handwash or handrub agents to eliminate fungal contamination from experimentally-contaminated hands. Since the two thumbpads and all eight fingerpads can be used in any given test it allows for the incorporation of an input control (two) control for viable cells of the test fungus remaining after the inoculum has been allowed to dry (two) fungal cells eliminated after treatment with a control or reference solution (two) and up to four replicates to assess the fungus-eliminating efficiency of the formulation under test. No more than 100 x00B5;L of the test fungal suspension is required to complete one test.
Whereas this test method is designed to work with fungi
similar ASTM standards exist for testing against viruses (Test Method E 1838
Infectious microorganisms left on hands after washing can be reduced further by drying the washed hands with paper cloth or warm air (5). A step for the drying of fingerpads after exposure to the control or test solution therefore has not been included to avoid fungal removal by the drying process itself.
This test method is not meant for testing surgical hand scrubs or preoperative skin preps.
The level of contamination with viable fungi on each fingerpad after the drying of the inoculum should be at least 104 CFU so that it would permit the detection of up to a 4-log10 reduction in the viability titer of the test organism by a test formulation under the conditions of this test. This in itself does not represent the product performance criterion which may vary depending on the jurisdiction and the nature of the formulation being evaluated.
1.1 This test method is designed to assess the ability of hygienic handwash and handrub agents to reduce levels of fungal contamination on hands (3). This test method is not meant for use with surgical hand scrubs (Test Method E 1115
1.2 Performance of this procedure requires the knowledge of regulations pertaining to human experimentation.
1.3 The test method should be performed by persons with training in microbiology in facilities designed and equipped for work with infectious agents at biosafety level 2 (4).
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.
This procedure has been designed to evaluate handwash products using a palmar surface only contamination method. This method is an alternative contamination procedure to that listed in Test Method E1174. The current contamination procedure in Test Method E1174 describes a standardized procedure for contaminating the entire hand palmar surface and back directly using a marker organism. The contamination procedure in Test Method E1174 does not necessarily represent real world hand contamination. During routine activities it is only the palmar surface comprising palms fingers and finger pads of the hands that becomes contaminated by contact with transient microorganisms. These microorganisms can then be transferred to food or objects. Methods to measure the amount of microorganisms transferred to food or objects can be found in Fischler et al and Fuls et al and will be developed into a future ASTM standard.
1.1 This test method covers the determination of the effectiveness of antimicrobial handwashing agents for the reduction of transient microbial flora when used in a handwashing procedure.
1.2 A knowledge of microbiological techniques is required for these procedures.
1.3 This test method may be used to evaluate topical antimicrobial handwash formulations.
1.4 Performance of this procedure requires the knowledge of regulations pertaining to the protection of human subjects.
1.5 In this test method SI units are used for all applications except for distance in which case inches are used and SI units follow in parentheses.
1.6 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. For more specific precautionary statements see 8.5.
1.1 This practice covers and is designed to determine the relative effectiveness of antimicrobial handwashing agents in reducing transient microorganisms using a controlled handwash.
1.2 Knowledge of microbiological techniques is required for these procedures.
1.3 This practice is used to evaluate topical antimicrobial handwashing formulations.
1.4 Performance of this procedure requires the knowledge of regulations pertaining to the protection of human subjects (21 CFR Parts 50 and 56).
1.5 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.6 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 health and environmental practices and determine the applicability of regulatory limitations prior to use. For more specific precautionary statements see 8.1.
1.7 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the D
This in vivo procedure is designed to test the ability of hygienic handwash and handrub agents to reduce levels of selected infectious viruses from experimentally contaminated fingerpads of adults. Since the two thumbpads and all eight fingerpads can be used in any given test it allows for the incorporation of input virus control (two) virus remaining viable after the inoculum has been allowed to dry (two) virus eliminated after treatment with a control or reference solution (two) and up to four replicates to assess the virus-eliminating efficiency of the substance under test. No more than 100 x03BC;L of the virus suspension are required to complete one test. The results of testing with this test method may form the basis for further tests using a suitable whole-hand test protocol (for example Test Method E2011).
This test method is designed to be performed by a trained individual who is responsible for choosing the appropriate host system for the test virus and applying the techniques necessary for propagation and maintenance of host and test virus. For a reference text refer to Lennette et al (8).
Whereas the method described here relates to testing with viruses of human origin it can be readily adapted to work with animal pathogenic viruses as well as bacteriophages. Standard methods for working with bacteria (Test Method E2276) and fungi (Test Method E2613) are also available.
Infectious microorganisms left on hands after washing can be reduced further by drying the washed hands with paper cloth or warm air (9). A step for the drying of fingerpads after exposure to the control or test substance therefore has not been included to avoid virus removal by the drying process itself.
This test method is not meant for use with surgical hand scrubs or preoperative skin preps.
The level of viable virus on each fingerpad after the drying of the inoculum should not be less than 104 infectious units which would permit the detection of up to a 4 log10 reduction in the infectivity titer of the virus by the test substance under the conditions of this test method.
1.1 Human skin is not known to carry viruses as a part of its resident microbiota. Hands transiently contaminated with viruses can however act as vehicles for the spread of many types of viral infections. Hand hygiene is meant to reduce the load of viruses and other transient microorganisms on hands thereby reducing the risk of disease transmission. Such reductions in the virus load may be due to a combination of virus inactivation and mechanical removal of infectious virus from the skin.
1.2 This test method is designed to determine the comparative virus-eliminating effectiveness of microbicidal or non-microbicidal formulations. This test method is not meant for use with surgical hand scrubs or preoperative skin preps.
Note 18212;The test method should be performed by persons with training in virology in facilities designed and equipped for work with infectious agents at biosafety level 2 (6).
1.3 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.
1.4 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 det......
The procedure should be used to test the degerming effectiveness of antimicrobial hand washing products used by health care personnel that are intended for frequent use and that are intended to reduce the level of contamination acquired through contact with contaminated objects or people.
Performance of these procedures requires the knowledge of regulations pertaining to the protection of human subjects (Ref 1).3
1.1 This test method can be used to determine the effectiveness of antimicrobial handwashing agents (including handrubs) in the reduction of transient bacterial flora with particular emphasis on the fingernail region.
1.2 A knowledge of microbiological techniques is required for these procedures.
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.
本標(biāo)準(zhǔn)適用于香皂、洗手液、沐浴劑等洗滌用品中三氯卡班含量的測定。
本標(biāo)準(zhǔn)適用于化妝品(膏霜、乳液、化妝水)和洗手液類產(chǎn)品中十一烯酸及其鋅鹽的測定。
本方法對十一烯酸及其鋅鹽的檢出限為12mg/kg(0.0012%),定量限為40mg/kg(0.004%)(均以酸計)。
本部分適用于商場、購物中心、超市等購物場所及相關(guān)設(shè)施,具體用于公共信息導(dǎo)向系統(tǒng)中的位置標(biāo)志、導(dǎo)向標(biāo)志、信息索引標(biāo)志、平面示意圖、街區(qū)導(dǎo)向圖、便攜印刷品及其他信息載體中的導(dǎo)向要素的設(shè)計。
本標(biāo)準(zhǔn)適用于城市、鄉(xiāng)村、旅游區(qū)和高諫公路服各區(qū)等新建、改建、擴(kuò)建供社會公眾使用的固定式公共廁所以及在公共場所內(nèi)設(shè)置的公共衛(wèi)生間的規(guī)劃、設(shè)計、建造、衛(wèi)生學(xué)評價?,F(xiàn)有公共廁所、學(xué)校公共廁所、單位內(nèi)部人員使用的公共廁所照執(zhí)行。
本文件適用于旅游景區(qū)、景區(qū)道路沿線、旅游度假區(qū)、旅游街區(qū)、旅游集散中心、鄉(xiāng)村旅游點等旅游活動區(qū)域和場所內(nèi)主要為游客服務(wù)的公共廁所。公共圖書館、文化館(站)、美術(shù)館、博物館等公共文化場所的公共廁所參照使用。
檢測資質(zhì)(部分)
檢測實驗室(部分)
合作客戶(部分)
檢測報告作用
1、可以幫助生產(chǎn)商識別產(chǎn)品的潛在問題或缺陷,并及時改進(jìn)生產(chǎn)工藝,保障產(chǎn)品的品質(zhì)和安全性。
2、可以為生產(chǎn)商提供科學(xué)的數(shù)據(jù),證明其產(chǎn)品符合國際、國家和地區(qū)相關(guān)標(biāo)準(zhǔn)和規(guī)定,從而增強(qiáng)產(chǎn)品的市場競爭力。
3、可以評估產(chǎn)品的質(zhì)量和安全性,確保產(chǎn)品能夠達(dá)到預(yù)期效果,同時減少潛在的健康和安全風(fēng)險。
4、可以幫助生產(chǎn)商構(gòu)建品牌形象,提高品牌信譽(yù)度,并促進(jìn)產(chǎn)品的銷售和市場推廣。
5、可以確定性能和特性以及元素,例如力學(xué)性能、化學(xué)性質(zhì)、物理性能、熱學(xué)性能等,從而為產(chǎn)品設(shè)計、制造和使用提供參考。
6、可以評估產(chǎn)品是否含有有毒有害成分,以及是否符合環(huán)保要求,從而保障產(chǎn)品的安全性。
7、可以為政府監(jiān)管部門提供獨立的數(shù)據(jù)和意見,支持政府制定有效的政策和措施,確保公眾的健康和安全。
檢測流程
1、中析研究所接受客戶委托,為客戶提供檢測服務(wù)
2、客戶可選擇寄送樣品或由我們的工程師進(jìn)行采樣,以確保樣品的準(zhǔn)確性和可靠性。
3、我們的工程師會對樣品進(jìn)行初步評估,并提供報價,以便客戶了解檢測成本。
4、雙方將就檢測項目進(jìn)行詳細(xì)溝通,并簽署保密協(xié)議,以保證客戶信息的保密性。在此基礎(chǔ)上,我們將進(jìn)行測試試驗.
5、在檢測過程中,我們將與客戶進(jìn)行密切溝通,以便隨時調(diào)整測試方案,確保測試進(jìn)度。
6、試驗測試通常在7-15個工作日內(nèi)完成,具體時間根據(jù)樣品的類型和數(shù)量而定。
7、出具檢測樣品報告,以便客戶了解測試結(jié)果和檢測數(shù)據(jù),為客戶提供有力的支持和幫助。
以上為洗手液檢測的檢測內(nèi)容,如需更多內(nèi)容以及服務(wù)請聯(lián)系在線工程師。