檢測(cè)信息(部分)
- 該類產(chǎn)品的主要用途是什么?
洗手液主要用于手部清潔、殺菌或消毒,適用于家庭、醫(yī)療機(jī)構(gòu)、公共場(chǎng)所等場(chǎng)景,幫助減少病原微生物傳播。
- 檢測(cè)涵蓋哪些產(chǎn)品類型?
檢測(cè)范圍包括普通洗手液、抗菌洗手液、免洗洗手液、醫(yī)用消毒洗手液、兒童專用洗手液等不同分類產(chǎn)品。
- 檢測(cè)的核心內(nèi)容有哪些?
檢測(cè)涵蓋理化指標(biāo)、微生物指標(biāo)、毒理學(xué)安全性、有效成分含量及標(biāo)簽合規(guī)性等,確保產(chǎn)品符合國(guó)家標(biāo)準(zhǔn)或行業(yè)規(guī)范。
檢測(cè)項(xiàng)目(部分)
pH值:衡量產(chǎn)品酸堿度,避免對(duì)皮膚造成刺激。
有效成分含量:確保殺菌或消毒成分達(dá)到宣稱濃度。
總活性物含量:反映清潔能力的關(guān)鍵指標(biāo)。
重金屬殘留:檢測(cè)鉛、砷等有害物質(zhì),保障使用安全。
甲醇含量:防止有毒溶劑超標(biāo)。
菌落總數(shù):評(píng)估產(chǎn)品自身微生物污染風(fēng)險(xiǎn)。
大腸菌群:檢測(cè)致病菌污染情況。
金黃色葡萄球菌殺滅率:驗(yàn)證抗菌效果。
皮膚刺激性:通過(guò)實(shí)驗(yàn)評(píng)估產(chǎn)品對(duì)人體安全性。
穩(wěn)定性測(cè)試:考察產(chǎn)品保質(zhì)期內(nèi)性狀變化。
黏度:影響使用體驗(yàn)的物理特性。
總有效氯含量:針對(duì)含氯消毒成分的專項(xiàng)檢測(cè)。
乙醇濃度:免洗類產(chǎn)品的核心效能參數(shù)。
熒光增白劑:篩查非法添加物質(zhì)。
包裝密封性:防止產(chǎn)品泄漏或污染。
凈含量偏差:驗(yàn)證標(biāo)簽標(biāo)注準(zhǔn)確性。
起泡力:反映清潔效果的輔助指標(biāo)。
腐蝕性測(cè)試:評(píng)估對(duì)金屬或其他材質(zhì)的損害風(fēng)險(xiǎn)。
低溫穩(wěn)定性:檢測(cè)產(chǎn)品在寒冷環(huán)境下的性狀保持能力。
毒理實(shí)驗(yàn):通過(guò)動(dòng)物或體外試驗(yàn)評(píng)估長(zhǎng)期安全性。
檢測(cè)范圍(部分)
- 普通家用洗手液
- 醫(yī)用外科手消毒液
- 抗菌抑菌洗手液
- 免洗速干型洗手液
- 兒童溫和型洗手液
- 植物提取物配方洗手液
- 含氯己定洗手液
- 乙醇基免洗凝膠
- 季銨鹽類消毒洗手液
- 泡沫型洗手液
- 甘油保濕型洗手液
- 敏感肌專用洗手液
- 食品加工行業(yè)專用洗手液
- 公共場(chǎng)所大容量裝洗手液
- 便攜式單片包裝洗手液
- 抗病毒宣稱洗手液
- 含天然精油成分洗手液
- 低敏無(wú)香型洗手液
- 醫(yī)院ICU專用消毒液
- 含過(guò)氧化氫成分洗手液
檢測(cè)儀器(部分)
- 高效液相色譜儀
- 氣相色譜質(zhì)譜聯(lián)用儀
- 紫外可見(jiàn)分光光度計(jì)
- 原子吸收光譜儀
- 微生物培養(yǎng)箱
- 生物安全柜
- pH計(jì)
- 旋轉(zhuǎn)粘度計(jì)
- 恒溫恒濕試驗(yàn)箱
- 電子天平
檢測(cè)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(cè)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(cè)定。
本方法對(duì)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(jì))。
本部分適用于商場(chǎng)、購(gòu)物中心、超市等購(gòu)物場(chǎng)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(jì)。
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(huì)公眾使用的固定式公共廁所以及在公共場(chǎng)所內(nèi)設(shè)置的公共衛(wèi)生間的規(guī)劃、設(shè)計(jì)、建造、衛(wèi)生學(xué)評(píng)價(jià)?,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?qǐng)?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(diǎn)等旅游活動(dòng)區(qū)域和場(chǎng)所內(nèi)主要為游客服務(wù)的公共廁所。公共圖書(shū)館、文化館(站)、美術(shù)館、博物館等公共文化場(chǎng)所的公共廁所參照使用。

檢測(cè)資質(zhì)(部分)
北京中科光析科學(xué)技術(shù)研究所旗下實(shí)驗(yàn)室擁有CMA檢驗(yàn)檢測(cè)資質(zhì)證書(shū)以及CNAS證書(shū)和ISO證書(shū)以及高新技術(shù)企業(yè)證書(shū)和AAA級(jí)信用企業(yè)證書(shū)和山東省國(guó)防經(jīng)濟(jì)發(fā)展促進(jìn)會(huì)會(huì)員證書(shū)等多項(xiàng)榮譽(yù)資質(zhì)。
檢測(cè)優(yōu)勢(shì)
檢測(cè)實(shí)驗(yàn)室(部分)
北京中科光析科學(xué)技術(shù)研究所旗下實(shí)驗(yàn)室擁有物理試驗(yàn)室、機(jī)械實(shí)驗(yàn)室、化學(xué)試驗(yàn)室、生物實(shí)驗(yàn)室以及微生物實(shí)驗(yàn)室等多個(gè)檢驗(yàn)檢測(cè)實(shí)驗(yàn)室,為多行業(yè)的檢驗(yàn)檢測(cè)服務(wù)提供了堅(jiān)固的支撐,檢測(cè)儀器齊全,能滿足多行業(yè)客戶檢測(cè)需求。
合作客戶(部分)
檢測(cè)報(bào)告作用
1、可以幫助生產(chǎn)商識(shí)別產(chǎn)品的潛在問(wèn)題或缺陷,并及時(shí)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(guó)際、國(guó)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(chǎng)競(jìng)爭(zhēng)力。
3、可以評(píng)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(shí)減少潛在的健康和安全風(fēng)險(xiǎn)。
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(chǎng)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(jì)、制造和使用提供參考。
6、可以評(píng)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。
檢測(cè)流程
1、中析研究所接受客戶委托,為客戶提供檢測(cè)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(huì)對(duì)樣品進(jìn)行初步評(píng)估,并提供報(bào)價(jià),以便客戶了解檢測(cè)成本。
4、雙方將就檢測(cè)項(xiàng)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(cè)試試驗(yàn).
5、在檢測(cè)過(guò)程中,我們將與客戶進(jìn)行密切溝通,以便隨時(shí)調(diào)整測(cè)試方案,確保測(cè)試進(jìn)度。
6、試驗(yàn)測(cè)試通常在7-15個(gè)工作日內(nèi)完成,具體時(shí)間根據(jù)樣品的類型和數(shù)量而定。
7、出具檢測(cè)樣品報(bào)告,以便客戶了解測(cè)試結(jié)果和檢測(cè)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(cè)的檢測(cè)內(nèi)容,如需更多內(nèi)容以及服務(wù)請(qǐng)聯(lián)系在線工程師。