ANSI/ASTM F1671-1997
用病毒穿透率测试系统测试防护服材料抗血液携带病原体渗透性的方法

Test Method for Resistance of Protective Clothing Materials to Penetration by Blood-Borne Pathogens Using Viral Penetration as a Test System

ANSI/ASTM F1671-1997 发布历史

This test method is used to measure the resistance of materials used in protective clothing to penetration by blood-borne pathogens using a surrogate microbe under conditions of continuous liquid contact. Protective clothing material pass/fail determinations are based on the detection of viral penetration. This test method is not always effective in testing protective clothing materials having thick, inner liners which readily absorb the liquid assay fluid. This test method does not apply to all forms or conditions of blood-borne pathogen exposure. Users of the test method should review modes for worker/clothing exposure and assess the appropriateness of this test method for their specific applications. This test method has been specifically defined for modeling the viral penetration of Hepatitis (B and C) and Human Immunodeficiency Viruses transmitted in blood and other potentially infectious body fluids. Inferences for protection from other pathogens must be assessed on a case-by-case basis. This test method addresses only the performance of materials or certain material constructions (for example, seams) used in protective clothing and determined to be viral resistant. This test method does not address the design, overall construction and components, or interfaces of garments or other factors which may affect the overall protection offered by the protective clothing. The values stated in SI units or in other units shall be regarded separately as standard. The values stated in each system must be used independently of the other, without combining values in any way. 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.

ANSI/ASTM F1671-1997由美国国家标准学会 US-ANSI 发布于 1997。

ANSI/ASTM F1671-1997 在中国标准分类中归属于: C73 劳动防护用品，在国际标准分类中归属于: 13.340.10 防护服装,11.140 医院设备。

ANSI/ASTM F1671-1997的历代版本如下：

• 1997年 ANSI/ASTM F1671-1997 用病毒穿透率测试系统测试防护服材料抗血液携带病原体渗透性的方法

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标准号

ANSI/ASTM F1671-1997

发布日期

1997年

实施日期

废止日期

无

中国标准分类号

C73

国际标准分类号

13.340.10;11.140

发布单位

US-ANSI

被代替标准

ANSI/ASTM F1671-1996

适用范围

This test method is used to measure the resistance of materials used in protective clothing to penetration by blood-borne pathogens using a surrogate microbe under conditions of continuous liquid contact. Protective clothing material pass/fail determinations are based on the detection of viral penetration. This test method is not always effective in testing protective clothing materials having thick, inner liners which readily absorb the liquid assay fluid. This test method does not apply to all forms or conditions of blood-borne pathogen exposure. Users of the test method should review modes for worker/clothing exposure and assess the appropriateness of this test method for their specific applications. This test method has been specifically defined for modeling the viral penetration of Hepatitis (B and C) and Human Immunodeficiency Viruses transmitted in blood and other potentially infectious body fluids. Inferences for protection from other pathogens must be assessed on a case-by-case basis. This test method addresses only the performance of materials or certain material constructions (for example, seams) used in protective clothing and determined to be viral resistant. This test method does not address the design, overall construction and components, or interfaces of garments or other factors which may affect the overall protection offered by the protective clothing. The values stated in SI units or in other units shall be regarded separately as standard. The values stated in each system must be used independently of the other, without combining values in any way. 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.