ASTM F / FM – Standard Test Method for Resistance of Materials Used in Protective Clothing to Penetration by Blood-Borne Pathogens Using. ASTM F / FM – ASTM International (ASTM). Title. “Standard Test Method for Resistance of Materials Used in Protective Clothing to Penetration by . STANDARD USED: ASTM F, Standard Test Method for Resistance of Materials Used in Protective. Clothing to Penetration by Blood-Borne Pathogens .
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Link to Active This link will always route to the current Active version of the standard. This r1671 is specifically defined for a penetration model of hepatitis B virus, hepatitis C virus and human immunodeficiency virus, and it is considered by extension that if it resists penetration by these viruses, it will also resist penetration by larger microorganisms like bacteria.
Genetic testing – Human gene mutations diseases, neoplasias and pharmacogenetics Biocidal activities with disinfectants 59 accredited tests Cosmetics Microbiology Laboratory of control authorized by AEMPS 8 accredited tests Toxicology – Biological evaluation of medical devices; Cosmetics; Biocides; MPCA products 19 accredited tests Clostridium botulinum tests Paternity tests in any species, including humans Viruses in water and shellfish Water Microbiology.
This standard does not aatm to address all of the safety concerns, if any, associated with its use. Health professionals who treat and care for patients can be exposed to biological fluids that can transmit diseases. Test not accredited in our laboratory.
Therefore, it is important to understand that this test method does not simulate all the physical stresses and pressures that might be exerted on protective clothing materials during actual use.
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Ecotoxicology – Test with algae, Daphnia magnaCrustaceans Palaemon spp. November 20, Content source: The material used in the protective garment will pass or fail in the test, depending on whether it resists penetration is not traversed or allows it to be traversed. The values stated in each system must be used independently of the other, without combining values in any way. Examples of test methods include, but are not limited to: 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 method is evaluated by two procedures: Clinical Microbiology Rabies Laboratory authorized by the European Union HIV genotypic resistance to antiretrovirals Biocidal activities and toxicology with disinfectants 59 accredited tests Toxicology – Biological evaluation of medical devices; MPCA products 19 accredited tests Cosmetic Microbiology Laboratory of control authorized by AEMPS 8 accredited tests Neutralizing antibodies in human immunoglobulins 3 accredited tests News on viruses: The surface tension range for blood and body fluids excluding saliva is approximately 0.
Additional tests should be considered that assess the impact of storage conditions and shelf life on disposable products and the impact of laundering and sterilization on reusable products. The method described in these standards, asttm the effectiveness of materials used in the manufacture of protective garments against bloodborne pathogens using a surrogate virus suspended in a liquid, simulating the spontaneous contact conditions in a sanitary environment.
Examples of body protection include laboratory coats, coveralls, vests, jackets, aprons, surgical gowns and full body suits Medical protective clothing. 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.
If these conditions are of concern, the performance of protective clothing materials should be evaluated for Phi-X Bacteriophage penetration following an appropriate preconditioning technique representative of the expected conditions of use.
Inferences for asrm from other pathogens must be assessed on a case-by-case basis. To help simulate the wetting characteristics of blood and body fluids, the surface tension of the Phi-X Bacteriophage challenge suspension is adjusted to approximate the lower end of this surface tension range.
Glove directives and norms list
Work Item s – proposed revisions of this standard. Please see the full standard for complete details. The pieces of the evaluated materials are recommended to have about 75 mm on each side, of which a 57 mm diameter circle is exposed. The visual detection technique of this test method is supplemented f671 a biologically based assay capable of detecting virus under the specified test conditions.
These protective garments can be, for example, gloves, aprons, masks, hoods, or boots, among others. Because of the length of time required to complete this method, it may not be suitable for use as a material or protective clothing quality control or quality assurance procedure.
The values stated in each system must be used independently of the other, without combining values in any way.
Glove directives and norms list – SHIELD Scientific : SHIELD Scientific
Referenced Documents purchase separately F671 documents listed below are referenced within the subject standard but are not provided as part of the standard. Work Item s – proposed revisions of this standard. The type must be specified. The integrity of the protective barrier may also be compromised during use by such effects as flexing and abrasion 8.
The resulting surface tension of the Phi-X Bacteriophage challenge suspension is approximately 0.