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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ASTM International – Standard References for ASTM F / FM – 13
Historical Version f16771 – view previous versions of standard. Trace Laboratories – Denver, CO, Active view current version of standard. 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. Work Item s – proposed revisions of this standard.
These diseases can be caused by a wide variety of microorganisms and can pose a significant risk to health and life. A precision and bias statement shall be reported at the end of a test method. The manufacturer must indicate the possibility that the material under test can be altered by thermal r1671 wet sterilizationso as not to do so in the event that it can be altered.
Inferences for protection from other pathogens must be assessed on a case-by-case basis. Inferences for protection from other pathogens must be assessed on a case-by-case basis. The possible alterations of the protective material due to physical, chemical or thermal effects should be taken into account, since in this case they would negatively influence the behavior of the material, so that in case it can occur, the tests should be carried out before exposures to such material, physical, chemical or thermal conditions that may deteriorate it.
The values stated in each system must be used independently of the other, without combining values in any way. This includes bullet-proof clothing, general protective clothing and full body ensembles that protect from cuts, radiation, temperature extremes, hot splashes from molten metals and other hot liquids, potential impacts from tools, machinery and materials and hazardous chemicals.
Prewetting agents, such as alcohol, and contaminating agents, such as perspiration, may also compromise the integrity of the protective barrier. The suspension used to prepare the suspension of bacteriophage use contains 3.
Materials passing Test Method F should then be tested against bacteriophage penetration using this test method to verify performance. Any visual or virological evidence of penetration will indicate the inability of the material to resist penetration. Ecotoxicology – Test with algae, Daphnia magnaCrustaceans Palaemon spp.
A retaining screen is used to support the specimen. If you not change browser settings, you agree to it. Examples of body protection include laboratory coats, coveralls, vests, jackets, aprons, surgical gowns and full body suits. 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.
The test includes a positive control consisting of a membrane with a pore slightly greater than the diameter of the bacteriophage 0. Genetic Testing – Human gene mutations diseases, neoplasias and pharmacogenetics Clostridium botulinum tests Molecular veterinary microbiology Tests for movement of animals South Africa, Australia, India, New Zealand Food microbiology Viruses in water and shellfish Water Microbiology Zebra mussel Dreissena polymorphaother mussels and intermediate hosts molluscs Bulinus spp.
In case a non-sterile material is used, the test will include the corresponding controls to exclude the presence of the bacteriophage in the materials evaluated.
Glove directives and norms list
The values stated in each system must be used independently of the other, without combining aetm in any way. 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. Test Method A definitive procedure that produces a test result: A retaining screen is not used to support the specimen. These protective garments can be, for example, gloves, aprons, masks, f11671, or boots, among others.
Glove directives and norms list – SHIELD Scientific : SHIELD Scientific
To perform the method, samples of the materials are exposed to a nutrient broth containing the bacteriophage virus Phi-X, as a virus surrogated f1617 its characteristics similar in size to the hepatitis C virus, and by extension to the hepatitis B virus and of human immunodeficiency virus these viruses are not used because of their difficulty to be cultured in laboratories.
The test is performed in a chamber of two compartments, separated by the material evaluated. Do not use Google Chrome Contact.
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. Link to Active This link will always route to the current Active version of the standard. The surface tension range for blood and body fluids excluding saliva is approximately 0.
Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content. 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.
Inferences about protection from other pathogens must be assessed on a case-by-case basis. Some studies, however, suggest that mechanical pressures exceeding kPa [50 psig] can occur during actual clinical use 56.
A definitive procedure that produces a test result: 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: Examples of test methods include, but are not limited to: D1671 test method is normally used to evaluate specimens from individual finished items of protective clothing and individual samples of materials that are candidates for items of protective clothing.
This is accomplished by adding surfactant to the Phi-X Bacteriophage nutrient broth. This test method is used to measure the resistance of materials used in protective clothing to f167 by blood-borne pathogens ff1671 a surrogate microbe under conditions of continuous liquid contact.
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.
Ecotoxicology c1671 Test with algae, Daphnia magna and fishes Environmental microbiology Plants microbiology Marine biotoxins toxins in fish and bivalve molluscs DSP, PSP, NSP, ciguatoxins Aquaculture infectious diseases Molecular diagnosis Fertilizers Microbiology Paternity tests in any species, including humans Identification of animal species and sex in meat or fish products. D Test Method for Asstm Characteristics of 0.