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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The test is carried out observing the penetration of liquid without pressure for 5 minutes, followed by 1 minute at the 1f671 pressure 1. This 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.

Glove directives and norms list

To protect themselves from infectious agents transmitted by blood, health personnel should wear protective clothing made of materials that prevent microbes or viruses from passing through. Referenced Documents purchase separately The documents listed below are referenced within the subject standard but are not provided as part of the standard.

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.

Link to Active This link will always route to the current Active version of the standard. Materials passing Test Method F should then be tested against bacteriophage penetration using this test method to verify performance.

This hydrostatic pressure has been documented to discriminate between protective clothing material performance and correlate with visual penetration results that are obtained with a human factors validation 4.

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D Test Method for Retention Characteristics of 0. Ecotoxicology – Test with algae, Daphnia magnaCrustaceans Palaemon spp. 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.

This is accomplished by adding surfactant to the Phi-X Bacteriophage nutrient broth. A retaining screen is used to support the specimen.

Inferences for protection from other pathogens must be assessed on a case-by-case basis.

Health professionals who treat and care for patients can be exposed to biological fluids that can transmit diseases. A retaining screen is not used to support the specimen. The visual detection technique of this test method is supplemented with a biologically based assay capable of detecting virus under the specified test conditions.

f16711 This 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. 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.

PPE-Info – Standard Details

A definitive procedure that produces a test result: Historical Version s – view previous versions of standard. 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. Do not use Google Chrome Contact. Test Method A definitive procedure that produces a test result: The type must be specified.

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. Prewetting agents, such as alcohol, and contaminating agents, such as perspiration, may also compromise the integrity of the protective barrier.

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The test is performed in a chamber of two compartments, separated by the material evaluated. Any visual or virological evidence of penetration will indicate the inability of the material to resist penetration. Work Item s – proposed revisions of this standard. 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.

Active view current version of standard.

These diseases can be caused by a wide variety of microorganisms and can pose a significant risk to health and life. To help simulate the wetting characteristics of blood and body fluids, the surface tension of the Phi-X Bacteriophage challenge suspension is adjusted to f161 the lower end of this surface tension range. The exposure is carried out for a specified time and under a selected pressure. This standard does not purport to address all of the safety concerns, if any, associated with its use.

Test not accredited in our laboratory. Trace Laboratories – Denver, CO, This test method is based on Test Method F for measuring resistance of chemical protective clothing materials to penetration by liquids. Ff1671 manufacturer must indicate the possibility that the material under test can be altered by thermal treatment wet sterilizationso as not to do so in the event that it can be altered.

November 20, Page last v1671 Test Method F uses the same penetration test cell and technique, but exposes material specimens awtm synthetic blood with visual detection of liquid penetration.