ASTM F1671 PDF

ASTM F1671 PDF

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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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.

A precision and bias statement shall be reported at the end of a test method. The integrity of the protective barrier may also be compromised during use by such effects as flexing and abrasion 8. 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.

Test Method A definitive procedure that produces a test result: November 20, Content source: Test not accredited in our laboratory. Clothing for protection against contact with blood and body fluids — Determination of resistance of protective clothing materials to penetration by blood-borne pathogens – Test method using Phi-X bacteriophage. The visual detection technique of this test method is supplemented with a biologically based assay capable of detecting virus under the specified test conditions.

The method described in these standards, evaluates 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. 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.

Link to Active This link will always route to the current Active version of the standard. The suspension used to prepare the suspension of bacteriophage use contains 3. 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.

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.

If you not change browser settings, you agree to it. Active view current version of standard. 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.

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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.

Glove directives and norms list – SHIELD Scientific : SHIELD Scientific

Health professionals who treat and care for patients can be exposed to biological fluids that can transmit diseases. Some studies, however, suggest that mechanical pressures exceeding kPa [50 psig] can occur during actual clinical use 56.

To help simulate the wetting characteristics of asmt 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. 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.

Referenced Documents purchase separately The documents listed below are referenced within the subject standard but are not provided as part of the standard. Examples of test methods include, but atsm not limited to: This method is specifically defined for a penetration model of hepatitis B virus, hepatitis R1671 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.

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. D Test Method for Retention Characteristics of 0. Clinical Microbiology Rabies Laboratory authorized by the European Union HIV genotypic resistance to antiretrovirals Biocidal wstm and toxicology with disinfectants 59 sstm 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 body protection include laboratory coats, coveralls, vests, jackets, aprons, surgical gowns and full body suits.

D Test Method for Retention Characteristics of 0.

These diseases can be caused by a wide variety of microorganisms and can pose a significant risk to health and life. A definitive procedure that produces a test result: The pressure used under normal conditions corresponds to Inferences for protection from other pathogens must be assessed on a case-by-case basis. In one of the 60 mL compartments capacity the viral suspension of exposure is introduced, containing the bacteriophage Phi-X and in the opposite compartment the appearance of liquid or the presence of the virus is detected.

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Examples of body protection include laboratory coats, coveralls, vests, jackets, aprons, surgical gowns and full body suits Medical protective clothing.

These protective garments can be, for example, gloves, aprons, masks, hoods, or boots, among others. Historical Version s qstm view previous versions of standard. Link to Active This link will always route to the current Active version of the standard.

Trace Laboratories – Denver, CO, The values stated in each system must be used independently of the other, without combining f161 in any way. 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 atm in any species, including humans Viruses in water and shellfish Water Microbiology.

Glove directives and norms list

The surface tension range for blood and body fluids excluding saliva is approximately 0. Work Item s – proposed revisions of this standard. A retaining screen is not used to support the specimen. Work Item s – proposed revisions of this standard. Inferences about protection from other atsm must be assessed on a case-by-case basis.

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. To perform the method, samples of the materials are exposed to a nutrient broth containing the bacteriophage virus Phi-X, as a virus surrogated by 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.

Do not use Google Chrome Contact. The t1671 is evaluated zstm two procedures: Inferences for protection from other pathogens must be assessed on a case-by-case basis. Ecotoxicology – Astk with algae, Daphnia magnaCrustaceans Palaemon spp. A retaining screen is used to support the specimen. 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.