ASTM D3577 PDF

More D Material under this specification consists of Type I and Type II gloves, which shall be manufactured from any natural rubber compound, with the inside and outside surfaces of the gloves free of talc and with dimensions and physical properties that shall conform to the requirements specified. Tests for sterility, freedom from holes, physical dimensions, tensile strength, ultimate elongation, stress at elongation, powder-free residue, powder amount, protein content, and antigenic protein content shall be performed to assess the conformance of the rubber gloves with the requirements specified. This abstract is a brief summary of the referenced standard. It is informational only and not an official part of the standard; the full text of the standard itself must be referred to for its use and application. ASTM does not give any warranty express or implied or make any representation that the contents of this abstract are accurate, complete or up to date.

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A number in parentheses indicates the year of last reapproval. This standard has been approved for use by agencies of the U. Department of Defense. No other units of measurement are included in thisstandard. It is the responsibility of the userof this standard to establish appropriate safety and healthpractices and determine the applicability of regulatory limita-tions prior to use. Referenced Documents2. Materials and Manufacture4.

Pharmacopeia for Absorbable Dusting Powder may beapplied to the glove. Other lubricants may be used if theirsafety and efficacy have been previously established. Significance and Use5. The safe andproper use of rubber surgical gloves is beyond the scope of thisspecification.

The inspection levelsand acceptable quality levels AQL shall conform to thosespecified in Table 1, or as agreed between the purchaser and theseller, if the latter is more comprehensive. Performance Requirements7. Current edition approved Nov. Published December Originallyapproved in Pharmacopeia, latest edition, Mack Publishing Co.

United States Referee Test Methods8. Values of width per size other thanlisted shall meet the stated tolerance specified in Table 2. For referee tests, cutting the glove is necessary to obtainsingle-thickness measurements. Tests shall be conducted in accordance with Test MethodsD Die C is recommended. Test the gloves by either one ofthe following methods This methodshall be the condition for referee tests. If the glove sample is less than a whole glove, thenadjust the protein results to reflect the amount of protein in thewhole glove.

Four 4 is the factor for all inside and outside surface areas. Pharmacopeia and ISO Packaging and Package Marking ASTM International takes no position respecting the validity of any patent rights asserted in connection with any item mentionedin this standard. Users of this standard are expressly advised that determination of the validity of any such patent rights, and the riskof infringement of such rights, are entirely their own responsibility. This standard is subject to revision at any time by the responsible technical committee and must be reviewed every five years andif not revised, either reapproved or withdrawn.

Your comments are invited either for revision of this standard or for additional standardsand should be addressed to ASTM International Headquarters. Your comments will receive careful consideration at a meeting of theresponsible technical committee, which you may attend.

If you feel that your comments have not received a fair hearing you shouldmake your views known to the ASTM Committee on Standards, at the address shown below.

RAYMOND WACKS UNDERSTANDING JURISPRUDENCE PDF

ASTM D3577

More D The gloves shall be manufactured from any rubber polymer compound, with the inside and outside surfaces of the gloves free of talc and with dimensions and physical properties that shall conform to the requirements specified. Tests for sterility, freedom from holes, physical dimensions, tensile strength, ultimate elongation, stress at elongation, powder-free residue, powder amount, protein content, and antigenic protein content shall be performed to assess the conformance of the rubber gloves with the requirements specified. This abstract is a brief summary of the referenced standard. It is informational only and not an official part of the standard; the full text of the standard itself must be referred to for its use and application. ASTM does not give any warranty express or implied or make any representation that the contents of this abstract are accurate, complete or up to date.

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