1、Designation:D631910(Reapproved 2015)Standard Specification forNitrile Examination Gloves for Medical Application1This standard is issued under the fixed designation D6319;the number immediately following the designation indicates the year oforiginal adoption or,in the case of revision,the year of la
2、st revision.A number in parentheses indicates the year of last reapproval.Asuperscript epsilon()indicates an editorial change since the last revision or reapproval.1.Scope1.1 This specification covers certain requirements for nitrilerubber gloves used in conducting medical examinations anddiagnostic
3、 and therapeutic procedures.1.2 This specification covers nitrile rubber examinationgloves that fit either hand,paired gloves,and gloves by size.Italso provides for packaged sterile or nonsterile or bulk non-sterile nitrile rubber examination gloves.1.3 This specification is similar to that of Speci
4、ficationD3578 for rubber examination gloves.1.4 The values stated in SI units are to be regarded asstandard.No other units of measurement are included in thisstandard.2.Referenced Documents2.1 ASTM Standards:2D412 Test Methods for Vulcanized Rubber and Thermoplas-tic ElastomersTensionD573 Test Metho
5、d for RubberDeterioration in an AirOvenD3578 Specification for Rubber Examination GlovesD3767 Practice for RubberMeasurement of DimensionsD5151 Test Method for Detection of Holes in MedicalGlovesD6124 Test Method for Residual Powder on Medical Gloves2.2 ISO Standard:ISO 2859 Sampling Procedures and
6、Tables for Inspection byAttributes32.3 Other Documents:U.S.Pharmacopeia43.Significance and Use3.1 The specification is intended as a referee procedure forevaluating the performance and safety of nitrile rubber exami-nation gloves.The safe and proper use of nitrile rubberexamination gloves is beyond
7、the scope of this specification.4.Material4.1 Any nitrile rubber polymer compound may be used thatpermits the glove to meet the requirements of this specification.4.2 A lubricant that meets the current requirements of theU.S.Pharmacopeia for absorbable dusting powder may beapplied to the glove.Other
8、 lubricants may be used if theirsafety and efficacy have been previously established.4.3 The inside and outside surface of the nitrile rubberexamination gloves shall be free of talc.5.Sampling5.1 For referee purposes,gloves shall be sampled fromfinished product,after sterilization when labeled steri
9、le,andinspected in accordance with ISO 2859.The inspection levelsand acceptable quality levels(AQL)shall conform to thosespecified in Table 1,or as agreed upon between the purchaserand the seller,if the latter is more comprehensive.6.Performance Requirements6.1 Gloves,sampled in accordance with Sect
10、ion 5,shallmeet the following referee performance requirements:6.1.1 Product comply with requirements for sterility whentested in accordance with 7.2 when labeled sterile.6.1.2 Shall comply with freedom from holes when tested inaccordance with 7.3.6.1.3 Have consistent physical dimensions in accorda
11、ncewith 7.4.6.1.4 Have acceptable physical property characteristics inaccordance with 7.5.6.1.5 Have a powder residue limit of 2.0 mg in accordancewith 7.66.1.6 Have a recommended maximum powder limit of 10mg/dm2in accordance with 7.7.7.Referee Test Methods7.1 The following tests shall be conducted
12、to ensure therequirements of Section 6,as prescribed in Table 1:1This specification is under the jurisdiction ofASTM Committee D11 on Rubberand is the direct responsibility of Subcommittee D11.40 on Consumer RubberProducts.Current edition approved Nov.1,2015.Published December 2015.Originallyapprove
13、d in 1999.Last previous edition approved in 2005 as D6319 10.DOI:10.1520/D6319-10R15.2For referenced ASTM standards,visit the ASTM website,www.astm.org,orcontact ASTM Customer Service at serviceastm.org.For Annual Book of ASTMStandards volume information,refer to the standards Document Summary page
14、onthe ASTM website.3Available from American National Standards Institute,25 W.43rd St.,4thFloor,New York,NY 10036.4U.S.Pharmacopeia,latest edition,Mack Publishing Co.,Easton,PA 19175.Copyright ASTM International,100 Barr Harbor Drive,PO Box C700,West Conshohocken,PA 19428-2959.United States1 7.2 Ste
15、rility TestTesting for sterility shall be conducted inaccordance with the latest edition of the U.S.Pharmacopeia.7.3 Freedom from HolesTesting for freedom from holesshall be conducted in accordance with Test Method D5151.7.4 Physical Dimensions Test:7.4.1 The gloves shall comply with the dimension r
16、equire-ments prescribed in Table 2.7.4.2 The length shall be expressed in millimetres as mea-sured from the tip of the middle finger to the outside edge ofthe cuff.7.4.3 The width of the palm shall be expressed in millime-tres as measured at a level between the base of the index fingerand the base of the thumb.Values of width per size other thanlisted shall meet the stated tolerance specified in Table 2.7.4.4 The minimum thickness shall be expressed in milli-metres as specified in Table 2 when u