ASTM D 3577-09 橡胶医用手套标准规范

Designation:D3577–09

Standard Speciﬁcation for

Rubber Surgical Gloves1

This standard is issued under theﬁxed designation D3577;the number immediately following the designation indicates the year of original adoption or,in the case of revision,the year of last revision.A number in parentheses indicates the year of last reapproval.A superscript epsilon(´)indicates an editorial change since the last revision or reapproval.

This standard has been approved for use by agencies of the Department of Defense.

1.Scope

1.1This speciﬁcation covers certain requirements for pack-aged sterile rubber surgical gloves used in conducting surgical procedures.

1.2The values stated in SI units are to be regarded as standard.No other units of measurement are included in this standard.

1.3The following safety hazards caveat pertains only to the test method portion,Section8,of this speciﬁcation:This standard does not purport to address all of the safety concerns, if any,associated with its use.It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limita-tions prior to use.

2.Referenced Documents

2.1ASTM Standards:2

D412Test Methods for Vulcanized Rubber and Thermo-plastic Elastomers—Tension

D573Test Method for Rubber—Deterioration in an Air Oven

D3767Practice for Rubber—Measurement of Dimensions D5151Test Method for Detection of Holes in Medical Gloves

D5712Test Method for Analysis of Aqueous Extractable Protein in Natural Rubber and Its Products Using the Modiﬁed Lowry Method

D6124Test Method for Residual Powder on Medical Gloves

D6499Test Method for The Immunological Measurement of Antigenic Protein in Natural Rubber and its Products 2.2Other Documents:

ISO2859Sampling Procedures and Tables for Inspection by Attributes3

U.S.Pharmacopeia4

3.Classiﬁcation

3.1Type1—Gloves compounded primarily from natural rubber latex.

3.2Type2—Gloves compounded from a rubber cement or from synthetic rubber latex.

4.Materials and Manufacture

4.1Any rubber polymer compound that permits the glove to meet the requirements of this speciﬁcation.

4.2A lubricant that meets the current requirements of the U.S.Pharmacopeia for Absorbable Dusting Powder may be applied to the glove.Other lubricants may be used if their safety and efficacy have been previously established.

4.3The inside and outside surface of the rubber surgical gloves shall be free of talc.

5.Signiﬁcance and Use

5.1The speciﬁcation is intended as a reference to the performance and safety of rubber surgical gloves.The safe and proper use of rubber surgical gloves is beyond the scope of this speciﬁcation.

6.Sampling

6.1For referee purposes,gloves shall be sampled and inspected in accordance with ISO2859.The inspection levels and acceptable quality levels(AQL)shall conform to those speciﬁed in Table1,or as agreed between the purchaser and the seller,if the latter is more comprehensive.

7.Performance Requirements

7.1Gloves,sampled in accordance with Section6,shall meet the following referee performance requirements:

7.1.1Comply with requirements for sterility when tested in accordance with8.2.

质粒拯救1This speciﬁcation is under the jurisdiction of ASTM Committee D11on Rubber and is the direct responsibility of Subcommittee D11.40on Consumer Rubber Products.

Current edition approved Jan.1,2009.Published February2009.Originally approved in1977.Last previous edition approved in2006as D3577–06.

2For referenced ASTM standards,visit the ASTM website,,or

contact ASTM Customer Service at For Annual Book of ASTM Standards volume information,refer to the standard’s Document Summary page on the ASTM website.

3Available from American National Standards Institute,25West43rd St.,4th Floor,New York,NY10036.

4U.S.Pharmacopeia,latest edition,Mack Publishing Co.,Easton,PA19175.

7.1.2Be free from holes when tested in accordance with 8.3.7.1.3Have consistent physical dimensions in accordance with 8.4.

7.1.4Have acceptable physical property characteristics in accordance with 8.5.

7.1.5Have a powder residue limit of 2.0mg in accordance with 8.6.

Have a recommended aqueous soluble protein content limit of 200µg/dm 2in accordance with 8.7and Annex A1or have a recommended antigenic protein content limit of 10µg/dm 2in accordance with 8.9and Annex A2.

7.1.7Have a recommended maximum powder limit of 15mg/dm 2in accordance with 8.8.

8.Referee Test Methods

8.1The following tests shall be conducted to assure the requirements of Section 7as prescribed in Table 1:

8.2Sterility Test —Testing for sterility shall be conducted in accordance with the latest edition of the U.S.Pharmacopeia .8.3Freedom from Holes —Testing for freedom from holes shall be conducted in accordance with Test Method D 5151.8.4Physical Dimensions Test :

8.4.1The gloves shall comply with the dimension require-ments speciﬁed in Table 2.

8.4.2The length shall be expressed in millimetres as mea-sured from the tip of the second ﬁnger to the outside edge of the cuff.

8.4.3The width of the palm shall be expressed in millime-tres as measured at a level between the base of the index ﬁnger and the base of the thumb.Values of width per size other than listed shall meet the stated tolerance speciﬁed in Table 2.

8.4.4The minimum thickness shall be expressed in milli-metres as speciﬁed in Table 2when using a dial micrometer described in Practice D 3767and in the locations indicated on Fig.1.For referee tests,cutting the glove is necessary to obtain single-thickness measurements.

8.4.5Precision and Bias —The precision and bias of mea-suring glove dimensions are as speciﬁed in Practice D 3767.8.5Physical Requirements Test :

8.5.1Before and after accelerated aging,the gloves shall conform to the physical requirements speciﬁed in Table 3.Tests shall be conducted in accordance with Test Methods D 412.

8.5.2Accelerated aging tests shall be conducted in accor-dance with Test Method D 573.Test the gloves by either one of the following methods:

8.5.2.1After being subjected to a temperature of 7062°C for 16662h,the tensile strength and ultimate elongation shall not be less than the values speciﬁed in Table 3.This method shall be the condition for referee tests.

8.5.2.2After being subjected to a temperature of 10062°C for 2260.3h,the tensile strength and ultimate elongation shall not be less than the values speciﬁed in Table 3.

8.5.3Precision and Bias —The precision and bias of deter-mining tensile strength and ultimate elongation of gloves are as speciﬁed in Test Methods D 412.8.6Powder Free Gloves :

8.6.1Determine the powder residue using Test Method D 6124.mum-147

横孔螺母

8.7Aqueous Extractable Protein Content :

8.7.1Determine the aqueous extractable protein (µg/mL)using Test Method D 5712for each glove sample tested.

8.7.2Determine the total µg of aqueous extractable protein in each glove sample by multiplying the result from 8.7.1by the total volume of extractant used for that speciﬁc glove sample.If the glove sample is less than a whole glove,then adjust the protein results to reﬂect the amount of protein in the whole glove.

8.7.3Determine the square decimetres for the glove size.Multiply the minimum length and nominal width found in Table 2and convert to dm 2using (dm 2/mm 2)(mm 2/10000).Four (4)is the factor for all inside and outside surface areas.8.7.4Determine the aqueous extractable protein content of a glove sample by dividing the result from 8.7.2(total µg of protein)by 8.7.3(total surface area of glove).

TABLE 1Performance Requirements

Characteristic Related Defects Inspection Level

AQL Sterility

fails sterility A

N/A Freedom from holes holes

I 1.5Physical dimensions length,width,and thickness

S-2 4.0Physical properties before aging,after accel-erated aging

S-2 4.0Powder Free Residue Exceeds Maximum Limit N=5N/A Protein Content Exceeds Recommended Maximum Limit

N=3N/A Powder Amount Exceeds Recommended Maximum Limit

N=2N/A Antigenic Protein Content

Exceeds Recommended Maximum Limit

N=1

N/A

See U.S.Pharmacopeia .

TABLE 2Dimensions and Tolerances

Designation Size

Tolerance 51⁄2661⁄2771⁄2881⁄29Length,mm 245265265265265265265265min Width,mm 70

102

怎么自制纳米胶108

114

Thickness,mm:Finger 0.10min Palm 0.10min Cuff

0.10

min

--```,,,`,``,,`,,``````````,,,`-`-`,,`,,`,`,,`---

8.7.5If the sample is more than one (1)glove,use the

average µg/dm 2of protein for the number of gloves tested in the sample.

8.8Powdered Gloves :

8.8.1Determine the recommended maximum powder limit using Test Method D 6124for powdered gloves.

8.8.2Determine the square decimeters for the glove size as in 8.7.3.

8.9Antigenic Protein Content :

8.9.1Determine the extractable antigenic protein (µg/mL)using Test Method D 6499for each glove sample tested.

8.9.2Determine the total microgram of extractable anti-genic protein in each glove sample by multiplying the result from 8.9.1by the total volume of extractant used for that speciﬁc glove sample.

8.9.3Determine the square decimeter for the glove size as in 8.7.3.

8.9.4Determine the extractable antigenic protein content of a glove sample by dividing the result from 8.9.2(total microgram of antigenic protein)by 8.9.3(total surface area of glove).9.Acceptance

9.1Gloves will be considered to meet the referee perfor-mance requirements when test results conform to the require-ments prescribed in Table 1.

9.2Retests or reinspections are permissible under the pro-visions of the U.S.Pharmacopeia and ISO 2859.10.Packaging and Package Marking

10.1Packaging —Packaging shall be provided to maintain sterility after sterilization during shipping and storage and permit opening without contamination of the gloves.10.2Marking

FIG.1Location of Thickness Measurements

TABLE 3Physical Requirements

Type Before Aging After Accelerated Aging

Tensile Strength Ultimate Elongation Stress at 500%Elongation Tensile Strength Ultimate Elongation I 24MPa,min 750%min 5.5MPa,max 18MPa,min 560%min II

17MPa,min

650%min

7.0MPa,max

12MPa,min

490%

min

--```,,,`,``,,`,,``````````,,,`-`-`,,`,,`,`,,`---

10.2.1Gloves shall have an appropriate marking or be color-coded to designate size.

10.2.2Inner wrappers or wallets,if used,shall bear a size marking to be located on the outside of the wallet or wrapper.

10.2.3Packages shall bear markings for the contents to include the glove size,instructions for opening,the legend “sterile,”and a manufacturing lot number.

10.2.4The outermost case shall be labeled on one or more end panels with the glove size,the legend“sterile,”and a manufacturing lot number.

10.2.5All levels of packaging shall conform to all appro-priate government labeling regulations.

11.Keywords

11.1gloves;rubber;surgical

ANNEXES (Mandatory Information) A1.PROTEIN CONTENT

智能感应垃圾桶A1.1The current assay precision is large enough that only a recommended limit can be considered.

A1.2Consideration should be given to the relative repeat-ability and reproducibility when reporting test method results.

A1.3Reasonable allowance should be given for test results in excess of the recommended limit until greater precision of the method can be attained.

A2.ANTIGENIC PROTEIN CONTENT

A2.1The current assay precision is large enough that only a recommended limit can be considered.

受话器

A2.2Consideration should be given to the relative repeat-ability and reproducibility when reporting test method results.

A2.3A pooled sample from three individual NR specimens or products as extracted in Test Method D5712is permitted for use as the extraction sample.

ASTM International takes no position respecting the validity of any patent rights asserted in connection with any item mentioned in this standard.Users of this standard are expressly advised that determination of the validity of any such patent rights,and the risk of 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 everyﬁve years and if not revised,either reapproved or withdrawn.Your comments are invited either for revision of this standard or for additional standards and should be addressed to ASTM International Headquarters.Your comments will receive careful consideration at a meeting of the responsible technical committee,which you may attend.If you feel that your comments have not received a fair hearing you should make your views known to the ASTM Committee on Standards,at the address shown below.

This standard is copyrighted by ASTM International,100Barr Harbor Drive,PO Box C700,West Conshohocken,PA19428-2959, United States.Individual reprints(single or multiple copies)of this standard may be obtained by contacting ASTM at the above address or at610-832-9585(phone),610-832-9555(fax),or (e-mail);or through the ASTM website

().

--```,,,`,``,,`,,``````````,,,`-`-`,,`,,`,`,,`---

本文发布于:2024-09-22 10:31:19，感谢您对本站的认可！

本文链接：https://www.17tex.com/tex/3/320682.html

上一篇：AClean一次性医用手套的小知识

下一篇：一次性使用聚氯乙烯医用检查手套产品技术标准2023年