G44 胶乳制品 标准查询与下载

JIS T 9111-7:2000 橡胶避孕套.第7部分:耐热处理

この規格は，包装したラテックス製コンドーム(以下，コンドームという。)の貯蔵中の耐劣化性の測定方法について規定する。

Rubber condoms -- Part 7: Oven conditioning

JIS T 9111-1:2000 橡胶避孕套.第1部分:要求

この規格は，避妊の目的及び性感染症予防の補助として設計され，また，天然ゴムラテックス製で消費者に供給される男性用コンドーム(以下，コンドームという。)に対する要求事項について規定する。

Rubber condoms -- Part 1: Requirements

JIS T 9111-2:2000 橡胶避孕套.第2部分:长度的测定

この規格は，ラテックス製コンドーム(以下，コンドームという。)の長さの測定方法について規定する。

Rubber condoms -- Part 2: Determination of length

JIS T 9111-3:2000 橡胶避孕套.第3部分:宽度的测定

この規格は，ラテックス製コンドーム(以下，コンドームという。)の折幅の測定方法について規定する。

Rubber condoms -- Part 3: Determination of width

JIS T 9111-5:2000 橡胶避孕套.第5部分:孔的试验.水渗漏试验

この規格は，ラテックス製コンドーム(以下，コンドームという。)に水を満たし，その漏れを観察することによってコンドームの穴を検出する試験方法について規定する。

Rubber condoms -- Part 5: Testing for holes -- Water leak test

JIS T 9111-9:2000 橡胶避孕套.第9部分:拉伸特性的测定

この規格は，ラテックス製コンドーム(以下，コンドームという。)の引張特性の測定方法について規定する。

Rubber condoms -- Part 9: Determination of tensile properties

JIS T 9111-10:2000 橡胶避孕套.第10部分:包装和标签

この規格は，ラテックス製コンドーム(以下，コンドームという。)の包装と表示に対する要求事項を規定する。

Rubber condoms -- Part 10: Packaging and labelling

JIS T 9115:2000 一次性使用的橡胶检验手套

この規格は，手術を除いた検査，検診，治療行為及び汚染された医療材料を取り扱う場合患者及ぴ使用者を交差感染から守るために使用する滅菌及び未滅菌の使い捨て形式のゴム手袋(以下，手袋という。)について規定する。また。この規格は，手袋の表面が平滑なもの及び表面の一部又は全面が粗面の手袋にも適用する。

Single-use rubber examination gloves

JIS T 9113:2000 一次性使用的牙科橡胶手套

この規格は，歯科で，診察，治療及び処置に用いる場合，患者及び使用者を交差感染から守るために使用する滅菌及び未滅菌の使い捨て形式のゴム手袋(以下，手袋という。)について規定する。

Single-use rubber gloves for dentistry

JIS T 9114:2000 一次性使用的牙科聚氯乙烯手套

この規格は，歯科で，診察，治療及び処置に用いる場合，患者及び使用者を交差感染から守るために使用する滅菌及び未滅菌の使い捨て形式のビニル手袋(以下，手袋という。)について規定する。

Single-use polyvinyl chloride gloves for dentistry

JIS T 9116:2000 一次性使用的聚氯乙烯检验手套

この規格は，手術を除いた検査，検診，治療行為及び汚染された医療材料を取り扱う場合，患者及び使用者を交差感染から守るために使用する滅菌及び未滅菌の使い拾て形式のピニル手袋(以下，手袋という。)について規定する。またこの規格は，千袋の表面が平滑なもの及び表面の一部又は全面が祖面の予袋にも適用する。

Single-use polyvinyl chloride examination gloves

ASTM F1859-00 无内层的橡胶薄楼板的标准规范

1.1 This specification covers the requirements for the compound and physical characteristics of rubber sheet floor covering without backing. 1.2 The values stated in inch-pound units are to be regarded as the standard. The SI units given in parentheses are for information only. 1.3 The following precautionary statement pertains only to the test method portion, Section 9, 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 limitations prior to use.

Standard Specification for Rubber Sheet Floor Covering Without Backing

ASTM F1860-00 有内层的橡胶薄楼板的标准规范

1.1 This specification covers the requirements for the compound and physical characteristics of rubber sheet floor covering having a rubber wear layer with backing. Products may also contain intermediate layers. 1.2 The values stated in inch-pound units are to be regarded as the standard. The SI units given in parentheses are for information only. 1.3 The following precautionary statement pertains only to the test method portion, Section 9, 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 limitations prior to use.

Standard Specification for Rubber Sheet Floor Covering With Backing

NF D25-250:1999 儿童使用和保育用品.测定合成橡胶或橡胶奶嘴和安抚奶嘴中释放的N-亚硝胺和N-可亚硝化物质的方法

Child use and care articles - Methods for determining the release of N-Nitrosamines and N-Nitrosatable substances from elastomer or rubber teats and soothers.

HG/T 3645-1999 天然橡胶手套中水抽提蛋白质.测定方法.Lowry法

本标准提供了一个测定天然橡胶手套中水溶性蛋白质含量的方法。 本标准也适合于其他橡胶制品中水溶性蛋白质含量的测定。

Method for the determination of aqueous extractable protein in natural rubber gloves using the Lowry method

ASTM D6324-99a 由合成材料生产的阴茎套的标准试验方法

1.1 These test methods shall be used to evaluate male condoms made of various synthetic materials. These test methods also describe the minimum inspection and quality levels that shall be utilized in referee tests. It is not intended to be a routine quality control specification for synthetic condom manufacturing operations. 1.2 These test methods are intended to assist buyers in obtaining synthetic condoms of consistent quality. The safe and proper use of synthetic condoms is excluded from the scope of these test methods. 1.3 The system of units for these test methods is a combination of systems. When the SI units are not utilized, they will be provided in parentheses. 1.4 The annexes in these test methods include important information, such as that on apparatus or materials, that is a mandatory part of these test methods but too detailed for inclusion in the main text. 1.5 The appendixes in these test methods contain information intended to provide guidance.

Standard Test Methods for Male Condoms Made from Synthetic Materials

ARMY MIL-R-46082 B NOTICE 1-1998 厌氧型单成分固持胶

This notice should be filed in front of Mil-R-46082B, dated 10 June 1983.

RETAINING COMPOUNDS, SINGLE COMPONENT, ANAEROBIC

ASTM F1909-98(2004) 预制开口泡沫橡胶桶和桶衬垫规范

1.1 This specification covers preformed open-cell sponge rubber gaskets of the following classes for use in new or reconditioned pails or drums.1.1.1 Class ANon-Oil Resistant.1.1.2 Class BOil Resistant.1.2 The values stated in SI units are to be regarded as the standard.1.3 The following safety hazards caveat pertains only to Section 10, General Test Methods. 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 limitations prior to use.Note 1ISO Equivalency Statement-This proposed specification was found to be not equivalent.

Specification for Preformed Open-Cell Sponge Rubber Pail and Drum Gaskets

ASTM D6355-98(2003) 医用手套人重复损害修补试验的标准试验方法

This RIPT method assesses the potential of skin sensitization with a particular medical product by repeated topical applications to the skin of selected subjects. This is a procedure that has the potential to detect many, but not all, sensitzers. This requires multiple applications to induce a cell-mediated Type IV immune response sufficient to cause an allergic reaction. In general, the sensitization procedure requires 10 multiple 48-h (72-h on weekends) applications of patches containing the study material over a three-week induction phase. Induction is followed by approximately a 21 day rest phase to allow the development of any latent sensitization. Study subjects are then challenged by the application of two consecutive 48-h patches of the study material to naive sites. Responses are evaluated and graded after the removal of each consecutive 48-h patch application. Although this test method is a clinical method, it may be used as part of a risk analysis to determine the potential for Type IV allergic contact dermatitis. This test method assumes that good clinical practices will be utilized, including adequate training of practitioners.1.1 This test method is designed to evaluate the potential of glove materials under test to induce and elicit Type IV skin sensitization reactions (that is, allergic contact dermatitis) in humans.1.2 This test method should be used by individuals experienced in or under the supervision of those experienced in the use of good clinical practice procedures.1.3 During the performance of the Human Repeat Insult Patch Test (RIPT) for determining sensitization, investigators are confronted with skin responses that represent skin irritation (non-immunologic responses) or allergic contact dermatitis (ACD). The numerical scoring system for grading the intensity of both are similar and test facilities may vary in their scores that describe intensities of allergic and irritant skin responses. The hallmark of a mild allergic contact dermatitis is a sustained palpable erythematous reaction. Delayed-type allergic contact reactions from patch tests have intensity characteristics that favor scores of higher values for longer periods of time and typically do not produce a minimal score (score of 1, a just-perceptible erythema) for short durations (less than 48 h). It is the responsibility of the investigator to evaluate the scores in light of irritant reactions so that the responses are allergic in nature and not irritant. The investigator should denote a final score as either due to contact allergy or irritation. Paragraphs 9.5-9.5.5 describe a commonly used scoring system and discuss allergic and irritant responses in detail.1.4 The Draize RIPT was published in 1944 as an attempt to decrease the frequency ACD. The test techniques at that time were just being validated and this experimental design was largely empiric. The principle of the test is as follows:1.4.1 Multiple inductions of the study material at relatively non or low irritancy levels,1.4.2 Approximately a two-week rest period, and1.4.3 A standard diagnostic challenge of approximately 48 h and a delayed reading at approximately 96 h after patch application.1.5 In the intervening years, with further experimentation added to this empiric approach, three additional principles have been learned:1.5.1 Increasing the concentration of the study material,1.5.2 Defining a no effect level (this is possible with only individual ingredients and not the final study material), and 1.5.3 The enhanced sensitivity and the use of occlusion (where occlusion would not ordinarily be present).1.6 In 1945, Henderson and Riley demonstrated that a test panel sample size of 30,000 subjects would have to be employed to ensure statistically that there would be no more than 0.1 % sensitization. If there are no al......

Standard Test Method for Human Repeat Insult Patch Testing of Medical Gloves

ASTM F1909-98 预制开口泡沫橡胶桶和桶衬垫规范

1.1 This specification covers preformed open-cell sponge rubber gaskets of the following classes for use in new or reconditioned pails or drums. 1.1.1 Class A - Non-Oil Resistant. 1.1.2 Class B - Oil Resistant 1.2 the values stated in SI units are to be regarded as the standard. 1.3 The following safety hazards caveat pertains only to the test methods sections of the specification. This standard does not purport to address all of the safety problems, 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 limitations prior to use.

Specification for Preformed Open-Cell Sponge Rubber Pail and Drum Gaskets