天然胶乳医用手套检测

发布时间：2024-06-21 作者：中析研究所浏览：

GB/T 9881-2008橡胶.术语

本标准定义了橡胶工业所使用的术语。本标准不对预定用于特殊橡胶制品的术语进行定义，对于这些术语，请参见参考文献所列标准。本标准不适用于特殊橡胶制品的术语和定义。有些术语在其定义前加有带括号的说明，以表明该术语专门限用于某一具体领域，例如“<胶乳>”。当某一术语有一个或多个同义词时，这些术语的同义词列于优选术语之后。除非另有说明，所有术语均为名词。

GB/T 9887-2008胶乳制品术语

本标准规定了胶乳制品主要技术用语及其定义。本标准适用于胶乳制品制修订标准及编写技术文件、书刊时使用。

GB/T 21870-2008天然胶乳医用手套水抽提蛋白质的测定.改进Lowry法

警告——本标准使用者应熟悉一般实验室操作。本标准不涉及任何安全性问题，即使是与它有关的也不例外，使用者应建立相应的安全和健康规范，并使之符合的规定。1 范围本标准规定了天然胶乳医用手套水抽提蛋白质含量的测定，也适用于其他天然胶乳制品中水抽提蛋白质含量的测定，但抽提过程和次数没有得到证实，会随试验样品类型不同而变化。附录C介绍了医用手套中几种特种蛋白质的其他测定方法，但不具有通用性。本标准仅涉及分析方法，与取样无关，也不涉及测定结果的安全性或标志要求。

GB 24788-2009医用手套表面残余粉末、水抽提蛋白质限量

本标准规定了医用手套表面残余粉末、水抽提蛋白质的限量。本标准适用于一次性使用医用橡胶手套、一次性使用灭菌橡胶外科手套、一次性使用医用丁腈橡胶检查手套、一次性使用聚氯乙烯医用检查手套和一次性使用非灭菌橡胶外科手套。

YY/T 0616.3-2018一次性使用医用手套第3部分:用仓贮中的成品手套确定实际时间失效日期的方法

YY/T 0616的本部分规定了用以确定在其终包装中、贮存在典型仓贮条件下的医用手套的货架寿命的研究设计。本部分适用于所有由合成或天然乳胶制成的外科和检查手套。

HG/T 5056-2016GB 7544在天然橡胶胶乳避孕套质量管理中的使用指南

本标准是GB 7544的使用指南，规定了避孕套在开发、生产、质量认证以及采购时涉及的质量问题。本标准以避孕套在设计、生产以及流通环节的质量管理体系为中心，强调避孕套的性能、安全和可靠性。

ISO 12243-2003医用天然胶乳手套.用改良的半细胞法测定水可萃取蛋白质

This International Standard specifies a method for the determination of the amount of water-extractable protein in natural rubber (NR) gloves for medical use. The method is potentially suitable for the determination of extractable protein in other articles made from NR latex; however the extraction procedures and times have not been validated and will vary with the type of article to be tested. Other methods for the determination of specific proteins in medical gloves exist (see Annex C) but they are not of general applicability.nThis International Standard is concerned solely with the method of assay. It is not concerned with sampling nor does it purport to address the safety implications of the values obtained or requirements for labelling.

GSO ISO 12243-2017天然胶乳制医用手套用改良Lowry法测定水溶性蛋白质

This International Standard specifies a method for the determination of the amount of water-extractable protein in natural rubber (NR) gloves for medical use. The method is potentially suitable for the determination of extractable protein in other articles made from NR latex; however the extraction procedures and times have not been validated and will vary with the type of article to be tested. Other methods for the determination of specific proteins in medical gloves exist (see Annex C) but they are not of general applicability. This International Standard is concerned solely with the method of assay. It is not concerned with sampling nor does it purport to address the safety implications of the values obtained or requirements for labelling.

DIN EN 455-4-2009一次性医用手套.第4部分:货架寿命测定的要求和试验,德文版本EN 455-4:2009

This part of EN 455 specifies requirements for shelf life for medical gloves for single use. It also specifies therequirements for labelling and the disclosure of information relevant to the test methods used.This European Standard applies to existing, new and significantly changed designs. Existing designs that do notcurrently have ageing data available should generate that data within a reasonable period of time.This European Standard does not specify the size of a lot. Attention is drawn to the difficulties that can be associatedwith the distribution and control of very large lots. The recommended maximum individual lot size for production is500 000.