歡迎訪問中科光析科學技術研究所官網(wǎng)!

免費咨詢熱線
400-640-9567|
天然膠乳醫(yī)用手套檢測項目報價???解決方案???檢測周期???樣品要求? |
點 擊 解 答??![]() |
本標準定義了橡膠工業(yè)所使用的術語。本標準不對預定用于特殊橡膠制品的術語進行定義,對于這些術語,請參見參考文獻所列標準。本標準不適用于特殊橡膠制品的術語和定義。有些術語在其定義前加有帶括號的說明,以表明該術語專門限用于某一具體領域,例如“<膠乳>”。當某一術語有一個或多個同義詞時,這些術語的同義詞列于優(yōu)選術語之后。除非另有說明,所有術語均為名詞。
本標準規(guī)定了膠乳制品主要技術用語及其定義。本標準適用于膠乳制品制修訂標準及編寫技術文件、書刊時使用。
警告——本標準使用者應熟悉一般實驗室操作。本標準不涉及任何安全性問題,即使是與它有關的也不例外,使用者應建立相應的安全和健康規(guī)范,并使之符合的規(guī)定。1 范圍 本標準規(guī)定了天然膠乳醫(yī)用手套水抽提蛋白質含量的測定,也適用于其他天然膠乳制品中水抽提蛋白質含量的測定,但抽提過程和次數(shù)沒有得到證實,會隨試驗樣品類型不同而變化。附錄C介紹了醫(yī)用手套中幾種特種蛋白質的其他測定方法,但不具有通用性。 本標準僅涉及分析方法,與取樣無關,也不涉及測定結果的安全性或標志要求。
本標準規(guī)定了醫(yī)用手套表面殘余粉末、水抽提蛋白質的限量。本標準適用于一次性使用醫(yī)用橡膠手套、一次性使用滅菌橡膠外科手套、一次性使用醫(yī)用丁腈橡膠檢查手套、一次性使用聚氯乙烯醫(yī)用檢查手套和一次性使用非滅菌橡膠外科手套。
YY/T 0616的本部分規(guī)定了用以確定在其終包裝中、貯存在典型倉貯條件下的醫(yī)用手套的貨架壽命的研究設計。本部分適用于所有由合成或天然乳膠制成的外科和檢查手套。
本標準是GB 7544的使用指南,規(guī)定了避孕套在開發(fā)、生產(chǎn)、質量認證以及采購時涉及的質量問題。本標準以避孕套在設計、生產(chǎn)以及流通環(huán)節(jié)的質量管理體系為中心,強調避孕套的性能、安全和可靠性。
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.
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.
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.
前沿科學
微信公眾號
中析研究所
抖音
中析研究所
微信公眾號
中析研究所
快手
中析研究所
微視頻
中析研究所
小紅書