手術服和手術簾檢測

手術服和手術簾檢測項目報價？??解決方案？??檢測周期？??樣品要求？

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DB31/T 930-2015非織造產品(醫衛、清潔、個人防護、保健)碳排放計算方法

本標準規定了非織造產品（醫衛、清潔、個人防護、保健)術語和定義，碳排放計算的邊界、數據獲取的方法、計算方法，產品碳排放的外包裝標識。本標準適用于非織造產品（醫衛、清潔、個人防護、保健)企業生產過程中碳排放的計算。本標準所指溫室氣體排放僅指二氧化碳排放。

DIN EN 13795-1-2019手術服和手術簾. 要求和試驗方法. 第1部分: 手術簾和手術服; 德文版 EN 13795-1-2019

This European Standard specifies information to be supplied to users and third party verifiers in addition to the usual labelling of medical devices (see EN 1041 and EN ISO 15223-1), concerning manufacturing and processing requirements. This European Standard gives information on the characteristics of single-use and reusable surgical gowns and surgical drapes used as medical devices for patients, clinical staff and equipment, intended to prevent the transmission of infective agents between clinical staff and patients during surgical and other invasive procedures. This European Standard specifies test methods for evaluating the identified characteristics of surgical drapes and gowns and sets performance requirements for these products.

DIN EN 13795-2-2019手術服和手術簾. 要求和試驗方法. 第2部分: 潔凈服; 德文版 EN 13795-2-2019

This European Standard specifies information to be supplied to users and third party verifiers in addition to the usual labelling of medical devices (see EN 1041 and EN ISO 15223-1), concerning manufacturing and processing requirements. This European Standard gives information on the characteristics of single-use and reusable clean air suits used as medical devices for clinical staff, intended to prevent the transmission of infective agents between clinical staff and patients during surgical and other invasive procedures. This European Standard specifies test methods for evaluating the identified characteristics of clean air suits and sets performance requirements for these products.

DIN EN ISO 11810-2016激光和相關的激光設備.手術單和/或病患者護罩耐激光性的試驗方法和分類.初級點燃, 穿透, 火焰蔓延和次級點燃

This International Standard applies to disposable and reusable, as well as woven and non-woven materials used as surgical drapes and other patient protective covers which claim to be laser resistant. The purpose of this standard is to provide a standardized method for testing and classifying surgical drapes and other patient protective covers with respect to laser-induced hazards. It also covers the issue of laser-induced secondary ignition. An appropriate classification system is given. It is not the purpose of this standard to serve as a general fire safety specification, and as such, this standard does not cover other sources of ignition. All materials reflect portions of the beam and it is necessary for the user to decide whether specular reflectance may be a hazard. This measurement, however, is not covered in this standard. The results of this part of ISO 11810 are not to be applied to other wavelengths and temporal formats. The 20 W CO2 laser (continuous wave) has been selected as the laser to be used for ISO 11810. Users of products tested by this method are cautioned that the laser resistance of a surgical drape and/or patient protective cover will be wavelength sensitive and that a surgical drape and/or patient protective cover are better tested at the wavelength for which it is intended to be used. If tested using other wavelengths, the power settings and modes of delivery need to be explicitly stated.