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手术服和手术帘检测

发布日期: 2024-06-21 17:34:53 - 更新时间:2024年06月29日 15:22

手术服和手术帘检测项目报价?  解决方案?  检测周期?  样品要求?

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DB31/T 930-2015非织造产品(医卫、清洁、个人防护、保健)碳排放计算方法

本标准规定了非织造产品(医卫、清洁、个人防护、保健)术语和定义,碳排放计算的边界、数据获取的方法、计算方法,产品碳排放的外包装标识。本标准适用于非织造产品(医卫、清洁、个人防护、保健)企业生产过程中碳排放的计算。本标准所指温室气体排放仅指二氧化碳排放。

DIN EN 13795-1-2019手术服和手术帘. 要求和试验方法. 第1部分: 手术帘和手术服; 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手术服和手术帘. 要求和试验方法. 第2部分: 洁净服; 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激光和相关的激光设备.手术单和/或病患者护罩耐激光性的试验方法和分类.初级点燃, 穿透, 火焰蔓延和次级点燃

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.

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