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发表于 2021-10-13 22:45:52 | 显示全部楼层

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Part 1-11: Basic Safety And Essential Performance Requirements For Medical Electrical Equipment. Collateral Standard: Requirements Concerning Medical Electrical Equipment And Equipment Used In The Home Healthcare Environment. En 60601-1-11: 2015
Healthcare at home is increasing in popularity of demand with each day. It is developing more standards. This International Standard covers basic safety and the essential performance of medical electrical equipment for use in the health care setting at home. The International Standard applies regardless of whether the equipment or system is intended to be used by a lay person or by trained healthcare professionals. It describes in detail the techniques used to meet all security requirements. This is the reason we're stressing the crucial necessity of having a regular awareness even for equipment used at home. Follow this link to stay up-to-date with the latest information by following our website. Check out the most popular cen catalog standards en-12649-2008-fpra1 blog.

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When it comes to the process of manufacturing as well as the utilization of different materials, an array of methods are applied. Each of them requires a certain level of regulation, depending on the magnitude of the task. EN 17289-3 is the year 2020. It defines the method for applying the crystalline silica.This document specifies the method of determining the size-weighted fine fraction (SWFF) and the size-weighted fine fraction of silica crystalline (SWFFCS) in bulk materials, using the sedimentation technique using a liquid sedimentation technique.This document will enable the users to examine bulk materials with respect to their size weighted fine fraction as well as crystal silica content.This document covers the crystalline silica that contains bulk material which has been thoroughly studied and validated for the assessment of the size-weighted, fine fraction as well as the crystalline silica.Specification of production methods simplifies the process for building an effective control system. If you're interested in expanding into new markets, we strongly recommend that you look into buying international standards for your plant. See the recommended cen catalog standards en-15166-2008 site.

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As new methods of technology and air pollution are developed as new technologies and air pollutions become more prevalent, environmental and safety concerns evolve. One document that offers a solution to this problem is EN 16524: 2020.This document outlines a strategy for reducing environmental impact through design and development of products. It is specific to mechanical products as described in 3.1.This approach can be utilized to design new products, but it could be used for the creation of new products if the relevant assumptions are made regarding the reference product. This approach is aimed at companies that have chosen to incorporate an ecodesign approach to optimise environmental impacts within the duration of the lifecycle of the product with respect to other factors of the product such as functionality, quality, costs, etc.It meets a few of the specifications in ISO 14001 :2015 regarding the incorporation of environmental aspects into the design of products. This document is intended for those who directly participate in the design and production of mechanical goods. The methodology proposed is designed to start ecodesign initiatives in businesses in a learning and continuous improvement approach.A template is also included in this document, which companies can use to communicate their environmental strategy. This document does not allow for the comparability of products, even ones that have similar characteristics, from different suppliers. The document isn't appropriate for certification of products.This document is crucial in the 21st century. This is why you must be looking into the document and incorporating it into your organization's activities. See the top rated clc catalog standards en-61926-1-2000 site.

Health Informatics -- Requirements For International Machine-Readable Code Of Medical Package Identifiers For Products ISO/TS 16791:2014 NEW version ISO/TS 16791:2020
As new technologies emerge as new technologies are developed, there will be a variety of rules that govern their use and minimize risk. One example of such documents that are able to changing due to the rapid development of new technologies and technology is EN ISO / IEEE 11073-10201: 2020.This document provides guidelines on the identification and labeling of medicinal products starting from the point of production of the packaged product until the point of dispensing the product. This document outlines best practices in AIDC barcoding solutions. It is also possible to think about interoperability requirements for other AIDC technologies, for instance RFID. Radio Frequency IdentificationIf you've employed a previous version of this document and continue to work within the same area of operation We strongly suggest purchasing this document, which has updated recommendations and international guidelines. Check out the top cen catalog standards cen-ts-15810-2008 review.

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