Part 2-8 Part 2-8: Safety And Performance Specifications For Electrical Equipment Used In Medical Facilities En 60601-2-8:2015
Narrowly specified norms and documents sometimes are neglected with companies due to a variety of reasons. The reason could be that standards are continuously changing. EN 60601-2-8.2015 is an important document for businesses dealing with medical equipment. It specifies specific safety requirements and essential performance requirements for therapeutic X-ray equipment with nominal X-ray tube voltages of the 10 kV range up to 1 MV when hooked to mains of supply alternating current. It addresses the safety requirements in terms of precision and reproducibility. This new edition cancels the IEC 60601-2-8 1st edition and replaces it. This edition is a technological revise that brings the standard into line with IEC 60601-1-3 as well as its other guidelines. We strongly suggest following the hyperlink to the site for your company if you operate in the field of mentioned equipment. Have a look at the top
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Innovative Technologies As A Theme To International Standardizations
Innovative technologies are taking over the globe. Everyday, every second, a brand new device, or a new approach to applying existing technology, is created. The world is undoubtedly changing due to this. Because of the impact of electrical devices and artificial intelligence on our lives, maintaining these devices in chaos could result in devastating consequences for humanity. Also, one should not overlook the fact that with the development of the Internet and the acceleration of methods for transferring information the amount of risk of information leakage has increased and the issue of security is becoming more and more relevant every day. Today, we'll provide information on the technical aspects of where and how to use these technologies, as well as the international standards that are responsible for data security. Check out the best
cen catalog standards en-17333-2-2020 review.
Characterization Of Bulk Materials - Determination Of A Size-Weighted Fine Fraction And The Content Of Crystalline Silica - Part 1 General Information And Selection Of Test Procedures EN 17289-1:2020
The wide range of materials used in production complicates regulation both locally, and globally. International standards have been created to aid companies and organizations entering new markets. One of these is EN 17289-1:2020.This document describes the requirements for the calculation of the size-weighted fine fraction (SWFF) and the size weighted fine fragment crystalline silica (SWFFCS).This document includes guidance on preparation and determination through Fourier Transform Infrared Spectroscopy and X-ray Pulsed Diffractometry.EN 1789-2 provides a method to calculate the size-weighted fine percent by measuring the size of particles distribution. The method assumes, however that the sizes of the crystalline particles are similar to the bulk material. EN 1789-3 describes a fluid sedimentation technique to calculate the size-weighted fine fraction of crystalline silica. Both methods are governed by the assumptions and limitations. If tested and validated it is possible that the EN 17289-3 methodology could be applied to different constituents.This document can be used to describe the bulk materials containing crystalline silicona that have been fully examined and verified to evaluate the size-weighted fine fraction, as well as crystalsilica.If your business comes into contact the material in the description, then it will be a great opportunity to increase production. Click here to visit our website for more details. See the most popular
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Machine Tools Safety Presses Part 4: Safety Requirements To Pneumatic Presses (Iso 160922-4.2019) EN ISO 16092-4:2020
Safety issues are usually the first in creating a regulatory system for a manufacturing or business, which is the reason there are many of international standards that address this topic, one of which is EN ISO 16092-4:2020.This document, along with ISO 16092-2, describes the technical safety standards which must be adhered to by anyone who is accountable for the design, development, and delivery of pneumatic presses specifically designed to work with cold metals or materials made up of cold steel.This document addresses all hazards that can affect pneumatic presses if they are employed in line to their intended usage and under conditions of misuse which are reasonably predicted by the manufacturer (see Clause 4.) Each phase of the lifetime of the machinery as described in ISO 12100:2010, 5.4, have been taken into account.If you're interested in purchasing this document, please click on the link to see all technical specifications. Contact the team that will clarify all details. See the most popular
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Health Informatics - Device Interoperability Part . 20701 Communication At The Point Of Care With Medical Devices . Medical Device Exchange With A Service-Oriented Technology (Iso/Ieee 11073-20701:2020). EN ISO 11073-20701:2020
Communications technologies are utilized in many areas including those that are directly related to this field as well as in medical fields. The introduction of various medical devices require a intricate transformation. To make these processes easier, international documents have been developed.
This standard addresses a service-oriented medical device design and communication protocol specification. It is applicable to distributed system of PoC (Point-of-Care) medical devices as well as medical IT systems that require data exchange as well as safe control over PoC medical devices. It defines the functional components as well as the communication relations and binding to protocols specifications.This document is specialized and narrowly defined. We recommend to learn more about its technical parameters and consult managers who are experts in the international selection of documents. Check out the best
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