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匿名  發表於 2021-10-14 00:58:53

ISO Standardization Is Key For Business Growth

Part 1: Safety Requirements And The Essential Performance Of Medical Electrical Equipment. Collateral Standard - Electromagnetic Disturbances. Tests And Specifications En 60601-1-2:2015
The specification of medical equipment requires more precise and specific knowledge. Each type of medical device has their own set of specifications. This document covers the essential security and performance of medical Equipment (ME), equipment and ME systems in the face of electromagnetic disturbances and electromagnetic disturbances that emanate from medical equipment and systems. The requirements for safety of medical equipment usage in the first section of the standard. See the top rated iso catalog standards iso-15394-2000 blog.

International Standardizations Should Consider Innovative Technologies
Innovative technologies are taking over the globe. Every second and every minute, each day, a new device and a brand new method of using existing technologies are invented. This is transforming the world. Human health is affected by the proliferation of electronic devices and communications and artificial intelligence. It is possible for humanity to suffer from the inability to maintain the proper functioning of these devices. The speed at which the Internet can transfer data transmission has led to an increase in the risk of leakage of information. This is why the issue of security becomes more pressing every day. We will provide you with international standards for safe data transmission, and technical recommendations regarding how these technologies can be used. Check out the top rated clc catalog standards clc-tr-50459-7-2007 information.

Characterization Of Bulk Materials: Determination Of A Size-Weighted Fine Fraction And Crystal Silica Content - Part 1: General Information And Choice Of Testing Methods EN 17289-1:2020
Regulations can be complicated locally as well as globally due to the vast variety of production materials. International standards are being created to ease the process for companies and organizations that want to access new markets.This document defines the specifications and testing methods for the determination of the size-weighted fraction (SWFF) and the size-weighted fine fraction (SWFFCS) of silica crystalline (SWFFCS) in bulk materials.This document offers guidelines on how to prepare the sample and identify the crystalline silica by X-ray powder difffractometry (XRD), Fourier Transform Infrared Spectroscopy, (FTIR).EN 1789-2 is the method of formulating the size-weighted fine fraction based on the measurement of the range of particle sizes. This assumes that the distribution of silica crystals particles in bulk material is the same. EN 17289-3 describes a liquid sedimentation method for determining the fine size-weighted portion of crystallized silica. Both methods are subject to limitations and assumptions. These limitations are explained in EN 17289-2, EN 17289-3. If properly validated it is possible that the EN 17289-3 methodology can be applied to other constituents.This document may be used to evaluate bulk crystalline silica material, provided it has been thoroughly researched and verified to permit the assessment of size-weighted, fine fragments as well as crystalline silica.The existence of the technology documentation base will assist to scale up production when your industry is directly connected to the information contained in this document. For more details, you can follow the link to our site. Check out the top rated 36c34b0762494375907aafef2fa89d9e samples 23916 information.

Machine Tools Safety – Safety For Presses - Part 4 : The Safety Requirements Of Pneumatic Presses. (Iso 16092-4.2019). EN ISO 16092-4:2020
Safety concerns are always at the top of any regulatory framework.This document, along with ISO 16092-2, provides technical safety standards that must be met by everyone who is accountable for the development, production, and delivery of pneumatic presses specifically designed to operate with cold metals, or other materials that are primarily made from cold steel.This document will cover all dangers associated with pneumatic presses. They are intended to be used in conditions that are reasonable foreseeable by the manufacturer. All of these phases are described in ISO 12100 :2010, Section 5.4.If you're interested, click the link on our site to access the full technical specifications. Contact the team for any clarifications. Check out the top iec catalog standards iec-ts-62257-7 information.

Health Informatics - Device Interoperability Part 10201 Point-Of Care Device Communication - Domain Information Model (Iso/Ieee 11073/10201:2020 EN ISO/IEEE 11073-10201:2020
Like any other standard, documents pertaining to the use of devices within medical practice have distinct parts that could be a complement and also talk about completely different technology. One example is EN ISO / IEEE 11073-10201: 2020.The scope of this project is to establish a general object-oriented information model that may be used to structure information and define services that are used in point-of-care (POC) medical device communications. The focus is on acute care medical devices as well as the communication of vital signs and information.Since information technology is increasingly used in expanding businesses and improving productivity, we suggest you consider purchasing documents that will standardize their use internationally. See the most popular cen catalog standards en-15890-2010 blog.

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匿名  發表於 2021-10-14 21:04:20
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匿名  發表於 2021-10-26 08:46:16

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匿名  發表於 2021-10-27 06:00:11
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匿名  發表於 2021-10-27 07:04:08

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