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قديم 03-05-2019, 05:44 PM
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قديم 09-28-2021, 06:03 PM   رقم المشاركة : [2]
FrankJScott
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قديم 10-13-2021, 07:45 PM   رقم المشاركة : [3]
FrankJScott
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Part 1-10: Medical Electrical Devices - General Requirements For Safety And Essential Performance - Collateral Standard : Requirements In Order To Develop Closed Circuit Controllers That Are Physiologic En 60601-1-10:2008
For the safety of all medical equipment, it is crucial to have separate information. Standards are not just created to ensure the use of the equipment but also for production. Becoming aware of new standards in medical equipment appliances is as crucial as the general ones. EN 60601-1-10.2008 specifies the specifications for the development (analysis and design), verification and validation of an physiologic closed loop controller. The controller is utilized in a closed loop physiologic control system in medical electronic equipment as well as medical systems to control a specific physiologic parameter. The collateral standard is applicable to all kinds of closed-loop controllers, such as fuzzy, adaptive, and linear. Iteh will be pleased to send you the document mentioned above. See the best clc catalog tc clc-sr-86 information.

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The Calculation And Characterisation Of Bulk Materials EN 17289-2:2020
One component of the same standard may complement the other or regulate entirely different sectors. EN 17178-2: 2020 is the second component of the standard that was previously in use.This document explains how to determine the size-weighted small portion (SWFF) and size-weighted small portion of crystallized silicona (SWFFCS). It also lists the preconditions and assumptions to be fulfilled to allow this method to be valid.This document will allow users to judge bulk materials based on their fine fragment size as well as crystalline silica contents.Annexe A provides a precise method to evaluate the SWFFs of bulk materials diatomaceous. An Annex A provides specific guidelines for evaluating SWFF of diatomaceous Earth bulk materials. This is because of the porosity inside.This document covers crystalline silica containing bulk material which has been thoroughly studied and validated for the assessment of the size-weighted, fine fraction and the crystallized silica.It is possible to get a better idea of the importance of these standards through comparing the technical parameters of the production standard with those of individual standards. If you have questions regarding the application, you can always reach out to the experts in international standards. See the recommended iec catalog standards iec-60793-1-49-2018 site.

Woodworking Machines – Safety – Part 10 Building Site Saws As Well As Contractor Saws (Iso 19085-8 / 2018 Updated Version For 2019-12). EN ISO 19085-10:2019/A11:2020
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Health Informatics: Device Interoperability – Part 10201: Point-Of-Care Medical Device Communication – Domain Information Model (Iso/Ieee 11073/10201:2020). EN ISO/IEEE 11073-10201:2020
Documents pertaining to medical devices may contain many different parts. They can complement one other, and may discuss entirely different technologies. An example of this is EN ISO /IEEE 11073-10201: 2020.This project's goal is to create a general data model, based on object-oriented concepts, which can be used to detect and categorize medical device communications at the point-of-care (POC). This project focuses primarily on medical devices utilized in acute care, and the transmission of vital patient information.Since information technology is increasingly utilized in expanding businesses and improving productivity, we suggest you consider purchasing documents that will standardize their use on a global scale. See the top rated iso catalog tc iso-iec-jtc-1-sc-27-wg-2 review.



FrankJScott غير متواجد حالياً   رد مع اقتباس
قديم 02-15-2022, 03:54 PM   رقم المشاركة : [4]
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FrankJScott
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قديم 12-01-2023, 08:36 PM   رقم المشاركة : [6]
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