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dackjicko:
ผมได้สม้คร Google Custom Search ไปแล้วดันได้สคลิปแบบนี้มา


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smf 2.0.14 จะเอาไปวางที่ไหนถึงจะใช้งานได้ครับนี่

FrankJScott:
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Part 2 Part 2: Safety And Performance Specifications For Medical Electrical Equipment En 60601-2-3:2015
The medical industry is increasingly utilizing short-wave therapy. It is the reason its regulation has gained significant importance. IEC 60601-2-3.2012 defines the fundamental safety and essential performance requirements of equipment used for therapeutic use in short waves. Medical equipment that employs short-wave radiation therapy to treat patients is defined as equipment that exposes them to magnetic or electric fields that have frequencies higher than 13MHz, but less than 45MHz. Iteh can be contacted for more details about the document, given that it is of a very narrow scope. Have a look at the top sist catalog standards sist-en-iso-15874-2-2013 info.
 
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Many methods are used to create and utilize different materials. Each method requires a specific amount of regulation, based on the magnitude of the undertaking. EN 17178-3, 2020 is the document that defines the exact procedure for the use of crystallized silicona.This document explains how to determine the fine fraction that is size-weighted and crystalline (SWFF), and the size-weighted fine portion (SWFFCS), for bulk materials by using an approach to sedimentation that employs the method of liquid sedimentation.This document aims to facilitate people to judge bulk materials according to their size-weighted crystalline silica and fine fraction.This document applies to the bulk silica and crystals that have been thoroughly evaluated and confirmed for the evaluation and weighted size of the fine fraction.The specification of manufacturing methods allows you to build a control network. If you're planning to increase your market reach, we recommend you purchase international standards for your business. Have a look at the top rated cen catalog standards en-3056-1994 review.
 
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Health Informatics -- Requirements For International Machine-Readable Coding Of The Identifiers On Packages Of Medicines. ISO/TS 16791:2014 NEW version ISO/TS 16791:2020
As new technologies develop, there will be more regulations to govern their use, and limit the risks. EN ISO 11073/10201 IEEE - 2020 is one illustration.This document gives guidance on the identification and labelling of medical products from the time of manufacturing of the product to the point at which the product can be disposed of. This document provides guidelines for AIDC barcoding solutions. However, users may also be interested in interoperability requirements for different AIDC methods, e.g. Radio Frequency IdentificationIf you've previously worked with this document and are still operating in the same industry, we recommend buying this new version with updated recommendations. See the recommended clc catalog standards en-50181-2010 review.
 

mahi01:
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