Title: Understanding EN 60598-1: 2016 and EN 60601-1-2: 2016
Optical fibers and cables are widely used in various industries due to their numerous benefits. These materials have unique physical properties that determine their performance characteristics, such as attenuation, bending radius, and mechanical strength. In order to ensure the quality and performance of these products, manufacturers must follow a series of guidelines and standards. Two of these standards are EN 60598-1: 2016 and EN 60601-1-2: 201In this article, we will discuss the purpose and requirements of these two standards.
EN 60598-1: 2016: The Basics
EN 60598-1: 2016, also known as ISO 15593-1: 2016, is a professional technical standard that outlines the requirements for the characterization of optical fiber categories and the measurement methods and test procedures to be used. This standard provides a common language for manufacturers and users to discuss and specify optical fibers.
The primary purpose of EN 60598-1: 2016 is to define different categories of optical fibers based on their characteristics and performance. These categories include parameters such as attenuation, geometry, mechanical properties, and environmental properties. By establishing these categories, the standard enables manufacturers and users to have a common understanding of the properties and characteristics of optical fibers, which is essential for selecting the right product for a specific application.
Measurement Methods and Test Procedures:
EN 60598-1: 2016 provides guidelines for the measurement of various parameters of optical fibers, such as attenuation, bending radius, and mechanical properties. The standard also specifies the test procedures that manufacturers must follow to verify the conformity and performance of their products.
EN 60601-1-2: 2016: The Similarities
EN 60601-1-2: 2016, also known as IEC 60601-1-2, is an international standard for medical electrical equipment. It provides requirements and guidelines for the basic safety and essential performance of equipment used in healthcare facilities, such as hospitals and clinics.
The primary aim of EN 60601-1-2: 2016 is to ensure that medical electrical equipment does not interfere with other devices and systems, and is immune to electromagnetic disturbances. With the increasing reliance on electronic systems and wireless technologies in healthcare, it is crucial to establish safety measures to prevent conflicts or disruptions in medical environments.
Key Requirements of EN 60598-1: 2016 and EN 60601-1-2: 2016:
Both EN 60598-1: 2016 and EN 60601-1-2: 2016 have key requirements that manufacturers must follow to ensure the quality and performance of their products. These requirements include:
The products must be designed and manufactured to meet the requirements specified in Table 1 of the standard.
The products must be tested in accordance with the procedures specified in Table 2 of the standard.
The products must be labeled in accordance with the requirements specified in Table 3 of the standard.
The products must be accompanied by a user manual that includes information about the product's capabilities, limitations, and proper usage.
The products must be designed and manufactured to meet the specific needs of their intended application, and must be tested to ensure they perform as expected in their specific environment.
Conclusion:
EN 60598-1: 2016 and EN 60601-1-2: 2016 are essential standards for ensuring the quality and performance of optical fibers and medical electrical equipment.
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