What is EN 60793-1-40:2016 ?

Title: Understanding EN 60793-1-40:2016 and EN 60601-1-2:2016

Introduction:

Optical fibers and cables are essential components in a wide range of industries, including telecommunications, healthcare, and data processing. These components undergo rigorous testing to ensure their performance and quality. Two key international standards that play a crucial role in ensuring the safety and performance of optical fibers and cables are EN 60793-1-40:2016 and EN 60601-1-2:201In this article, we will provide an overview of these two standards and their purpose.

EN 60793-1-40:2016: The Basics

EN 60793-1-40:2016 is a professional technical standard that outlines the guidelines and requirements for the characterization of optical fiber categories and the measurement methods and test procedures to be used. It provides a common language for manufacturers and users to discuss and specify optical fibers.

The standard defines 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, manufacturers and users can have a clear understanding of the properties they are dealing with, which is essential for selecting the right product for a specific application.

Measurement Methods and Test Procedures:

EN 60793-1-40:2016 provides guidelines for the measurement of various properties of optical fibers, such as attenuation, bending loss, and mechanical strength. The standard also outlines the test procedures that should be used to verify the properties of optical fibers. These tests are designed to measure the performance of the optical fibers in various applications, such as high-speed data transmission and fiber optic communications.

EN 60601-1-2:2016: The Ensuring Safety and Performance of Equipment

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 this standard 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 60601-1-2:2016:

EN 60601-1-2:2016 provides several key requirements that medical electrical equipment must meet. These requirements include:

Electrical safety: Equipment must be designed and manufactured to minimize the risk of electrical shock or other injuries.

EMC: Equipment must be designed to minimize the risk of electromagnetic interference (EMI) and maximize the rejection of EMI from other sources.

Performance: Equipment must perform as specified in the relevant regulations and standards.

Test: Equipment must undergo testing to verify that it meets the requirements of the standard and is safe for use in healthcare environments.

Conclusion:

EN 60793-1-40:2016 and EN 60601-1-2:2016 are two crucial international standards that play a critical role in ensuring the safety and performance of optical fibers and cables, as well as medical electrical equipment. By establishing these standards and requirements, manufacturers and users can have a clear understanding of the properties and characteristics of the products they are dealing with, which is essential for selecting the right product for a specific application.