What is BS EN ISO 13732-3:2015 ?

What is BS EN ISO 13732-3:2015?

BS EN ISO 13732-3:2015 is a document published by the British Standards Institution (BSI) that outlines the requirements for explosion-resistant electrical equipment. The standard is part of the BS 8599 series of standards, which provide guidelines for the design, manufacture, and testing of electrical equipment.

What is the purpose of BS EN ISO 13732-3:2015?

The main purpose of BS EN ISO 13732-3:2015 is to provide guidelines for the design, manufacture, and testing of electrical equipment that is intended to operate in explosive hazardous areas. By adhering to the requirements outlined in the standard, manufacturers can ensure that their products are safe, reliable, and suitable for use in such environments.

Key Aspects of BS EN ISO 13732-3:2015

BS EN ISO 13732-3:2015 has several key aspects that manufacturers must adhere to in order to ensure the safety and reliability of their electrical equipment. These key aspects include:

Electrical Performance: The standard outlines the requirements for the electrical performance of the equipment, including the maximum allowable voltage, current, and power consumption.

Explosion-Resistance: The standard requires that electrical equipment be designed and manufactured to withstand an explosion that is capable of damaging or destroying the equipment.

Electrical Circuit: The standard specifies the requirements for the electrical circuit, including the use of insulated wires, fuses, and circuit breakers.

marking and documentation: The standard requires manufacturers to clearly mark and document their electrical equipment, including the maximum allowable voltage, current, and power consumption.

to EN ISO 13485:2015

EN ISO 13485:2015 is an internationally recognized standard that outlines the requirements for a quality management system specifically designed for medical devices. The standard is designed to ensure that medical devices meet customer and regulatory requirements, and is based on the ISO 13485:2015 standard.

Key Requirements of EN ISO 13485:2015

EN ISO 13485:2015 has several key requirements that manufacturers must adhere to in order to ensure the safety and reliability of their medical devices. These key requirements include:

Quality Management System: The standard requires that organizations have a quality management system in place that is designed to ensure continuous improvement and compliance with the requirements of the standard.

Documentation: The standard requires manufacturers to maintain accurate and up-to-date records of their medical devices, including information about the design, manufacturing, and testing of the devices.

Testing: The standard requires manufacturers to test their medical devices to ensure that they meet the requirements of the standard and are safe for use.

Traceability: The standard requires manufacturers to be able to trace their medical devices from the point of origin to the point of use, in order to ensure that they are properly maintained and updated.

In conclusion, EN ISO 13732-3:2015 and EN ISO 13485:2015 are both important standards that manufacturers must adhere to in order to ensure the safety and reliability of their electrical equipment. By following the guidelines and requirements outlined in these standards, manufacturers can ensure that their products are safe for use in explosive hazardous areas and meet the requirements of customers and regulatory bodies.