Road vehicles — Environmental conditions and testing for electrical and electronic equipment — Part ...
This document applies to electric and electronic systems and components for vehicles including electric propulsion systems and components with maximum working voltages according to voltage class B. It describes the potential environmental stresses and specifies tests and requirements for the specific mounting location on/in the vehicle.
This document contains the terminology for the ISO 16750…
Scope
This National Standard of Canada applies to four types of middle distillate fuel oils that are suitable for use in liquid
fuel burning equipment without preheating [types 0, 1, 2 and 2(B6-B20)], and three types of fuel oils that contain
residual fuel components that require preheating (types 4, 5 and 6).
The heating fuel oils covered by this standard are intended for use in oil burning…
Accuracy (trueness and precision) of measurement methods and results — Part 3: Intermediate precisio...
This document provides
a) a discussion of alternative experimental designs for the determination of trueness and precision measures including reproducibility, repeatability and selected measures of intermediate precision of a standard measurement method, including a review of the circumstances in which their use is necessary or beneficial, and guidance as to the interpretation and application…
Empty enclosures for low-voltage switchgear and controlgear assemblies - General requirements
IEC 62208:2023 CMV contains both the official standard and its commented version. The commented version provides you with a quick and easy way to compare all the changes between IEC 62208:2023 edition 3.0 and the previous IEC 62208:2011 edition 2.0. Furthermore, comments from IEC SC 121B experts are provided to explain the reasons of the most relevant changes, or to clarify any part of the…
Empty enclosures for low-voltage switchgear and controlgear assemblies - General requirements
IEC 62208:2023 applies to empty enclosures, as provided by the enclosure manufacturer, prior to the incorporation of switchgear and controlgear components by the assembly manufacturer. This document specifies general definitions, classifications, characteristics and test requirements of enclosures to be used as part of switchgear and controlgear assemblies (e.g. in accordance with the product…
Standard Method for Testing and Assessing Particle and Chemical Emissions from 3D Printers
Scope
1.1 This standard presents methodologies for characterizing and quantifying coarse, fine, and ultrafine
particles and volatile organic compound (VOC) emissions from operating three-dimensional (3D) printers
under normal conditions of use in defined indoor environments including classroom, office, and residential
scenarios.
1.2 This method primarily applies to the emissions of particles…
Guidance for use of radiation-sensitive indicators
This document covers procedures for using radiationsensitive indicators (referred to hereafter as indicators) in radiation processing. These indicators may be labels, papers, inks or packaging materials which undergo a visual change when exposed to ionizing radiation (1-5).
The purpose for using indicators is to determine visually whether or not a product has been irradiated, rather than to…
Ships and marine technology — Procedure for testing the performance of continuous monitoring TRO sen...
This document provides a method to ensure the performance of continuous monitoring TRO sensors, which can be installed in a BWMS or elsewhere in a ship, taking into consideration environmental factors associated with shipboard conditions, such as high salinity, vibration, variation in humidity and temperature, and predictable sea conditions. This document is intended for use by BWMS manufacturers…
1 Scope
This document specifies requirements for the information to be provided by the medical device manufacturer for the processing of critical or semi-critical medical devices (i.e. a medical device that enters normally sterile parts of the human body or a medical device that comes into contact with mucous membranes or non-intact skin) or medical devices that are intended to be sterilized.…
Processing of health care products — Information to be provided by the medical device manufacturer f...
1 Scope
This document specifies requirements for the information to be provided by the medical device manufacturer for the processing of non-critical medical devices not intended to be sterilized (i.e. a medical device that is intended to come into contact with intact skin only or a medical device not intended for direct patient contact).
This includes information for processing prior to use or…