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This document specifies the form and meaning of programs written in Ada. Its purpose is to promote the portability of Ada programs to a variety of computing systems. This document specifies: —   The form of a program written in Ada; —   The effect of translating and executing such a program; —   The manner in which program units can be combined to form Ada programs; —   The language-defined…

IEC 62899-202:2023 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy way to compare all the changes between the official IEC Standard and its previous edition. IEC 62899-202:2023 defines the terms and specifies the standard test methods for characterization and evaluation of…

This document specifies the form and meaning of programs written in Ada. Its purpose is to promote the portability of Ada programs to a variety of computing systems. This document specifies: — The form of a program written in Ada; — The effect of translating and executing such a program; — The manner in which program units can be combined to form Ada programs; — The language-defined…

IEC 62899-202:2023 defines the terms and specifies the standard test methods for characterization and evaluation of conductive inks. This document also provides measurement methods for evaluating the properties of conductive layers made both from an additive process using conductive inks and from a subtractive process used in printed electronics. This edition includes the following significant…

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.…

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…

1 Scope 1.1 Introduction This Standard describes the test procedures, test set-ups, and calculations required to determine the performance, capacities, energy consumption, and overall efficiency of gas-fired and oil-fired combined radiant space and water heating systems (combos) with hydronic heat distribution. 1.2 Type of standard This Standard establishes laboratory methods for testing and…

1 Scope 1.1 General This Standard applies to free-standing, selective-type storage racks where the principal structural components are upright frames and load support beams. These storage racks include selective racks, double-deep racks, very narrow aisle (VNA) racks, push-back racks, pallet-flow racks, pallet shuttle racks, and automated storage and retrieval system (AS/RS) racks. Note:…

1 Scope 1.1 General 1.1.1 Application This Standard applies to hyperbaric chambers that have as their primary function the subjection of humans to pressure environments exceeding 1 atmosphere absolute, such as those required in a) diving operations; b) work under compressed-air conditions; c) medical treatment; d) training; and e) research. 1.1.2 Minimum requirements This Standard…

1 Scope 1.1 General This Standard assesses the performance of package wastewater treatment plants that are intended to treat either mixed-wastewater or greywater drainage and produce a treated effluent water quality suitable for non-potable water reuse applications with a treatment capacity of up to 10 000 L/d (2650 gal/d) or less. This Standard also covers site-assembled components included…