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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…

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 Domaine d’application Le présent document spécifie les exigences relatives aux informations à fournir par le fabricant du dispositif médical pour le traitement des dispositifs médicaux critiques ou semi-critiques (c’est-à-dire un dispositif médical qui pénètre dans des sites normalement stériles du corps humain ou un dispositif médical qui entre en contact avec des muqueuses ou une peau lésée…

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 Domaine d’application Le présent document spécifie les exigences applicables aux informations relatives au traitement des dispositifs médicaux non critiques et non destinés à être stérilisés, à fournir par le fabricant du dispositif (c’est-à-dire un dispositif médical destiné à entrer en contact avec la peau intacte uniquement ou un dispositif médical qui n’est pas destiné à un contact direct…

1 Scope This document provides guidance for the application of the requirements contained in ISO 11607-1 and ISO 11607-2. It does not add to, or otherwise change, the requirements of ISO 11607-1 and ISO 11607-2. This is an informative document, not normative. It does not include requirements to be used as basis of regulatory inspection or certification assessment activities. The guidance can be…

1 Domaine d’application Le présent document fournit des recommandations pour l’application des exigences énoncées dans l’ISO 11607-1 et dans l’ISO 11607-2. Il ne complète ni ne modifie en aucune manière les exigences de l’ISO 11607-1 et de l’ISO 11607-2. Le présent document est informatif, et non normatif. Il n’inclut pas d’exigence à utiliser comme base pour les activités d’inspection…

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…