By Kenneth G.Munson
;Caravelle three & 6 [Aircraft Profile a hundred and eighty] КНИГИ ;ТЕХНИКА Название: Caravelle three & 6Автор:Kenneth G.Munson Серия: airplane Profile a hundred and eighty Издательство: Profile courses Ltd Год издания: 1967 Страниц:16 Формат: PDF в rarЯзык: английский Размер: 10.90 Мб Для сайта: Мир книгФранцузские пассажирские турбореактивные самолеты Caravelle производились с 1955 года и все еще встречались на пассажирских маршрутах в конце 90-х. Особенностью самолета было размещение двигателей в хвосте самолетаifolder.ru.com zero
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It is also, for the time being, and for several reasons, impossible to provide standards, even urgently needed, for a number of kinds of MEDICAL ELECTRICAL EQUIPMENT. Standardization bodies, including those outside IEC, have taken over the system of this IEC Publication in order to have an unique system of standards. In such cases it is most important to give a guideline in this section as a help towards ″functional″ PATIENT safety. 9 Abnormal operation and fault conditions; environmental tests EQUIPMENT or parts of EQUIPMENT may cause, due to abnormal operation, excessive temperatures or other Therefore these abnormal operations or fault conditions must be investigated.
In this hypothetical case the PATIENT is supposed not to be connected to the APPLIED PART. Clause 4 In EQUIPMENT there may be many pieces of insulation, components (electrical and mechanical) and constructional features in which a failure would not produce a SAFETY HAZARD to PATIENT, OPERATOR or surroundings, even though causing a deterioration in or a failure of performance of EQUIPMENT. 1 In order to ensure that every individually produced item of EQUIPMENT conforms to this Standard, the manufacturer and/or installer should carry out such measures during manufacture and/or installation assembly as to ensure that each item satisfies all requirements even if it is not completely tested individually during manufacture or installation.
Firstly, if contact is essential for the NORMAL USE of the EQUIPMENT, the part is subject to the requirements for APPLIED PARTS. If contact is incidental to the functioning of the EQUIPMENT, the part is categorized according to whether contact results from deliberate action by the PATIENT or by the OPERATOR. Where contact is incidental and results from action by the PATIENT, the PATIENT is in most respects no more at risk than any other person, so the requirements for ENCLOSURES are sufficient.