CEI EN 80601-2-30/A1 Medical electrical equipment Part 2: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers
Данный раздел/документ содержится в продуктах:
- Техэксперт: Машиностроительный комплекс
- Картотека зарубежных и международных стандартов
- CEI EN 60601-1-10/A1 Medical electrical equipment Part 1: General requirements for basic safety and essential performance - Collateral Standard: Requirements for the development of physiologic closed-loop controllers
- 11
- CEI EN 60601-1-10/A1 Medical electrical equipment Part 1: General requirements for basic safety and essential performance - Collateral Standard: Requirements for the development of physiologic closed-loop controllers
- 11.040
- CEI EN 60601-1-10/A1 Medical electrical equipment Part 1: General requirements for basic safety and essential performance - Collateral Standard: Requirements for the development of physiologic closed-loop controllers
- CEI EN 60601-2-33/A1/A2 Medical electrical equipment Part 2: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis
- 11.040.55
- CEI EN 60601-2-33/A1/A2 Medical electrical equipment Part 2: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis
- CEI EN 60601-2-33/A1/A2 Medical electrical equipment Part 2: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis
- CEI EN 60601-1-6/A1 Medical electrical equipment Part 1: General requirements for basic safety and essential performance - Collateral standard: Usability
- Картотека зарубежных и международных стандартов
Comitato Elettrotecnico Italiano
Medical electrical equipment Part 2: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers
N EN 80601-2-30/A1
Annotation
INTRODUCTION TO THE AMENDMENT
This amendment deals primarily with editorial corrections and clarifications, clarifies requirements for operation in the loss of SUPPLY MAINS and references new and updated collateral standards.
To meet needs for change which were identified by users of this particular standard, it was necessary to amend the standard before the previously approved maintenance cycle date.
Автоматический перевод:
Медицинская Часть 2 электрооборудования: Конкретные требования для основной безопасности и существенной производительности автоматизированных атравматичных сфигмоманометров
ВВЕДЕНИЕ В ПОПРАВКУ
Эта поправка соглашения, прежде всего, с редакционными исправлениями и разъяснениями, разъясняет требования для эксплуатации в потере SUPPLY MAINS и новых ссылок и обновила сопутствующие стандарты.
Для удовлетворения потребностей для изменения, которые были идентифицированы пользователями этого конкретного стандарта было необходимо исправить стандарт перед ранее утвержденной датой цикла техобслуживания.
