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Homepage>BS Standards>11 HEALTH CARE TECHNOLOGY>11.040 Medical equipment>11.040.01 Medical equipment in general>BS ISO 16142-2:2017 Medical devices. Recognized essential principles of safety and performance of medical devices General essential principles and additional specific essential principles for all IVD medical devices and guidance on the selection of standards
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immediate downloadReleased: 2017-09-20
BS ISO 16142-2:2017 Medical devices. Recognized essential principles of safety and performance of medical devices General essential principles and additional specific essential principles for all IVD medical devices and guidance on the selection of standards

BS ISO 16142-2:2017

Medical devices. Recognized essential principles of safety and performance of medical devices General essential principles and additional specific essential principles for all IVD medical devices and guidance on the selection of standards

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Standard number:BS ISO 16142-2:2017
Pages:52
Released:2017-09-20
ISBN:978 0 580 91385 3
Status:Standard
DESCRIPTION

BS ISO 16142-2:2017


This standard BS ISO 16142-2:2017 Medical devices. Recognized essential principles of safety and performance of medical devices is classified in these ICS categories:
  • 11.040.01 Medical equipment in general

This document, which includes the essential principles of safety and performance, identifies significant standards and guides that can be used in the assessment of conformity of a medical device to the recognized essential principles that when met, indicate a medical device is safe and performs as intended. This document identifies and describes the six general essential principles of safety and performance (see Table B.1) that apply to all medical devices, including IVD medical devices (in vitro diagnostic).

This document also identifies and describes the additional essential principles of safety and performance which need to be considered during the design and manufacturing process, which are relevant to IVD medical devices.

NOTE During the design process, the manufacturer selects which of the listed design and manufacturing principles apply to the particular medical device and documents the reasons for excluding others.

This document is intended for use as guidance by medical devicemanufacturers, standards development organizations, authorities having jurisdiction, and conformity assessment bodies.


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