torna su
close Close

CEI membership discount

Dear customer,
our systems show that your name is connected to a company associated with CEI: you would therefore be entitled to thediscount reserved for our members for CEI products and services. To check the validity of the association and benefit from the discounts, it is necessary to enter the register number assigned to your company in the box below.

You can continue shopping even without entering the membership register number, but you will not have access to dedicated discounts.

CONTINUE WITHOUT DISCOUNTS

The membership register number has been correctly entered.
From now on, after logging into your MyNorma account, you can purchase our products at the price reserved for our members.

doneCONTINUE PURCHASING
Current help_outline

IEC 62366-1:2015

Medical devices – Part 1: Application of usability engineering to medical devices
standard
ISO
ISO
Standard help_outline
Publication Date:  2015
Commitee:  ISO-TC210
Language:  EN
IEC 62366-1:2015 specifies a PROCESS for a MANUFACTURER to analyse, specify, develop and evaluate the USABILITY of a MEDICAL DEVICE as it relates to SAFETY. This USABILITY ENGINEERING (HUMAN FACTORS ENGINEERING) PROCESS permits the MANUFACTURER to assess and mitigate RISKS associated with CORRECT USE and USE ERRORS, i.e., NORMAL USE. It can be used to identify but does not assess or mitigate RISKS associated with ABNORMAL USE. This first edition of IEC 62366-1, together with the first edition of IEC 62366-2, cancels and replaces the first edition of IEC 62366 published in 2007 and its Amendment 1 (2014). Part 1 has been updated to include contemporary concepts of usability engineering, while also streamlining the process. It strengthens links to ISO 14971:2007 and the related methods of risk management as applied to safety related aspects of medical device user interfaces. Part 2 contains tutorial information to assist manufactures in complying with Part 1, as well as offering more detailed descriptions of usability engineering methods that can be applied more generally to medical devices that go beyond safety-related aspects of medical device user interfaces.

International Coding Standard (ICS)

11.040.01
Medical equipment in general

Annotation

PLEASE NOTE: links will be automatically recognized and made clickable when the annotation will be published

Standard Evolution

close

ICS

International Classification for Standards (ICS) is an international classification system for technical standards.

The ICS is a hierarchical classification organized on three levels.

Level 1 covers the main fields of activity in standardization, e.g. road vehicle engineering, agriculture, metallurgy.

Each field has a two-digit notation, e.g.

  43    Road Vehicle Engineering

The main fields are subdivided into groups (level 2). The notation of a group consists of the field notation and a three-digit group number, separated by a point, e.g.

  43.040    Road vehicle systems

Some groups are further divided into sub-groups (level 3). The notation of a sub-group consists of the group notation and a two-digit number, separated by a point, e.g.

  43.040.20 Lighting, signaling and warning devices

You can identify the ICS code of your interest by typing the code or a keywordword in the dropdown ICS field, and by selecting one of the filtered results.

Search also in the summary/description of the standard

By flagging this control, the search for keywords will not be limited to the Standard Number and Title fields, but will also be performed in the Abstract of the standard.

This way, you will get more results.

You should use this option when you can not find the desired result with the standard approach and it is necessary to extend the scope of the search: by increasing the number of results, you will increase the number of non-relevant elements, as well.