Medical devices -- Risk management -- Part 1: Application of risk analysis

Available format(s)

Hardcopy , PDF

Language(s)

Japanese, English

Published date

28-02-2001

Publisher

Japanese Standards Association

1 -
2 -
3 -
4 -
5 -
6 -
7 -
8 -
9 -
10 -
11 -
12 -
13 -
14 -
15 -
16 -
17 -
18 -
19 -
20 -
21 -
22 -

This part of JIS Q 14971 specifies a procedure for investigating, using available information, the safety of a medical device, including in vitro diagnostic devices (IVD) or accessories, by identifying hazards and estimating the risks associated with the device.

DocumentType	Standard
Pages	0
PublisherName	Japanese Standards Association
Status	Current

Standards	Relationship
ISO 14971-1:1998	Identical

Reaffirmed 2015 2001(R2015) [26/10/2015]2001(R2009) [25/04/2009]2001 [25/02/2001]

View more information

$70.47

Including GST where applicable

Product format

I agree to the DRM document license rules apply against the PDF selection made.

Please confirm that you agree to the document license rules for this document.

I agree to the document license rules .

Please confirm that you agree to the document license rules for this document.

Access your standards online with a subscription

Features

Simple online access to standards, technical information and regulations.
Critical updates of standards and customisable alerts and notifications.
Multi-user online standards collection: secure, flexible and cost effective.

Learn more on subscription solutions

Get in touch with us

JIS Q 14971-1:2001

Medical devices -- Risk management -- Part 1: Application of risk analysis

Table of Contents

Abstract

General Product Information

International Equivalents

History

Category

Subcategory