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IEC 80001-1:2010 ED1

Application of risk management for IT-networks incorporating medical devices - Part 1: Roles, responsibilities and activities
27 tet 2010

General information

99.60     21 sht 2021

IEC

TC 62/SC 62A

International Standard

11.040.01     35.240.80  

anglisht   frëngjisht   spanjisht  

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Scope

IEC 80001-1:2010 Recognizing that medical devices are incorporated into IT-networks to achieve desirable benefits (for example, interoperability), defines the roles, responsibilities and activities that are necessary for risk management of IT-networks incorporating medical devices to address safety, effectiveness and data and system security (the key properties). IEC 80001-1:2010 does not specify acceptable risk levels. IEC 80001-1:2010 applies after a medical device has been acquired by a responsible organization and is a candidate for incorporation into an IT-network. It applies throughout the life cycle of IT-networks incorporating medical devices. IEC 80001-1:2010 applies where there is no single medical device manufacturer assuming responsibility for addressing the key properties of the IT-network incorporating a medical device. IEC 80001-1:2010 applies to responsible organizations, medical device manufacturers and providers of other information technology for the purpose of risk management of an IT-network incorporating medical devices as specified by the responsible organization. It does not apply to personal use applications where the patient, operator and responsible organization are one and the same person.

Life cycle

NOW

WITHDRAWN
IEC 80001-1:2010 ED1
99.60 Withdrawal effective
21 sht 2021

REVISED BY

PUBLISHED
IEC 80001-1:2021 ED2