2. Getting involved
3. Standards Committees
4. NAGESUTECH

DIN Standards Committee Health Technologies

Overview

This standard defines the life cycle requirements for medical device software. The set of processes, activities, and tasks described in this standard establishes a common framework for medical device software life cycle processes. This standard applies to the development and maintenance of medical device software when the software itself is a medical device or when the software is an embedded or integral part of the finished medical device. The responsible subcommittee is DKE/UK 811.3 "Sicherheit von medizinisch genutzten Geräten/Systemen/Einrichtungen in der vernetzten Anwendung" ("Safety of medical devices/systems/facilities for network applications") of the DKE (German Commission for Electrical, Electronic and Information Technologies) at DIN.

Document: references other documents

Document: referenced in other documents

Responsible national committee

DKE/UK 811.3 - Sicherheit von medizinisch genutzten Geräten/Systemen/Einrichtungen in der vernetzten Anwendung  

Responsible international committee

ISO/TC 210/JWG 2 - Joint ISO/TC 210-IEC/SC 62A WG : Medical device software