03/318598 DC : DRAFT NOV 2003

Foreword
Introduction
1 Scope
2 Normative references
3 Definitions
  3.1 Adverse event
  3.2 Adverse event cause
  3.3 Adverse event type
  3.4 Device nomenclature code
  3.5 Device type
  3.6 Patient/user outcome code
4 Coding system structure
5 Coding system requirements
  5.1 Device nomenclature code
  5.2 Device type
  5.3 Adverse event type code
  5.4 Adverse event cause code
  5.5 Patient/user outcome code
6 Coding system for adverse event reporting
Tables
Annex A (informative) Bibliography

ISO TS 19218