Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 General requirements
4.1 Proposal of symbols for adoption
4.2 Requirements for usage
5 Symbols
5.1 Manufacture
5.2 Sterility
5.3 Storage
5.4 Safe Use
5.5 IVD-specific
5.6 Transfusion/infusion
5.7 Other
Annex A (informative) - Examples
Annex B (informative) - Use of general prohibition symbol
and negation symbol
Annex ZA (informative) - Clauses of this European Standard
addressing essential requirements or other
provisions of the Council Directive 93/42/EEC
concerning medical devices
Annex ZB (informative) - Relationship between this European
Standard and the Essential Requirements of EU
Directive 90/385/EEC on Active Implantable Medical
Devices
Annex ZC (informative) - Relationship between this European
Standard and the Essential Requirements of EU
Directive 98/79/EC on In vitro Diagnostic Medical
Devices
Bibliography