INTRODUCTION
201.1 SCOPE, OBJECT AND RELATED STANDARDS
201.2. NORMATIVE REFERENCES
201.3. TERMS AND DEFINITIONS
201.4. GENERAL REQUIREMENTS
201.5. GENERAL REQUIREMENTS FOR TESTING ME
EQUIPMENT
201.6. CLASSIFICATION OF ME EQUIPMENT AND ME
SYSTEMS
201.7. ME EQUIPMENT IDENTIFICATION, MARKING
AND DOCUMENTS
201.8. PROTECTION AGAINST ELECTRICAL HAZARDS
FROM ME EQUIPMENT
201.9. PROTECTION AGAINST MECHANICAL HAZARDS
OF ME EQUIPMENT AND ME SYSTEMS
201.10. PROTECTION AGAINST UNWANTED AND
EXCESSIVE RADIATION HAZARDS
201.11. PROTECTION AGAINST EXCESSIVE TEMPERATURES
AND OTHER HAZARDS
201.12. ACCURACY OF CONTROLS AND INSTRUMENTS AND
PROTECTION AGAINST HAZARDOUS OUTPUTS
201.13. HAZARDOUS SITUATIONS AND FAULT CONDITIONS
201.14. PROGRAMMABLE ELECTRICAL MEDICAL SYSTEMS (PEMS)
201.15. CONSTRUCTION OF ME EQUIPMENT
201.16. ME SYSTEMS
201.17. ELECTROMAGNETIC COMPATIBILITY OF ME EQUIPMENT
AND ME SYSTEMS
203. RADIATION PROTECTION IN DIAGNOSTIC X-RAY EQUIPMENT
ANNEX
ANNEX AA (INFORMATIVE) - TEST OF X-RAY TUBE ASSEMBLIES FOR
PRESSURE-RELATED RISKS
BIBLIOGRAPHY
INDEX OF DEFINED TERMS USED IN THIS PARTICULAR STANDARD
ANNEX ZA (NORMATIVE) - NORMATIVE REFERENCES
TO INTERNATIONAL PUBLICATIONS
WITH THEIR CORRESPONDING
EUROPEAN PUBLICATIONS