CEI EN 60601-2-22 : 2014

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
ANNEX D (INFORMATIVE) - SYMBOLS ON MARKING
ANNEX AA (INFORMATIVE) - PARTICULAR GUIDANCE AND RATIONALE
BIBLIOGRAPHY
INDEX OF DEFINED TERMS USED IN THIS PARTICULAR STANDARD
ANNEX ZA (NORMATIVE) - NORMATIVE REFERENCES
                       TO INTERNATIONAL PUBLICATIONS
                       WITH THEIR CORRESPONDING
                       EUROPEAN PUBLICATIONS

This standard applies to the basic safety and performance of laser products for surgical, therapeutic, medical-diagnostic, cosmetic or veterinary applications intended for use on humans or animals classified as class 3B or 4 products and defined in EN/IEC 60825-1.