09/30175700 DC : 0

201.1 Scope, object and related standards
201.2 Normative references
201.3 Terms and definitions
201.4 General requirements
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
202 Medical electrical equipment - Part 1-2: General
    requirements for safety - Collateral standard:
    Electromagnetic compatibility - Requirements and
    tests
203 Medical electrical equipment - Part 1: General
    requirements for safety - 3. Collateral standard:
    General requirements for radiation protection in
    diagnostic X-ray equipment
206 Medical electrical equipment - Part 1-6: General
    requirements for safety - Collateral standard:
    Usability
208 Medical electrical equipment - Part 1-8: General
    requirements for safety - Collateral Standard:
    General requirements, tests and guidance for
    alarm systems in medical electrical equipment
    and medical electrical systems
209 Medical electrical equipment - Part 1-9: Medical
    electrical equipment - Part 1-9: General requirements
    for basic safety and essential performance - Collateral
    Standard: Requirements for the reduction of
    environmental impacts
210 Medical electrical equipment - Part 1-10: Medical
    electrical equipment - Part 1-10: General requirements
    for basic safety and essential performance - Collateral
    Standard: Process requirements for the development
    of therapeutic closed-loop controllers
Annex G (normative) - Protection against hazards of
                      ignition of flammable anaesthetic
                      mixtures
Annex AA (informative) - Particular guidance and rationale