CSA ISO 11196 : 0

Section 1 General
1.1 Scope
1.2 Normative references
1.3 Definitions
1.4 General requirements and general requirements for
     tests
1.5 Classification
1.6 Identification, marking and documents
1.7 Power input
Section 2 Environmental conditions
2.1 Basic safety categories
2.2 Removable protective means
2.3 Environmental conditions
Section 3 Protection against electric shock hazards
3.1 General
3.2 Requirements related to classification
3.3 Limitation of voltage and/or energy
3.4 Enclosures and protective covers
3.5 Separation
3.6 Protective earthing, functional earthing and
     potential equalization
3.7 Continuous leakage current and patient auxiliary
     currents
3.8 Dielectric strength
Section 4 Protection against mechanical hazards
4.1 Mechanical strength
4.2 Moving parts
4.3 Surface, corners and edges
4.4 Stability in normal use
4.5 Expelled parts
4.6 Vibration and noise
4.7 Pneumatic and hydraulic power
4.8 Suspended masses
Section 5 Protection against hazards from unwanted or
          excessive radiation
5.1 X-radiation
5.2 Alpha, beta, gamma, neutron radiation and other
     particle radiation
5.3 Microwave radiation
5.4 Light radiation (including lasers)
5.5 Infrared radiation
5.6 Ultraviolet radiation
5.7 Acoustical energy (including ultrasonics)
5.8 Electromagnetic compatibility
Section 6 Protection against hazards of ignition of
          flammable anaesthetic mixtures
6.1 Locations and basic requirements
6.2 Marking, accompanying documents
6.3 Common requirements for categories AP and APG
     equipment
6.4 Requirements and tests for category AP equipment,
     parts and components
6.5 Requirements and tests for category APG equipment,
     parts and components
Section 7 Protection against excessive temperatures
          and other safety hazards
7.1 Excessive temperatures
7.2 Fire prevention
7.3 Overflow, spillage, leakage, humidity, ingress of
     liquids, cleaning, sterilization and disinfection
7.4 Pressure vessels and parts subject to pressure
7.5 Human errors
7.6 Electrostatic charges
7.7 Materials in applied parts in contact with body of
     patient
7.8 Interruption of power supply
Section 8 Accuracy of operating data and protection
          against hazardous output
8.1 Accuracy of operating data
8.2 Protection against hazardous output
Section 9 Abnormal operation and fault conditions,
          environment tests
9.1 Abnormal operation and fault conditions
9.2 Environmental tests
Section 10 Constructional requirements
10.1 General
10.2 Enclosures and covers
10.3 Components and general assembly
10.4 Main parts, components and layout
10.5 Protective earthing - Terminals and connections
10.6 Construction and layout
Section 11 Additional requirements specific to
           anaesthetic gas monitors
11.1 Interfering gas and vapour effects (other than
     water vapour)
11.2 Obstruction of sampling tube
11.3 Breathing system connections
11.4 Contamination of breathing systems
Annexes
A to L
M Test of anaesthetic agents for non-flammability
N Rationale
P Bibliography

Defines requirements for anaesthetic gas monitors intended for use in determining the anaesthetic vapour and/or gas level(s) in breathing gas mixtures and/or fresh gas mixtures. Both diverting and non-diverting anaesthetic gas monitors are covered, irrespective of the measuring technology used.