CSA C22.2 No. 601.2.23 : 1998

FOREWORD
INTRODUCTION
SECTION ONE: GENERAL
1 Scope
2 Terminology and definitions
3 General requirements
4 General requirements for tests
5 Classification
6 Identification, marking and documents
SECTION TWO: ENVIRONMENTAL CONDITIONS
SECTION THREE: PROTECTION AGAINST ELECTRIC SHOCK HAZARDS
14 Requirements related to classification
17 Separation
19 Continuous leakage currents and patient auxiliary
    currents
20 Dielectric strength
SECTION FOUR: PROTECTION AGAINST MECHANICAL HAZARDS
21 Mechanical strength
SECTION FIVE: PROTECTION AGAINST HAZARDS FROM UNWANTED OR
EXCESSIVE RADIATION
SECTION SIX: PROTECTION AGAINST EXCESSIVE TEMPERATURES
AND OTHER SAFETY HAZARDS
42 Excessive temperatures
44 Overflow, spillage, leakage, humidity, ingress of liquids,
    cleaning, sterilization and disinfection
SECTION EIGHT: ACCURACY OF OPERATING DATA AND PROTECTION
AGAINST HAZARDOUS OUTPUT
SECTION NINE: ABNORMAL OPERATION AND FAULT CONDITIONS,
ENVIRONMENTAL TESTS
SECTION TEN: CONSTRUCTIONAL REQUIREMENTS
56 Components and general assembly
57 Mains part, components and layout
Figures
101 Test for protection against defibrillator discharge
102 Measuring circuit for the patient leakage current from
    the applied part to earth of class 1 equipment, caused
    by an external voltage on a functional earth terminal
104 Foam block test
Appendix D Symbols on marking
Annex AA General guidance and rationale

Gives requirements for the safety of transcutaneous partial pressure monitoring equipment used with children, adults and neonates. It also covers fetal monitoring during birth using these devices.