Table of Contents

FOREWORD
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 of 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
202 Electromagnetic compatibility - Requirements and tests
208 General requirements, tests and guidance for alarm
    systems in medical electrical equipment and medical
    electrical systems
Annexes
Annex AA (informative) - Particular guidance and rationale
Annex BB (informative) - Alarm diagrams 208/IEC 60601-1-8:2006
Bibliography
Index of defined terms used in this particular standard

Abstract

Pertains to BASIC SAFETY and ESSENTIAL PERFORMANCE of INVASIVE BLOOD PRESSURE MONITORING EQUIPMENT, hereinafter referred to as ME EQUIPMENT.

General Product Information

Published
Document Type	Standard
Status	Current
Publisher	Canadian Standards Association
Pages
ISBN