CSA C22.2 No. 80601-2-56 : 2012 : R2016
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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MEDICAL ELECTRICAL EQUIPMENT - PART 2-56: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF CLINICAL THERMOMETERS FOR BODY TEMPERATURE MEASUREMENT
Hardcopy , PDF
25-09-2021
English, French
01-01-2016
Foreword
Introduction
201.1 Scope, object and related standards
201.2 Normative references
201.3 Terminology and definitions
201.5 General requirements for testing of ME EQUIPMENT
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
201.101 Laboratory performance requirements
201.102 Clinical accuracy validation
201.103 Probes, probe cable extenders and probe covers
202 Medical electrical equipment - Part 1-2: General
requirements and essential performance - Collateral
standard: Electromagnetic compatibility - Requirements
and tests
Annexes
Annex C (informative) - Guide to marking and labelling
requirements for ME EQUIPMENT and ME SYSTEMS
Annex D (informative) - Symbols on Marking
Annex AA (informative) - Particular Guidance and rationaleale
Annex BB (informative) - REFERENCE TEMPERATURE SOURCE
Annex CC (informative) - Environmental aspects
Annex DD (informative) - Reference to the essential
principles of safety and medical devices in
accordance with ISO/TR 16142
Bibliography
Alphabetized index of defined terms used in this particular
standard
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