CSA C22.2 No. 601.2.19 : 1992
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR THE SAFETY OF BABY INCUBATORS
Hardcopy , PDF
01-11-2009
French
01-01-2001
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CSA Preface
CSA Foreword
Glossary of Equivalent Terms
Reference Publications
Canadian Deviations and Editorial Changes
IEC Standard 601.2.19 (1990)
Foreword
Preface
Introduction
Section One - General
1 Scope and Object
2 Terminology and Definitions
3 General Requirements
4 General Requirements for Tests
5 Classification
6 Identification, Marking and Documents
7 Power Input
Section Two - Safety Requirements
10 Special Environmental Conditions
11 Special Measures with Respect to Safety
Section Three - Protection Against Electric Shock
Hazards
20 Dielectrical Strength
Section Four - Protection Against Mechanical Hazards
21 Mechanical Strength
22 Moving Parts
23 Surfaces, Corners and Edges
24 Stability in NORMAL USE
Section Five - Protection Against Hazards From Unwanted
or Excessive Radiation
36 ELECTROMAGNETIC COMPATIBILITY
Section Six - Protection Against Hazards of Explosions
in Medically Used Rooms
Section Seven - Protection Against Excessive Temperatures,
Fire and other Hazards, such as Human
Errors
42 Excessive Temperatures
43 Fire Prevention
44 Overflow, Spillage, Leakage, Humidity, Ingress of
Liquids, Cleaning, Sterilization and Disinfection
45 Pressure Vessels and Parts Subject to Pressure
46 Human Errors
49 Interruption of the Power Supply
Section Eight - Accuracy of Operating Data and Protection
Against Incorrect Output
50 Accuracy of Operating Data
Section Ten - Constructional Requirements
54 General
55 Enclosures and Covers
56 Components and General Assembly
Section Eleven - Additional Requirements
101 Alarms
102 Sound Pressure Level
103 Humidifying unit
104 Maximum Air Velocity in the Enclosure
105 Concentration of Carbon Dioxide (CO[2])
Annexes
Appendix L - References - Publications mentioned in
this standard
Annex AA (informative) - General guidance and rationale
Specifies requirements for the safety of INCUBATORS as defined in Sub-clause 2.1.101, hereinafter referred to as EQUIPMENT and designed to be installed and used in accordance with the Rules of the Canadian Electrical Code, Part I.
| DevelopmentNote |
Amendment 1 is available separately, see CSA C22.2.601.2.19A. (05/2004)
|
| DocumentType |
Standard
|
| Pages |
46
|
| PublisherName |
Canadian Standards Association
|
| Status |
Superseded
|
| Supersedes |
| Standards | Relationship |
| IEC 60601-2-19:2009+AMD1:2016 CSV | Identical |
| IEC 60601-1:2005+AMD1:2012 CSV | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
| ISO 7767:1997 | Oxygen monitors for monitoring patient breathing mixtures — Safety requirements |
| IEC 60601-2-20:2009+AMD1:2016 CSV | Medical electrical equipment - Part 2-20: Particular requirements for the basic safety and essential performance of infant transportincubators |
| IEC 60601-1-2:2014 | Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests |
| IEC 60601-1-3:2008+AMD1:2013 CSV | Medical electrical equipment - Part 1-3: General requirements forbasic safety and essential performance - Collateral Standard: Radiation protection in diagnostic X-ray equipment |
| IEC 60601-1-4:1996+AMD1:1999 CSV | Medical electrical equipment - Part 1-4: General requirements for safety - Collateral Standard: Programmable electrical medical systems |
| IEC 60651:1979+AMD1:1993+AMD2:2000 CSV | Sound level meters |
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