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CSA C22.2 No. 60601.2.30 : 2002

Withdrawn

Withdrawn

A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.

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MEDICAL ELECTRICAL EQUIPMENT - PART 2: PARTICULAR REQUIREMENTS FOR THE SAFETY OF AUTOMATIC CYCLING INDIRECT BLOOD PRESSURE MONITORING EQUIPMENT

Available format(s)

Hardcopy , PDF

Withdrawn date

24-08-2016

Language(s)

English

Published date

01-01-2011

€207.28
Excluding VAT

FOREWORD
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
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
 22 Moving parts
SECTION FIVE - PROTECTION AGAINST HAZARDS FROM UNWANTED
                OR EXCESSIVE RADIATION
 36 ELECTROMAGNETIC COMPATIBILITY
SECTION SIX - PROTECTION AGAINST HAZARDS OF IGNITION OF
                FLAMMABLE ANAESTHETIC MIXTURES
SECTION SEVEN - PROTECTION AGAINST EXCESSIVE TEMPERATURES
                AND OTHER SAFETY HAZARDS
 42 Excessive temperatures
 44 Overflow, spillage, leakage, humidity, ingress of
    liquids, cleaning, sterilization and disinfection
 45 Pressure vessels and parts subject to PRESSURE
 49 Interruption of the power supply
SECTION EIGHT - ACCURACY OF OPERATING DATA AND
                PROTECTION AGAINST HAZARDOUS OUTPUT
 50 Accuracy of operating data
 51 Protection against hazardous output
SECTION NINE - ABNORMAL OPERATION AND FAULT CONDITIONS,
                ENVIRONMENTAL TESTS
SECTION TEN - CONSTRUCTIONAL REQUIREMENTS
 56 Components and general assembly
 57 MAINS PARTS, components and layout
Figures
APPENDIX D - Symbols on marking
Annexes
AA (informative) - General guidance and rationale
BB (informative) - Graphical representation of the
                   permissible operating areas of
                   the EQUIPMENT in NORMAL and SINGLE
                   FAULT CONDITIONS

Covers important safety requirements for blood pressure monitoring equipment. Does not apply to blood pressure equipment which uses finger transducers or semi-automatic blood pressure measuring equipment, typically in which each determination needs to be initiated manually.

DocumentType
Standard
Pages
56
PublisherName
Canadian Standards Association
Status
Withdrawn
SupersededBy
Supersedes

Standards Relationship
IEC 60601-2-30:1999 Identical

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