AS/NZS 3200.2.30:1996

1 - AS/NZS 3200.2.30:1996 APPROVAL AND TEST SPECIFICATION-MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR SAFETY-AUTOMATI
4 - PREFACE
5 - CONTENTS
7 - SECTION ONE - GENERAL
7 - 1 Scope and object
7 - 1.1 Scope
7 - 1.2 Object
7 - 1.3 Particular Standards
8 - 2 Terminology and definitions
9 - 3 General requirements
9 - 4 General requirements for tests
9 - 5 Classification
10 - 6 Identification, marking and documents
11 - SECTION THREE - PROTECTION AGAINST ELECTRIC SHOCK HAZARDS
11 - 14 Requirements related to classification
11 - 17 Separation
12 - 19 Continuous leakage currents and patient auxiliary currents
13 - 20 Dielectric strength
13 - SECTION FOUR - PROTECTION AGAINST MECHANICAL HAZARDS
13 - 21 Mechanical strength
13 - 22 Moving parts
15 - SECTION FIVE - PROTECTION AGAINST HAZARDS FROM UNWANTED OR EXCESSIVE RADIATION
15 - 34 Ultraviolet radiation
15 - SECTION SIX - PROTECTION AGAINST HAZARDS OF IGNITION OF FLAMMABLE ANAESTHETI C MIXTURES
15 - SECTION SEVEN - PROTECTION AGAINST EXCESSIVE TEMPERATURES AND OTHER SAFETY HAZARDS
15 - 42 Excessive temperatures
16 - 44 Overflow, spillage, leakage, humidity, ingress of liquids, cleaning, sterilizationand disinfection
16 - 45 Pressure vessels and parts subject to pressure
16 - 49 Interruption of the power supply
17 - SECTION EIGHT - ACCURACY OF OPERATING DATA AND PROTECTION AGAINST HAZARDOUS OUTPUT
17 - 51 Protection against hazardous output
18 - SECTION NINE - ABNORMAL OPERATION AND FAULT CONDITIONS, ENVIRONMENTAL TESTS
18 - SECTI ON TEN - CONSTRUCTIONAL REQUIREMENTS
18 - 56 Components and general assembly
18 - 57 Mains parts, components and layout
23 - APPENDIX D - Symbols on marking
24 - Annex AA - General guidance and rationale
24 - General
25 - Use with defibrillator
25 - Rationale for defibrillator test voltages
26 - Summary
26 - Specific requirement
27 - Guidance and rationale for particular subclauses
32 - Annex BB - Graphical representation of the permissible operating areas of the equipment in normal and single fault conditions

Specifies particular safety requirements for automatic cycling indirect blood pressure monitoring equipment, with special attention being paid to the avoidance of hazards which may occur during the inflation of the cuff. This Standard is to be read in conjunction with AS 3200.1.0-1990. It is identical with and reproduced from IEC 601-2-30:1995.

Addition:This Standard specifies the particular safety requirements for AUTOMATIC CYCLING INDIRECT BLOOD PRESSURE MONITORING EQUIPMENT as defined in 2.101 and hereinafter also referred to as EQUIPMENT.This Particular Standard does not apply to blood pressure measuring equipment which uses finger transducers or to semi-automatic bloodpressure measuring equipment(typically in which each determination needs to be initiated manually).

First published as AS/NZS 3200.2.30:1996.