Table of Contents
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AS/NZS 3200.2.36:1998 APPROVAL AND TEST SPECIFICATION - MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR ....
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PREFACE
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CONTENTS
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INTRODUCTION
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1 Scope and object
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1.1 Scope
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1.2 Object
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1.3 Particular Standards
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2 Terminology and definitions
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2.1 EQUIPMENT parts, auxiliaries and ACCESSORIES
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2.1.101 EQUIPMENT FOR EXTRACORPOREALLY INDUCED LITHOTRIPSY
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2.12 Miscellaneous
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2.12.101 LITHOTRIPSY
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2.12.102 EXTRACORPOREALLY INDUCED LITHOTRIPSY
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2.12.103 PRESSURE PULSE
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2.12.104 PRESSURE PULSE COUPLING
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2.12.105 FOCAL VOLUME
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*2.12.106 LOCALIZATION DEVICE
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2.12.107 TARGET LOCATION
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2.12.108 POSITIONING DEVICE
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2.12.109 TARGET MARKER
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6 Identification, marking and documents
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6.3 Marking of controls and instruments
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6.3.101 Wireless remote control
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6.8 ACCOMPANYING DOCUMENTS
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6.8.2 Instructions for use
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*6.8.3 Technical description
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10 Environmental conditions
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10.2.1 Environment
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19 Continuous leakage currents and patient auxiliary currents
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19.1 General requirements
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19.3 Allowable values
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20 Dielectric strength
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20.3 Values of test voltages
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21 Mechanical strength
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21.3 Addition:
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*21.3.101 Safety factor
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21.6 PORTABLE and MOBILE EQUIPMENT shall withstand the stress caused by rough handling.
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22 Moving parts
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22.3 Addition:
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22.4 Addition:
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22.7 Addition after the fifth dash:
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24 Stability in normal use
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*26 Vibration and noise
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28 Suspended masses
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28.1 General
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28.3 Addition after the second dash
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*35 Acoustical energy (including ultrasonics)
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*36 Electromagnetic compatibility
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42 Excessive temperatures
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49 Interruption of the power supply
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49.2 Restoration of power supply
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50 Accuracy of operating data
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51 Protection against hazardous output
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54 General
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54.3 Inadvertent changing of settings
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56 Components and general assembly
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56.11 Cord-connected hand-held and foot-operated control devices
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57 Main parts, components and layout
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*57.10 CREEPAGE DISTANCES and AIR CLEARANCES
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Annexes
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Appendix L - References - Publications mentioned in this Standard
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Annex AA - General guidance and rationale
Abstract
Specifies safety requirements for the design and manufacture of devices (lithotripters) intended to generate acoustic pulses from outside the human body for the purpose of fragmenting calculi ('stones') within the body. This Standard is to be read in conjunction with AS 3200.1.0-1990. It is identical with and reproduced from IEC 60601-2-36:1997.
Scope
This clause of the General Standard applies except as follows: 1.1 Scope Addition:
This Particular Standard applies to the safety of EQUIPMENT FOR EXTRACORPOREALLY INDUCED LITHOTRIPSY as defined in 2.1.101. The applicability of this Particular Standard is limited to components directly involved in the LITHOTRIPSY treatment, such as, but not limited to, the generator of the PRESSURE PULSE, PATIENT support device, and their interactions with imaging and monitoring devices. Other devices, such as PATIENT treatment planning computers, X-ray and ultrasonic devices, are excluded from this Standard, because they are treated in other applicable IEC standards. While this Particular Standard has been developed for EQUIPMENT intended for use in LITHOTRIPSY, it has been developed such that, as long as no other specific standards are available to be used for other medical applications of therapeutic extracorporeal PRESSURE PULSE equipment, this Standard may be used as a guideline.
General Product Information
Published
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Document Type
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Standard |
Status
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Current |
Publisher
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Standards Australia
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ProductNote
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Pending Revision indicates that as a result of the Aged Standards review process, the document needs updating. If no project proposal, meeting the quality criteria, is received within the 12 month timeframe, the document shall be withdrawn. |
Pages
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ISBN
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Committee
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HE-003 |
Supersedes
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