Table of Contents
                            
                            
                            
                        
                    
                    
                        
                            
                            
                                
                                
                                    
		
		1 - 
		AS/NZS 3200.2.36:1998 APPROVAL AND TEST SPECIFICATION - MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR ....
		
		4 - 
		PREFACE
		
		
		6 - 
		CONTENTS
		
		
		7 - 
		INTRODUCTION
		
		
		9 - 
		1 Scope and object
		
		9 - 
		1.1 Scope
		
		
		9 - 
		1.2 Object
		
		
		9 - 
		1.3 Particular Standards
		
		
		
		10 - 
		2 Terminology and definitions
		
		10 - 
		2.1 EQUIPMENT parts, auxiliaries and ACCESSORIES
		
		10 - 
		2.1.101 EQUIPMENT FOR EXTRACORPOREALLY INDUCED LITHOTRIPSY
		
		
		
		10 - 
		2.12 Miscellaneous
		
		10 - 
		2.12.101 LITHOTRIPSY
		
		
		10 - 
		2.12.102 EXTRACORPOREALLY INDUCED LITHOTRIPSY
		
		
		11 - 
		2.12.103 PRESSURE PULSE
		
		
		11 - 
		2.12.104 PRESSURE PULSE COUPLING
		
		
		11 - 
		2.12.105 FOCAL VOLUME
		
		
		11 - 
		*2.12.106 LOCALIZATION DEVICE
		
		
		11 - 
		2.12.107 TARGET LOCATION
		
		
		11 - 
		2.12.108 POSITIONING DEVICE
		
		
		11 - 
		2.12.109 TARGET MARKER
		
		
		
		
		11 - 
		6 Identification, marking and documents
		
		11 - 
		6.3 Marking of controls and instruments
		
		11 - 
		6.3.101 Wireless remote control
		
		
		
		11 - 
		6.8 ACCOMPANYING DOCUMENTS
		
		11 - 
		6.8.2 Instructions for use
		
		
		12 - 
		*6.8.3 Technical description
		
		
		
		
		12 - 
		10 Environmental conditions
		
		12 - 
		10.2.1 Environment
		
		
		
		13 - 
		19 Continuous leakage currents and patient auxiliary currents
		
		13 - 
		19.1 General requirements
		
		
		13 - 
		19.3 Allowable values
		
		
		
		13 - 
		20 Dielectric strength
		
		13 - 
		20.3 Values of test voltages
		
		
		
		13 - 
		21 Mechanical strength
		
		13 - 
		21.3 Addition:
		
		14 - 
		*21.3.101 Safety factor
		
		
		
		15 - 
		21.6 PORTABLE and MOBILE EQUIPMENT shall withstand the stress caused by rough handling.
		
		
		
		15 - 
		22 Moving parts
		
		15 - 
		22.3 Addition:
		
		
		16 - 
		22.4 Addition:
		
		
		16 - 
		22.7 Addition after the fifth dash:
		
		
		
		16 - 
		24 Stability in normal use
		
		
		16 - 
		*26 Vibration and noise
		
		
		17 - 
		28 Suspended masses
		
		17 - 
		28.1 General
		
		
		17 - 
		28.3 Addition after the second dash
		
		
		
		17 - 
		*35 Acoustical energy (including ultrasonics)
		
		
		17 - 
		*36 Electromagnetic compatibility
		
		
		18 - 
		42 Excessive temperatures
		
		
		18 - 
		49 Interruption of the power supply
		
		18 - 
		49.2 Restoration of power supply
		
		
		
		18 - 
		50 Accuracy of operating data
		
		
		19 - 
		51 Protection against hazardous output
		
		
		19 - 
		54 General
		
		19 - 
		54.3 Inadvertent changing of settings
		
		
		
		20 - 
		56 Components and general assembly
		
		20 - 
		56.11 Cord-connected hand-held and foot-operated control devices
		
		
		
		20 - 
		57 Main parts, components and layout
		
		20 - 
		*57.10 CREEPAGE DISTANCES and AIR CLEARANCES
		
		
		
		21 - 
		Annexes
		
		
		21 - 
		Appendix L - References - Publications mentioned in this Standard
		
		
		22 - 
		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
                                     | 
                                     | 
                                
                                
			| 
                                        Document Type
                                     | 
			Standard | 
		
		
                                
			| 
                                        Status
                                     | 
			Current | 
		
		
                                
			| 
                                        Publisher
                                     | 
			
                                        
                                        Standards Australia 
                                     | 
		
		
                                
			| 
                                        ProductNote
                                     | 
			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
                                     | 
                                     | 
                                
                                
                                    | 
                                        ISBN
                                     | 
                                     | 
                                
                                
			| 
                                        Committee
                                     | 
			HE-003 | 
		
		
                                
                                
			| 
                                        Supersedes
                                     | 
			
                                        
                                     |