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SN EN 60601-2-36 : 1997

Withdrawn

Withdrawn

A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.

View Superseded by

MEDICAL ELECTRICAL EQUIPMENT - PART 2: PARTICULAR REQUIREMENTS FOR THE SAFETY OF EQUIPMENT FOR EXTRACORPOREALLY INDUCED LITHOTRIPSY

Withdrawn date

22-05-2018

Superseded by

SN EN 60601-2-36:2015

Published date

12-01-2013

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INTRODUCTION
SECTION ONE: GENERAL
1 Scope and object
2 Terminology and definitions
6 Identification, marking and documents
SECTION TWO: ENVIRONMENTAL CONDITIONS
10 Environmental conditions
SECTION THREE: PROTECTION AGAINST ELECTRIC SHOCK HAZARDS
19 Continuous Leakage Currents and patient auxiliary
    currents
SECTION FOUR: PROTECTION AGAINST MECHANICAL HAZARDS
21 Mechanical strength
22 Moving parts
24 Stability in normal use
26 Vibration and noise
28 Suspended masses
SECTION FIVE: PROTECTION AGAINST HAZARDS FROM UNWANTED
OR EXCESSIVE RADIATION
35 Acoustical energy (including ultrasonics)
36 Electromagnetic compatibility
SECTION 7: PROTECTION AGAINST EXCESSIVE TEMPERATURES AND
OTHER SAFETY HAZARDS
42 Excessive temperatures
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 TEN: CONSTRUCTIONAL REQUIREMENTS
54 General
56 Components and general assembly
57 Mains parts, components and layout
Annexes
L References - Publications mentioned in this Standard
AA General guidance and rationale
ZA (normative) Normative references to international
publications with their corresponding European publications
ZB (informative) Normative references to international
publications with their corresponding European publications

Applicable to the safety of equipment for extracorporeally induced lithotripsy. Limited to components directly involved in lithotripsy treatment, eg the generator of the pressure pulse, patient support device and interactions with imaging and monitoring devices.

DocumentType
Standard
PublisherName
Swiss Standards
Status
Withdrawn
SupersededBy

Standards Relationship
BS EN 60601-2-36:2015 Identical
I.S. EN 60601-2-36:2015 Identical
DIN EN 60601-2-36 : 2015 Identical
EN 60601-2-36:2015 Identical
IEC 60601-2-36:2014 Identical
UNE-EN 60601-2-36:1998 Identical

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