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09/30155521 DC : 0

Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View Superseded by
superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

BS EN 60601-1-11 ED.1 - MEDICAL ELECTRICAL EQUIPMENT - PART 1-11: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - COLLATERAL STANDARD: REQUIREMENTS FOR MEDICAL ELECTRICAL EQUIPMENT AND MEDICAL ELECTRICAL SYSTEMS USED IN THE HOME HEALTHCARE ENVIRONMENT

Available format(s)

Hardcopy , PDF

Superseded date

31-07-2010

Language(s)

English

FOREWORD
INTRODUCTION
1 Scope, object and related standards
   1.1 Scope
   1.2 Object
   1.3 Related standards
2 Normative references
3 Terms and definitions
4 General requirements
   4.1 Additional requirements for SUPPLY MAINS
       for ME EQUIPMENT and ME SYSTEMS
   4.2 Environmental conditions for ME EQUIPMENT
5 General requirements for testing ME EQUIPMENT
6 Classification of ME EQUIPMENT and ME SYSTEMS
7 ME EQUIPMENT identification, marking and documents
   7.1 USABILITY of the ACCOMPANYING DOCUMENTS
   7.2 Additional requirements for marking of IP
       classification
   7.3 ACCOMPANYING DOCUMENTS
   7.4 Instructions for use
   7.5 Technical description
8 Protection against excessive temperatures
   and other HAZARDS
   8.1 Additional requirements for cleaning, disinfection
       of ME EQUIPMENT and ME SYSTEMS
   8.2 Additional requirements for sterilization of ME
       EQUIPMENT and ME SYSTEMS
   8.3 Additional requirements for ingress of water or
       particulate matter into ME EQUIPMENT and ME SYSTEMS
   8.4 Additional requirements for interruption of the power
       supply/SUPPLY MAINS to ME EQUIPMENT
9 Accuracy of controls and instruments and protection against
   hazardous outputs
10 Construction of ME EQUIPMENT
   10.1 Additional requirements for mechanical strength
   10.2 Additional requirements for an INTERNAL ELECTRICAL
        POWER SOURCE
   10.3 Additional requirements for actuating parts of controls
        of ME EQUIPMENT
11 Protection against strangulation or asphyxiation
12 Additional requirements for electromagnetic compatibility
   of ME EQUIPMENT and ME SYSTEMS
   12.1 Additional technical description requirements
        applicable to ME EQUIPMENT and ME SYSTEMS
   12.2 Additional requirements applicable to ME EQUIPMENT
        and ME SYSTEMS specified for use only in a shielded
        location
  12.3 Additional requirements for ELECTROSTATIC DISCHARGE
       (ESD) tests
Annex A (informative) - General guidance and rationale
Annex B (informative) - Guide to marking and labelling
        requirements for ME EQUIPMENT and ME SYSTEMS
Bibliography
Index of defined terms used in this collateral standard

BS EN 60601-1-11 ED.1

Committee
CH/62/1
DocumentType
Draft
Pages
51
PublisherName
British Standards Institution
Status
Superseded
SupersededBy

IEC 60950-1:2005+AMD1:2009+AMD2:2013 CSV Information technology equipment - Safety - Part 1: General requirements
IEC 60038:2009 IEC standard voltages
IEC 60068-2-27:2008 Environmental testing - Part 2-27: Tests - Test Ea and guidance: Shock
EN 13718-1:2014 Medical vehicles and their equipment - Air ambulances - Part 1: Requirements for medical devices used in air ambulances
ISO 10651-2:2004 Lung ventilators for medical use Particular requirements for basic safety and essential performance Part 2: Home care ventilators for ventilator-dependent patients
MIL-STD-810 Revision G:2008 ENVIRONMENTAL ENGINEERING CONSIDERATIONS AND LABORATORY TESTS
IEC 60601-1:2005+AMD1:2012 CSV Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
IEC 60601-1-6:2010+AMD1:2013 CSV Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability
IEC 60721-3-7:1995+AMD1:1996 CSV Classification of environmental conditions - Part 3-7: Classification of groups of environmental parameters and their severities - Portable and non-stationary use
IEC 60601-1-8:2006+AMD1:2012 CSV Medical electrical equipment - Part 1-8: General requirements forbasic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems inmedical electrical equipment and medical electrical systems
IEC 60068-2-31:2008 Environmental testing - Part 2-31: Tests - Test Ec: Rough handling shocks, primarily for equipment-type specimens
IEC 60068-2-64:2008 Environmental testing - Part 2-64: Tests - Test Fh: Vibration, broadband random and guidance
IEC 60601-1-2:2014 Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests
ISO/TR 16142:2006 Medical devices Guidance on the selection of standards in support of recognized essential principles of safety and performance of medical devices
IEC 60529:1989+AMD1:1999+AMD2:2013 CSV Degrees of protection provided by enclosures (IP Code)
IEC TR 60721-4-7:2001+AMD1:2003 CSV Classification of environmental conditions - Part 4-7: Guidance for the correlation and transformation of environmental condition classes of IEC 60721-3 to the environmental tests of IEC 60068 - Portable and non-stationary use
IEC 61032:1997 Protection of persons and equipment by enclosures - Probes for verification

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