IEC 60721-3-7:1995+AMD1:1996 CSV
Current
Current
The latest, up-to-date edition.
Classification of environmental conditions - Part 3-7: Classification of groups of environmental parameters and their severities - Portable and non-stationary use
Amended by
Available format(s)
Hardcopy , PDF , PDF 3 Users , PDF 5 Users , PDF 9 Users
Language(s)
English - French
Published date
10-24-2002
Publisher
FOREWORD
1 Scope
2 Normative references
3 Definitions
4 General
5 Classification of groups of environmental parameters
and their severities
6 Sets of environmental condition class combinations
Annex A (informative) Survey of conditions affecting the
choice of environmental parameters and their
severities
Annex B (informative) Interdependence of air temperature,
relative humidity and absolute humidity
Annex C (informative) Examples for practical application
of the classification specified in this standard
Annex D (informative) Summary of conditions covered by
sets of class combinations
Annex E (informative) Explanation of the environmental
conditions in tropical areas as specified in
classes 7K6 and 7K7
Tables
Figures
Classifies groups of environmental parameters and their severities to which products are subjected during portable and non-stationary use. This consolidated version consists of the second edition (1995) and its amendment 1 (1996). Therefore, no need to order amendment in addition to this publication.
| Committee |
TC 104
|
| DevelopmentNote |
Also numbered as BS EN 60721-3.7. (12/2005) Stability Date: 2021. (10/2017)
|
| DocumentType |
Standard
|
| Pages |
71
|
| PublisherName |
International Electrotechnical Committee
|
| Status |
Current
|
| Supersedes |
| Standards | Relationship |
| UNE-EN 60721-3-7:1997 | Identical |
| JIS C 0119:1999 | Identical |
| DIN EN 60721-3-7:1995-09 | Identical |
| NFC 20 000 : 90 AMD 1 93 | Identical |
| NF EN 60721 3-7 : 95 AMD 1 97 | Identical |
| NEN 10721-3-7 : 1995 AMD 1 1997 | Corresponds |
| I.S. EN 60721-3-7:1997 | Identical |
| PN EN 60721-3-7 : 2010 | Identical |
| SN EN 60721-3-7 : 1995 AMD 1 1997 | Identical |
| CEI 75-11 : 1ED 1990 | Identical |
| EN 60721-3-7:1995/A1:1997 | Identical |
| IS/IEC 60721 : Part 3 : Sec 7:2002 | Identical |
| BS 7527-3.7(1991) : 1991 AMD 7949 | Identical |
| JIS C 60721-3-7:1999 | Identical |
| BS EN ISO 20072:2013 | Aerosol drug delivery device design verification. Requirements and test methods |
| I.S. EN 60664-5:2007 | INSULATION COORDINATION FOR EQUIPMENT WITHIN LOW-VOLTAGE SYSTEMS - PART 5: COMPREHENSIVE METHOD FOR DETERMINING CLEARANCES AND CREEPAGE DISTANCES EQUAL TO OR LESS THAN 2 MM |
| UNI EN ISO 80601-2-61 : 2011 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-61: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF PULSE OXIMETER EQUIPMENT |
| I.S. EN 50491-2:2010 | GENERAL REQUIREMENTS FOR HOME AND BUILDING ELECTRONIC SYSTEMS (HBES) AND BUILDING AUTOMATION AND CONTROL SYSTEMS (BACS) - PART 2: ENVIRONMENTAL CONDITIONS |
| PREN ISO 80601-2-61 : DRAFT 2009 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-61: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF PULSE OXIMETER EQUIPMENT FOR MEDICAL USE |
| 09/30203808 DC : 0 | BS EN ISO 80601-2-12 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-12: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF CRITICAL CARE VENTILATORS |
| BS EN 60601-1-12:2015 | Medical electrical equipment General requirements for basic safety and essential performance. Collateral Standard: Requirements for medical electrical equipment and medical electrical systems intended for use in the emergency medical services environment |
| BS EN 60664-5:2003 | Insulation coordination for equipment within low-voltage systems A comprehensive method for determining clearances and creepage distances equal to or less than 2 mm |
| CEI EN 60051-1 : 1999 | DIRECT ACTING INDICATING ANALOGUE ELECTRICAL MEASURING INSTRUMENTS AND THEIR ACCESSORIES - PART 1: DEFINITIONS AND GENERAL REQUIREMENTS COMMON TO ALL PARTS |
| BS EN 61582:2006 | Radiation protection instrumentation. In vivo counters. Classification, general requirements and test procedures for portable, transportable and installed equipment |
| 96/211436 DC : DRAFT SEP 1996 | IEC 60721-3-0 - CLASSIFICATION OF ENVIRONMENTAL CONDITIONS - PART 3: CLASSIFICATION OF GROUPS OF ENVIRONMENTAL PARAMETERS AND THEIR SEVERITIES - SECTION 0: INTRODUCTION AND GUIDE |
| CSA Z9919 : 2007 : R2012 | MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF PULSE OXIMETER EQUIPMENT FOR MEDICAL USE |
| I.S. EN 62282-6-200:2017 | FUEL CELL TECHNOLOGIES - PART 6-200: MICRO FUEL CELL POWER SYSTEMS - PERFORMANCE TEST METHODS |
| PD IEC TR 63040:2016 | Guidance on clearances and creepage distances in particular for distances equal to or less than 2 mm. Test results of research on influencing parameters |
| BS EN ISO 80601-2-12:2011 | Medical electrical equipment Particular requirements for basic safety and essential performance of critical care ventilators |
| BS EN ISO 80601-2-61:2011 | Medical electrical equipment Particular requirements for basic safety and essential performance of pulse oximeter equipment |
| IEC TR 63040:2016 | Guidance on clearances and creepage distances in particular for distances equal to or less than 2 mm - Test results of research on influencing parameters |
| ISO 81060-1:2007 | Non-invasive sphygmomanometers — Part 1: Requirements and test methods for non-automated measurement type |
| EN 61582:2006 | Radiation protection instrumentation - In vivo counters - Classification, general requirements and test procedures for portable, transportable and installed equipment |
| DIN EN ISO 21649:2010-01 | Needle-free injectors for medical use - Requirements and test methods (ISO 21649:2006) |
| EN ISO 21647:2009 | Medical electrical equipment - Particular requirements for the basic safety and essential performance of respiratory gas monitors (ISO 21647:2004, including Cor 1:2005) |
| ONORM EN ISO 11608-4 : 2007 | PEN-INJECTORS FOR MEDICAL USE - PART 4: REQUIREMENTS AND TEST METHODS FOR ELECTRONIC AND ELECTROMECHANICAL PEN-INJECTORS |
| NF EN ISO 21649 : 2009 | NEEDLE-FREE INJECTORS FOR MEDICAL USE - REQUIREMENTS AND TEST METHODS |
| BS EN 60601-1-11:2015 | Medical electrical equipment 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 |
| BS EN 61709:2017 | Electric components. Reliability. Reference conditions for failure rates and stress models for conversion |
| BS EN ISO 80601-2-72:2015 | Medical electrical equipment Particular requirements for basic safety and essential performance of home healthcare environment ventilators for ventilator-dependent patients |
| NF EN 60664-5 : 2008 | INSULATION COORDINATION FOR EQUIPMENT WITHIN LOW-VOLTAGE SYSTEMS - PART 5: COMPREHENSIVE METHOD FOR DETERMINING CLEARANCES AND CREEPAGE DISTANCES EQUAL TO OR LESS THAN 2 MM |
| BS EN 60044-1:1999 | Instrument transformers Current transformers |
| 16/30309512 DC : 0 | BS EN 62327 ED 2.0 - RADIATION PROTECTION INSTRUMENTATION - HAND-HELD INSTRUMENTS FOR THE DETECTION AND IDENTIFICATION OF RADIONUCLIDES AND FOR THE ESTIMATION OF AMBIENT DOSE EQUIVALENT RATE FROM PHOTON RADIATION |
| 08/30168258 DC : 0 | BS IEC 62534 - RADIATION PROTECTION INSTRUMENTATION - HIGHLY SENSITIVE HAND-HELD INSTRUMENTS FOR NEUTRON DETECTION OF RADIOACTIVE MATERIAL |
| PD IEC TR 60721-4-7:2001 | Classification of environmental conditions. 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 |
| 11/30246729 DC : 0 | BS EN 62282-6-200 - FUEL CELL TECHNOLOGIES - PART 6-200: MICRO FUEL CELL POWER SYSTEMS - PERFORMANCE TEST METHODS |
| DIN EN ISO 80601-2-72:2016-04 | Medical electrical equipment - Part 2-72: Particular requirements for basic safety and essential performance of home healthcare environment ventilators for ventilator-dependent patients (ISO 80601-2-72:2015) |
| I.S. EN 60051-1:2017 | DIRECT ACTING INDICATING ANALOGUE ELECTRICAL MEASURING INSTRUMENTS AND THEIR ACCESSORIES - PART 1: DEFINITIONS AND GENERAL REQUIREMENTS COMMON TO ALL PARTS - PROPOSED HORIZONTAL STANDARD |
| UNI EN ISO 80601-2-12 : 2011 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-12: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF CRITICAL CARE VENTILATORS |
| BS ISO 81060-1 : 2007 COR 2012 | NON-INVASIVE SPHYGMOMANOMETERS - PART 1: REQUIREMENTS AND TEST METHODS FOR NON-AUTOMATED MEASUREMENT TYPE |
| 09/30181956 DC : DRAFT MAY 2009 | BS ISO 80601-2-61 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-61: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF PULSE OXIMETER EQUIPMENT FOR MEDICAL USE |
| CSA Z21647 : 2007 : R2012 : FR | MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RESPIRATORY GAS MONITORS |
| CAN/CSA-C22.2 NO. 80601-2-72:17 | Medical electrical equipment — Part 2-72: Particular requirements for basic safety and essential performance of home healthcare environment ventilators for ventilator-dependent patients (Adopted ISO 80601-2-72:2015, first edition, 2015-09-01, with Canadian deviations) |
| UNE-EN ISO 20072:2013 | Aerosol drug delivery device design verification - Requirements and test methods (ISO 20072:2009) |
| I.S. EN 62534:2015 | RADIATION PROTECTION INSTRUMENTATION - HIGHLY SENSITIVE HAND-HELD INSTRUMENTS FOR NEUTRON DETECTION OF RADIOACTIVE MATERIAL |
| UNI EN ISO 80601-2-55 : 2012 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-55: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RESPIRATORY GAS MONITORS |
| CSA C22.2 No. 80601-2-12 : 2012 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-12: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF CRITICAL CARE VENTILATORS |
| IEC 60051-1:2016 | Direct acting indicating analogue electrical measuring instruments and their accessories - Part 1: Definitions and general requirements common to all parts |
| IEC 80601-2-30:2018 | Medical electrical equipment - Part 2-30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers |
| DIN EN ISO 11608-4:2016-03 (Draft) | PEN-INJECTORS FOR MEDICAL USE - PART 4: REQUIREMENTS AND TEST METHODS FOR ELECTRONIC AND ELECTROMECHANICAL PEN-INJECTORS |
| I.S. EN ISO 21649:2009 | NEEDLE-FREE INJECTORS FOR MEDICAL USE - REQUIREMENTS AND TEST METHODS |
| CSA C22.2 No. 60601-1-11 : 2015 | 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 |
| UNI EN ISO 81060-1 : 2012 | NON-INVASIVE SPHYGMOMANOMETERS - PART 1: REQUIREMENTS AND TEST METHODS FOR NON-AUTOMATED MEASUREMENT TYPE |
| I.S. EN ISO 81060-1:2012 | NON-INVASIVE SPHYGMOMANOMETERS - PART 1: REQUIREMENTS AND TEST METHODS FOR NON-AUTOMATED MEASUREMENT TYPE (ISO 81060-1:2007) |
| 09/30197590 DC : 0 | BS EN ISO 80601-2-55 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-55: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RESPIRATORY GAS MONITORS |
| 16/30312315 DC : 0 | BS EN ISO 80601-2-55 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-55: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RESPIRATORY GAS MONITORS |
| 14/30296572 DC : 0 | BS EN 60601-1-11 - 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 |
| BS EN 62282-6-200:2012 | Fuel cell technologies Micro fuel cell power systems. Performance test methods |
| I.S. EN ISO 9919:2009 | MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF PULSE OXIMETER EQUIPMENT FOR MEDICAL USE |
| CEI EN 60664-5 : 2008 | INSULATION COORDINATION FOR EQUIPMENT WITHIN LOW-VOLTAGE SYSTEMS - PART 5: COMPREHENSIVE METHOD FOR DETERMINING CLEARANCES AND CREEPAGE DISTANCES EQUAL TO OR LESS THAN 2 MM |
| NF EN 61582 : 2006 | RADIATION PROTECTION INSTRUMENTATION - IN VIVO COUNTERS - CLASSIFICATION, GENERAL REQUIREMENTS AND TEST PROCEDURES FOR PORTABLE, TRANSPORTABLE AND INSTALLED EQUIPMENT |
| DIN EN ISO 80601-2-72 E : 2016 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-72: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF HOME HEALTHCARE ENVIRONMENT VENTILATORS FOR VENTILATOR-DEPENDENT PATIENTS (ISO 80601-2-72:2015) |
| I.S. EN 61709:2017 | ELECTRIC COMPONENTS - RELIABILITY - REFERENCE CONDITIONS FOR FAILURE RATES AND STRESS MODELS FOR CONVERSION |
| 96/216421 DC : DRAFT DEC 1996 | IEC 60721-3-10 - CLASSIFICATION OF ENVIRONMENTAL CONDITIONS - PART 3: CLASSIFICATION OF GROUPS OF ENVIRONMENTAL PARAMETERS AND THEIR SEVERITIES - SECTION 10: STATIONARY AND PORTABLE USE IN MINES |
| BS 7527-3.0(1991) : 1991 AMD 8009 | CLASSIFICATION ON ENVIRONMENTAL CONDITIONS - CLASSIFICATION OF ENVIRONMENTAL PARAMETERS AND THEIR SEVERITIES - INTRODUCTION |
| BS EN ISO 81060-1:2012 | Non-invasive sphygmomanometers Requirements and test methods for non-automated measurement type |
| BS IEC 62534 : 2010 | RADIATION PROTECTION INSTRUMENTATION - HIGHLY SENSITIVE HAND-HELD INSTRUMENTS FOR NEUTRON DETECTION OF RADIOACTIVE MATERIAL |
| 11/30244681 DC : 0 | BS IEC 62706 - RADIATION PROTECTION INSTRUMENTATION - ENVIRONMENTAL, ELECTROMAGNETIC AND MECHANICAL PERFORMANCE REQUIREMENTS |
| IEC 62327:2017 | Radiation protection instrumentation - Hand-held instruments for the detection and identification of radionuclides and for the estimation of ambient dose equivalent rate from photon radiation |
| UNE-EN 62282-6-200:2013 | Fuel cell technologies - Part 6-200: Micro fuel cell power systems - Performance test methods |
| AAMI ISO 81060-1:2007(R2013) | NON INVASIVE SPHYGMOMANOMETERS - PART 1: REQUIREMENTS AND TEST METHODS FOR NON-AUTOMATED MEASUREMENT TYPE |
| BS EN 62534:2015 | Radiation protection instrumentation. Highly sensitive hand-held instruments for neutron detection of radioactive material |
| UNI EN ISO 20072 : 2013 | AEROSOL DRUG DELIVERY DEVICE DESIGN VERIFICATION - REQUIREMENTS AND TEST METHODS |
| I.S. EN ISO 80601-2-12:2011 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-12: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF CRITICAL CARE VENTILATORS (ISO 80601-2-12:2011/COR 1:2011) |
| CSA Z9919 :2007 | MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF PULSE OXIMETER EQUIPMENT FOR MEDICAL USE |
| IEC 61709:2017 RLV | Electric components - Reliability - Reference conditions for failure rates and stress models for conversion |
| NF ETS 300019 1-7 : 1995 | TELECOMMUNICATIONS - INGENIERIE DES EQUIPEMENTS (EE) - CONDITIONS ET ESSAIS D'ENVIRONNEMENT DES EQUIPEMENTS DE TELECOMMUNICATIONS - PARTIE 1-7: CLASSIFICATION DES CONDITIONS D'ENVIRONNEMENT - UTILISATION EN DEPLACEMENT |
| I.S. EN 60601-1-12:2015 | MEDICAL ELECTRICAL EQUIPMENT - PART 1-12: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - COLLATERAL STANDARD: REQUIREMENTS FOR MEDICAL ELECTRICAL EQUIPMENT AND MEDICAL ELECTRICAL SYSTEMS INTENDED FOR USE IN THE EMERGENCY MEDICAL SERVICES ENVIRONMENT |
| EN ISO 80601-2-61:2011 | Medical electrical equipment - Part 2-61: Particular requirements for basic safety and essential performance of pulse oximeter equipment (ISO 80601-2-61:2011) |
| EN ISO 80601-2-55:2018 | Medical electrical equipment - Part 2-55: Particular requirements for the basic safety and essential performance of respiratory gas monitors (ISO 80601-2-55:2018) |
| EN 61709:2017 | Electric components - Reliability - Reference conditions for failure rates and stress models for conversion |
| IEC 60605-3-4:1992 | Equipment reliability testing - Part 3: Preferred test conditions - Section 4: Test cycle 4: Equipment for portable and non-stationary use - Low degree of simulation |
| IEC 61709 : 3.0 | ELECTRIC COMPONENTS - RELIABILITY - REFERENCE CONDITIONS FOR FAILURE RATES AND STRESS MODELS FOR CONVERSION |
| BS EN ISO 9919:2009 | Medical electrical equipment. Particular requirements for the basic safety and essential performance of pulse oximeter equipment for medical use |
| IEC 62282-6-200:2016 | Fuel cell technologies - Part 6-200: Micro fuel cell power systems - Performance test methods |
| BS EN ISO 21649:2009 | Needle-free injectors for medical use. Requirements and test methods |
| IEC 60044-1:1996+AMD1:2000+AMD2:2002 CSV | Instrument transformers - Part 1: Current transformers |
| IEC 60664-5:2007 | Insulation coordination for equipment within low-voltage systems - Part 5: Comprehensive method for determining clearances and creepage distances equal to or less than 2 mm |
| IEC 61582:2004 | Radiation protection instrumentation - In vivo counters - Classification, general requirements and test procedures for portable, transportable and installed equipment |
| ISO 21649:2006 | Needle-free injectors for medical use — Requirements and test methods |
| EN 60601-1-12:2015 | Medical electrical equipment - Part 1-12: General requirements for basic safety and essential performance - Collateral Standard: Requirements for medical electrical equipment and medical electrical systems intended for use in the emergency medical services environment |
| CSA C22.2 No. 80601-2-12 : 2012(R2017) | MEDICAL ELECTRICAL EQUIPMENT - PART 2-12: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF CRITICAL CARE VENTILATORS |
| UNI EN ISO 21647 : 2009 | MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RESPIRATORY GAS MONITORS |
| I.S. EN ISO 11608-4:2007 | PEN-INJECTORS FOR MEDICAL USE - PART 4: REQUIREMENTS AND TEST METHODS FOR ELECTRONIC AND ELECTROMECHANICAL PEN-INJECTORS |
| EN ISO 9919:2009 | Medical electrical equipment - Particular requirements for the basic safety and essential performance of pulse oximeter equipment for medical use (ISO 9919:2005) |
| UNI EN ISO 9919 : 2009 | MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF PULSE OXIMETER EQUIPMENT FOR MEDICAL USE |
| ANSI/AAMI HA60601-1-11:2015 | 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 |
| I.S. EN 61582:2006 | RADIATION PROTECTION INSTRUMENTATION - IN VIVO COUNTERS - CLASSIFICATION, GENERAL REQUIREMENTS AND TEST PROCEDURES FOR PORTABLE, TRANSPORTABLE AND INSTALLED EQUIPMENT |
| DIN EN ISO 20072:2013-10 | AEROSOL DRUG DELIVERY DEVICE DESIGN VERIFICATION - REQUIREMENTS AND TEST METHODS (ISO 20072:2009) |
| UNI EN ISO 21649 : 2009 | NEEDLE-FREE INJECTORS FOR MEDICAL USE - REQUIREMENTS AND TEST METHODS |
| AAMI ISO 81060-1 : 2007 | NON INVASIVE SPHYGMOMANOMETERS - PART 1: REQUIREMENTS AND TEST METHODS FOR NON-AUTOMATED MEASUREMENT TYPE |
| PD IEC/TR 60721-4-0:2002 | Classification of environmental conditions. Guidance for the correlation and transformation of environmental condition classes of IEC 60721-3 to the environmental tests of IEC 60068 Introduction |
| I.S. EN ISO 21647:2009 | MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RESPIRATORY GAS MONITORS |
| CEI EN 61582 : 2007 | RADIATION PROTECTION INSTRUMENTATION - IN VIVO COUNTERS - CLASSIFICATION, GENERAL REQUIREMENTS AND TEST PROCEDURES FOR PORTABLE, TRANSPORTABLE AND INSTALLED EQUIPMENT |
| 13/30264413 DC : 0 | BS EN ISO 80601-2-72 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-72: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF HOME HEALTHCARE ENVIRONMENT VENTILATORS FOR VENTILATOR-DEPENDENT PATIENTS |
| NF EN 60051-1 : 2017 | DIRECT ACTING INDICATING ANALOGUE ELECTRICAL MEASURING INSTRUMENTS AND THEIR ACCESSORIES - PART 1: DEFINITIONS AND GENERAL REQUIREMENTS COMMON TO ALL PARTS |
| IEC GUIDE 106:1996 | Guide for specifying environmental conditions for equipmentperformance rating |
| 12/30245174 DC : 0 | BS EN 60601-1-12 - MEDICAL ELECTRICAL EQUIPMENT - PART 1-12: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - COLLATERAL STANDARD: REQUIREMENTS FOR MEDICAL ELECTRICAL EQUIPMENT AND MEDICAL ELECTRICAL SYSTEMS INTENDED FOR USE IN THE EMERGENCY MEDICAL SERVICES ENVIRONMENT |
| 09/30155521 DC : 0 | 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 |
| CEI 56-20 : 2000 | EQUIPMENT RELIABILITY TESTING - PART 3: PREFERRED TEST CONDITIONS - SECTION 4: TEST CYCLE 4: EQUIPMENT FOR PORTABLE AND NON-STATIONARY USE - LOW DEGREE OF SIMULATION |
| PREN ISO 80601-2-55 : DRAFT 2009 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-55: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RESPIRATORY GAS MONITORS |
| 07/30145258 DC : 0 | BS ISO 20072 - AEROSOL DRUG DELIVERY DEVICES DESIGN VERIFICATION - REQUIREMENTS AND TEST METHODS |
| CSA Z21647:2007 | MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RESPIRATORY GAS MONITORS |
| CSA C60044-1 : 2007 : R2011 | INSTRUMENT TRANSFORMERS - PART 1: CURRENT TRANSFORMERS |
| CSA C60044-1 : 2007 | INSTRUMENT TRANSFORMERS - PART 1: CURRENT TRANSFORMERS |
| CEI EN 62282-6-200 : 2013 | FUEL CELL TECHNOLOGIES - PART 6-200: MICRO FUEL CELL POWER SYSTEMS - PERFORMANCE TEST METHODS |
| I.S. EN ISO 80601-2-72:2015 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-72: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF HOME HEALTHCARE ENVIRONMENT VENTILATORS FOR VENTILATOR-DEPENDENT PATIENTS (ISO 80601-2-72:2015) |
| I.S. EN 60601-1-11:2015 | 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 |
| CSA C22.2 No. 60601-1-12 : 2015 | MEDICAL ELECTRICAL EQUIPMENT - PART 1-12: GENERAL REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE - COLLATERAL STANDARD: REQUIREMENTS FOR MEDICAL ELECTRICAL EQUIPMENT AND MEDICAL ELECTRICAL SYSTEMS INTENDED FOR USE IN THE EMERGENCY MEDICAL SERVICES ENVIRONMENT |
| 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 61131-2:2017 | Industrial-process measurement and control - Programmable controllers - Part 2: Equipment requirements and tests |
| IEC TR 60721-4-0:2002 | Classification of environmental conditions - Part 4-0: Guidance for the correlation and transformation of the environmental condition classes of IEC 60721-3 to the environmental tests of IEC 60068 - Introduction |
| EN ISO 80601-2-12:2011/AC:2011 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-12: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF CRITICAL CARE VENTILATORS (ISO 80601-2-12:2011/COR 1:2011) |
| ISO 80601-2-12:2011 | Medical electrical equipment Part 2-12: Particular requirements for basic safety and essential performance of critical care ventilators |
| DIN EN ISO 21649 E : 2010 | NEEDLE-FREE INJECTORS FOR MEDICAL USE - REQUIREMENTS AND TEST METHODS |
| UNE-EN 50491-2:2011 | General requirements for Home and Building Electronic Systems (HBES) and Building Automation and Control Systems (BACS) -- Part 2: Environmental conditions |
| ISO 80601-2-72:2015 | Medical electrical equipment — Part 2-72: Particular requirements for basic safety and essential performance of home healthcare environment ventilators for ventilator-dependent patients |
| BS EN ISO 11608-4:2007 | Pen-injectors for medical use Requirements and test methods for electronic and electromechanical pen-injectors |
| ISO 20072:2009 | Aerosol drug delivery device design verification Requirements and test methods |
| ISO 11608-4:2006 | Pen-injectors for medical use Part 4: Requirements and test methods for electronic and electromechanical pen-injectors |
| ISO 21647:2004 | Medical electrical equipment Particular requirements for the basic safety and essential performance of respiratory gas monitors |
| IEC 62534:2010 | Radiation protection instrumentation - Highly sensitive hand-held instruments for neutron detection of radioactive material |
| BS EN 50491-2 : 2010 | GENERAL REQUIREMENTS FOR HOME AND BUILDING ELECTRONIC SYSTEMS (HBES) AND BUILDING AUTOMATION AND CONTROL SYSTEMS (BACS) - PART 2: ENVIRONMENTAL CONDITIONS |
| EN ISO 80601-2-72:2015 | Medical electrical equipment - Part 2-72: Particular requirements for basic safety and essential performance of home healthcare environment ventilators for ventilator-dependent patients (ISO 80601-2-72:2015) |
| EN ISO 21649:2009 | Needle-free injectors for medical use - Requirements and test methods (ISO 21649:2006) |
| IEC 80601-2-30:2018 RLV | Medical electrical equipment - Part 2-30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers |
| EN ISO 20072:2013 | Aerosol drug delivery device design verification - Requirements and test methods (ISO 20072:2009) |
| EN ISO 11608-4:2007 | Pen-injectors for medical use - Part 4: Requirements and test methods for electronic and electromechanical pen-injectors (ISO 11608-4:2006) |
| I.S. EN ISO 80601-2-61:2011 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-61: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF PULSE OXIMETER EQUIPMENT |
| DIN EN ISO 81060-1:2012-08 | Non-invasive sphygmomanometers - Part 1: Requirements and test methods for non-automated measurement type (ISO 81060-1:2007) |
| BS 5760-13.4:1993 | Reliability of systems, equipment and components. Guide to reliability test conditions for consumer equipment Conditions providing a low degree of simulation for equipment for portable and non-stationary use |
| BS IEC 62706:2012 | Radiation protection instrumentation. Environmental, electromagnetic and mechanical performance requirements |
| 16/30316718 DC : 0 | BS EN ISO 80601-2-61 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-61: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF PULSE OXIMETER EQUIPMENT |
| BS EN 60051-1:2017 | Direct acting indicating analogue electrical measuring instruments and their accessories Definitions and general requirements common to all parts |
| 15/30301708 DC : 0 | BS EN 62282-6-200 ED 3.0 - FUEL CELL TECHNOLOGIES - PART 6-200: MICRO FUEL CELL POWER SYSTEMS - PERFORMANCE TEST METHODS |
| 03/113382 DC : DRAFT SEP 2003 | BS EN ISO 21649 - NEEDLE-FREE INJECTORS FOR MEDICAL USE - REQUIREMENTS AND TEST METHODS |
| NF EN 300019 1-7 : 2004 | ENVIRONMENTAL ENGINEERING (EE) - ENVIRONMENTAL CONDITIONS AND ENVIRONMENTAL TESTS FOR TELECOMMUNICATIONS EQUIPMENT - PART 1-7: CLASSIFICATION OF ENVIRONMENTAL CONDITIONS - PORTABLE AND NO STATIONARY USE |
| IEC 80601-2-30 REDLINE : 2ED 2018 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-30: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF AUTOMATED NON-INVASIVE SPHYGMOMANOMETERS |
| CSA Z21647 : 2007 : R2012 | MEDICAL ELECTRICAL EQUIPMENT - PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RESPIRATORY GAS MONITORS |
| CSA C22.2 No. 80601-2-55 : 2014(R2019) | MEDICAL ELECTRICAL EQUIPMENT - PART 2-55: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RESPIRATORY GAS MONITORS |
| EN 60601-1-11:2015 | 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 |
| I.S. EN ISO 80601-2-55:2018 | MEDICAL ELECTRICAL EQUIPMENT - PART 2-55: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF RESPIRATORY GAS MONITORS (ISO 80601-2-55:2018) |
| ISO 80601-2-55:2018 | Medical electrical equipment — Part 2-55: Particular requirements for the basic safety and essential performance of respiratory gas monitors |
| CSA C22.2 No. 80601-2-61 : 2014(R2019) | MEDICAL ELECTRICAL EQUIPMENT - PART 2-61: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF PULSE OXIMETER EQUIPMENT |
| I.S. EN ISO 20072:2013 | AEROSOL DRUG DELIVERY DEVICE DESIGN VERIFICATION - REQUIREMENTS AND TEST METHODS (ISO 20072:2009) |
| BS EN ISO 21647:2009 | Medical electrical equipment. Particular requirements for the basic safety and essential performance of respiratory gas monitors |
| ISO 9919:2005 | Medical electrical equipment Particular requirements for the basic safety and essential performance of pulse oximeter equipment for medical use |
| EN ISO 81060-1:2012 | Non-invasive sphygmomanometers - Part 1: Requirements and test methods for non-automated measurement type (ISO 81060-1:2007) |
| EN 60044-1:1999/A2:2003 | INSTRUMENT TRANSFORMERS - PART 1: CURRENT TRANSFORMERS |
| EN 62534:2015 | Radiation protection instrumentation - Highly sensitive hand-held instruments for neutron detection of radioactive material |
| EN 60664-5:2007 | Insulation coordination for equipment within low-voltage systems - Part 5: Comprehensive method for determining clearances and creepage distances equal to or less than 2 mm |
| IEC 61709:2017 | Electric components - Reliability - Reference conditions for failure rates and stress models for conversion |
| EN 50491-2 : 2010 AMD 1 2015 | GENERAL REQUIREMENTS FOR HOME AND BUILDING ELECTRONIC SYSTEMS (HBES) AND BUILDING AUTOMATION AND CONTROL SYSTEMS (BACS) - PART 2: ENVIRONMENTAL CONDITIONS |
| EN 62282-6-200:2017 | Fuel cell technologies - Part 6-200: Micro fuel cell power systems - Performance test methods |
| EN 60051-1:2017 | Direct acting indicating analogue electrical measuring instruments and their accessories - Part 1: Definitions and general requirements common to all parts |
| IEC 60721-1:1990+AMD1:1992+AMD2:1995 CSV | Classification of environmental conditions - Part 1: Environmental parameters and their severities |
| IEC 60721-2-1:2013 | Classification of environmental conditions - Part 2-1: Environmental conditions appearing in nature - Temperature and humidity |
| IEC 60721-3-0:1984+AMD1:1987 CSV | Classification of environmental conditions - Part 3: Classification of groups of environmental parameters and their severities - Introduction |
| IEC 60721-3-2:1997 | Classification of environmental conditions - Part 3: Classification of groups of environmental parameters and their severities - Section 2: Transportation |
| IEC 60721-3-3:1994+AMD1:1995+AMD2:1996 CSV | Classification of environmental conditions - Part 3-3: Classification of groups of environmental parameters and their severities - Stationary use at weatherprotected locations |
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