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IEC 60950-1:2005+AMD1:2009+AMD2:2013 CSV
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Information technology equipment - Safety - Part 1: General requirements |
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IEC 60038:2009
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IEC standard voltages |
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ISO 7010:2011
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Graphical symbols Safety colours and safety signs Registered safety signs |
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ASTM F 1452 : 2001
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Standard Specification for Minimum Performance and Safety Requirements for Anesthetic Gas Monitors |
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ISO 80601-2-13:2011
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Medical electrical equipment Part 2-13: Particular requirements for basic safety and essential performance of an anaesthetic workstation |
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ISO/TS 29041:2008
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Gas mixtures — Gravimetric preparation — Mastering correlations in composition |
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IEC 60068-2-27:2008
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Environmental testing - Part 2-27: Tests - Test Ea and guidance: Shock |
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EN 13718-1:2014
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Medical vehicles and their equipment - Air ambulances - Part 1: Requirements for medical devices used in air ambulances |
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ISO 10651-2:2004
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Lung ventilators for medical use Particular requirements for basic safety and essential performance Part 2: Home care ventilators for ventilator-dependent patients |
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MIL-STD-810 Revision G:2008
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ENVIRONMENTAL ENGINEERING CONSIDERATIONS AND LABORATORY TESTS |
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IEC 60601-1:2005+AMD1:2012 CSV
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Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
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EN 12598 : 1999
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OXYGEN MONITORS FOR PATIENT BREATHING MIXTURES - PARTICULAR REQUIREMENTS |
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IEC 60601-1-6:2010+AMD1:2013 CSV
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Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability |
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ISO 7767:1997
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Oxygen monitors for monitoring patient breathing mixtures — Safety requirements |
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IEC 60721-3-7:1995+AMD1:1996 CSV
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Classification of environmental conditions - Part 3-7: Classification of groups of environmental parameters and their severities - Portable and non-stationary use |
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IEC 60601-1-10:2007+AMD1:2013 CSV
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Medical electrical equipment - Part 1-10: General requirements forbasic safety and essential performance - Collateral Standard: Requirements for the development of physiologic closed-loopcontrollers |
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ISO 14937:2009
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Sterilization of health care products General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices |
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IEC 60601-1-8:2006+AMD1:2012 CSV
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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 |
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ISO 9918:1993
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Capnometers for use with humans Requirements |
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IEC 60068-2-31:2008
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Environmental testing - Part 2-31: Tests - Test Ec: Rough handling shocks, primarily for equipment-type specimens |
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IEC 60068-2-64:2008
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Environmental testing - Part 2-64: Tests - Test Fh: Vibration, broadband random and guidance |
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EN 864 : 1996
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MEDICAL ELECTRICAL EQUIPMENT - CAPNOMETERS FOR USE WITH HUMANS - PARTICULAR REQUIREMENTS |
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ISO 21647:2004
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Medical electrical equipment Particular requirements for the basic safety and essential performance of respiratory gas monitors |
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IEC 60601-1-2:2014
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Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests |
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ISO 6143:2001
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Gas analysis — Comparison methods for determining and checking the composition of calibration gas mixtures |
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ISO/TR 16142:2006
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Medical devices Guidance on the selection of standards in support of recognized essential principles of safety and performance of medical devices |
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ISO 14159:2002
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Safety of machinery — Hygiene requirements for the design of machinery |
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ISO 23328-2:2002
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Breathing system filters for anaesthetic and respiratory use — Part 2: Non-filtration aspects |
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IEC TR 60878:2015
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Graphical symbols for electrical equipment in medical practice |
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IEC 60529:1989+AMD1:1999+AMD2:2013 CSV
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Degrees of protection provided by enclosures (IP Code) |
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ISO 6142:2001
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Gas analysis Preparation of calibration gas mixtures Gravimetric method |
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IEC 60601-1-3:2008+AMD1:2013 CSV
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Medical electrical equipment - Part 1-3: General requirements forbasic safety and essential performance - Collateral Standard: Radiation protection in diagnostic X-ray equipment |
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IEC 61000-4-3:2006+AMD1:2007+AMD2:2010 CSV
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Electromagnetic compatibility (EMC) - Part 4-3: Testing and measurement techniques - Radiated, radio-frequency, electromagnetic field immunity test |
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ISO 80369-1:2010
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Small-bore connectors for liquids and gases in healthcare applications Part 1: General requirements |
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NFPA 53M : 1990
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FIRE HAZARDS IN OXYGEN-ENRICHED ATMOSPHERES |
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IEC TR 60721-4-7:2001+AMD1:2003 CSV
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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 |
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ISO 23328-1:2003
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Breathing system filters for anaesthetic and respiratory use — Part 1: Salt test method to assess filtration performance |
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ISO 14155:2011
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Clinical investigation of medical devices for human subjects Good clinical practice |
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ISO 14971:2007
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Medical devices Application of risk management to medical devices |
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ISO 7000:2014
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Graphical symbols for use on equipment Registered symbols |
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ISO 15223-1:2016
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Medical devices Symbols to be used with medical device labels, labelling and information to be supplied Part 1: General requirements |
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IEC 60601-1-9:2007+AMD1:2013 CSV
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Medical electrical equipment - Part 1-9: General requirements forbasic safety and essential performance - Collateral Standard: Requirements for environmentally conscious design |
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ISO 17664:2017
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Processing of health care products Information to be provided by the medical device manufacturer for the processing of medical devices |