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DS/IEC/TR 60788 - MEDICAL ELECTRICAL EQUIPMENT - GLOSSARY OF DEFINED TERMS Organization: DS
Date: 2004-07-27
Description: This Technical report comprises all defined terms used in the IEC standards and technical reports which -fall under the scope of MEDICAL ELECTRICAL EQUIPMENT, and -are on the list of publications as stated in May 2003.
DS/IEC/TR 62354 - GENERAL TESTING PROCEDURES FOR MEDICAL ELECTRICAL EQUIPMENT Organization: DS
Date: 2009-11-10
Description: This Technical Report applies to MEDICAL ELECTRICAL EQUIPMENT (as defined in Subclauses 3.63 of IEC 60601-1:2005 and 2.2.15 of IEC 60601-1:1988), hereinafter referred to as ME EQUIPMENT.
DSF/IEC TR 62354 - GENERAL TESTING PROCEDURES FOR MEDICAL ELECTRICAL EQUIPMENT Organization: DS
Description: This Technical Report applies to MEDICAL ELECTRICAL EQUIPMENT (as defined in Subclauses 3.63 of IEC 60601-1:2005 and 2.2.15 of IEC 60601-1:1988), hereinafter referred to as ME EQUIPMENT.
IEC/TR 60788 - MEDICAL ELECTRICAL EQUIPMENT GLOSSARY OF DEFINED TERMS - EDITION 2.0 Organization: IEC
Date: 2004-02-01
Description: This Technical report comprises all defined terms used in the IEC standards and technical reports which– fall under the scope of MEDICAL ELECTRICAL EQUIPMENT, and– are on the list of publications as stated in May 2003.
TSE - TS 4535 - SAFETY OF MEDICAL ELECTRICAL EQUIPMENTS GENERAL REQUIREMENTS Organization: TSE
Date: 1985-06-07
Description: This standard covers the general rules for safety of medical electrical equipments. Bu standard, hastahanelerde tıbbi araştırma merkezlerinde ve bu düzeydeki sağlık kuruluşlarında, uzman personel tarafından hasta çevresinde kullanılan veya denetlenen ve hasta ile ilgili olarak çevresindeki insan ve hayvanların can güvenliğini doğrudan etkileyen, elektrik enerjisi ile çalışan TIBBİ ELEKTRİKLİ CİHAZLAR için genel kuralları kapsr
DSF/IEC 62354 TR ED. 3 - 62A/936/CDTR - GENERAL TESTING PROCEDURES FOR MEDICAL ELECTRICAL EQUIPMENT Organization: DS
Description: This technical report applies to MEDICAL ELECTRICAL EQUIPMENT (as defined in Subclauses 3.63 of IEC 60601-1:2005 and 2.2.15 of IEC 60601-1:1988), hereinafter referred to as ME EQUIPMENT.
IEC TR 62354 - GENERAL TESTING PROCEDURES FOR MEDICAL ELECTRICAL EQUIPMENT - EDITION 3.0 Organization: IEC
Date: 2014-09-01
Description: This technical report applies to MEDICAL ELECTRICAL EQUIPMENT (as defined in Subclauses 3.63 of IEC 60601-1:2005 and 2.2.15 of IEC 60601-1:1988), hereinafter referred to as ME EQUIPMENT.
AAMI TIR62354 - GENERAL TESTING PROCEDURES FOR MEDICAL ELECTRICAL EQUIPMENT Organization: AAMI
Date: 2009-01-01
Description: Scope and object This technical report applies to MEDICAL ELECTRICAL EQUIPMENT (as defined in Subclauses 3.63 of IEC 60601-1:2005 and 2.2.15 of IEC 60601-1:1988), hereinafter referred to as ME EQUIPMENT.
IEC/TR 62354 - GENERAL TESTING PROCEDURES FOR MEDICAL ELECTRICAL EQUIPMENT - EDITION 2.0 Organization: IEC
Date: 2009-10-01
Description: Scope and object This technical report applies to MEDICAL ELECTRICAL EQUIPMENT (as defined in Subclauses 3.63 of IEC 60601-1:2005 and 2.2.15 of IEC 60601-1:1988), hereinafter referred to as ME EQUIPMENT.
DS/EN 62353 - MEDICAL ELECTRICAL EQUIPMENT - RECURRENT TEST AND TEST AFTER REPAIR OF MEDICAL ELECTRICAL EQUIPMENT Organization: DS
Date: 2014-11-14
Description: IEC 62353:2014 applies to testing of medical electrical equipment and medical electrical systems, hereafter referred to as ME equipment and ME systems, or parts of such equipment or systems, which comply with IEC 60601-1:1988 (second edition) and its amendments and IEC 60601-1:2005 (third edition) and its amendments, before putting into service, during maintenance, inspection, servicing and after repair or on occasion of recurrent tests to assess the safety of such ME equipment or ME systems or parts thereof.
IEC 62353 - MEDICAL ELECTRICAL EQUIPMENT – RECURRENT TEST AND TEST AFTER REPAIR OF MEDICAL ELECTRICAL EQUIPMENT - EDITION 2.0 Organization: IEC
Date: 2014-09-01
Description: This International Standard applies to testing of MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS, hereafter referred to as ME EQUIPMENT and ME SYSTEMS, or parts of such equipment or systems, which comply with IEC 60601-1:1988 (second edition) and its amendments and IEC 60601-1: 2005 (third edition) and its amendments, before PUTTING INTO SERVICE, during MAINTENANCE, INSPECTION, SERVICING and after REPAIR or on occasion of RECURRENT TESTS to assess the safety of such ME EQUIPMENT or ME SYSTEMS or parts thereof.
CENELEC - EN 62353 - MEDICAL ELECTRICAL EQUIPMENT - RECURRENT TEST AND TEST AFTER REPAIR OF MEDICAL ELECTRICAL EQUIPMENT Organization: CENELEC
Date: 2014-10-01
Description: This International Standard applies to testing of MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS, hereafter referred to as ME EQUIPMENT and ME SYSTEMS, or parts of such equipment or systems, which comply with IEC 60601-1:1988 (second edition) and its amendments and IEC 60601-1: 2005 (third edition) and its amendments, before PUTTING INTO SERVICE, during MAINTENANCE, INSPECTION, SERVICING and after REPAIR or on occasion of RECURRENT TESTS to assess the safety of such ME EQUIPMENT or ME SYSTEMS or parts thereof.
CEI EN 62353 - MEDICAL ELECTRICAL EQUIPMENT - RECURRENT TEST AND TEST AFTER REPAIR OF MEDICAL ELECTRICAL EQUIPMENT Organization: CEI
Date: 2015-11-01
Description: This International Standard applies to testing of MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS, hereafter referred to as ME EQUIPMENT and ME SYSTEMS, or parts of such equipment or systems, which comply with IEC 60601-1:1988 (second edition) and its amendments and IEC 60601-1:2005 (third edition) and its amendments, before PUTTING INTO SERVICE, during MAINTENANCE, INSPECTION, SERVICING and after REPAIR or on occasion of RECURRENT TESTS to assess the safety of such ME EQUIPMENT or ME SYSTEMS or parts thereof.
SNV - SN EN 62353 - MEDICAL ELECTRICAL EQUIPMENT - RECURRENT TEST AND TEST AFTER REPAIR OF MEDICAL ELECTRICAL EQUIPMENT Organization: SNV
Date: 2008-01-01
Description: Foreword The text of document 62A/564/FDIS, future edition 1 of IEC 62353, prepared by SC 62A, Common aspects of electrical equipment used in medical practice, of IEC TC 62, Electrical equipment in medical practice, was submitted to the IEC-CENELEC parallel vote and was approved by CENELEC as EN 62353 on 2007-09-11.
IEC TR 60601-4-2 - MEDICAL ELECTRICAL EQUIPMENT – PART 4-2: GUIDANCE AND INTERPRETATION – ELECTROMAGNETIC IMMUNITY: PERFORMANCE OF MEDICAL ELECTRICAL EQUIPMENT AND MEDICAL ELECTRICAL SYSTEMS - EDITION 1.0 Organization: IEC
Date: 2016-05-01
Description: Hereafter, MEDICAL ELECTRICAL EQUIPMENT or a MEDICAL ELECTRICAL SYSTEM are referred to as ME EQUIPMENT or an ME SYSTEM.
IEC/TR 60513 - FUNDAMENTAL ASPECTS OF SAFETY STANDARDS FOR MEDICAL ELECTRICAL EQUIPMENT - EDITION 2.0 Organization: IEC
Date: 1994-01-01
Description: This report is primarily intended to be used by:- those who prepare standards for the design, installation and use of medical electrical equipment;- health care regulatory authorities, test houses and other organizations responsible for implementing standards for medical electrical equipment;- manufacturers of medical electrical equipment;- those who assemble systems which include medical electrical equipment.
IEC/TR 62266 - MEDICAL ELECTRICAL EQUIPMENT - GUIDELINES FOR IMPLEMENTATION OF DICOM RADIOTHERAPY - EDITION 1.0 Organization: IEC
Date: 2002-03-01
Description: Ultimately, a decision was made by the IEC to adopt four DICOM RT objects as an IEC standard which appeared in April 1998 as IEC 61852 ‘Medical Electrical Equipment – Digital Imaging and Communication System in Medicine (DICOM) – Radiotherapy Objects First Edition'.
DS/EN 62274 - MEDICAL ELECTRICAL EQUIPMENT - SAFETY OF RADIOTHERAPY RECORD AND VERIFY SYSTEMS Organization: DS
Date: 2005-07-15
Description: This International Standard applies to the design and manufacture and some installation aspects of a record and verify system (RVS) for use in radiotherapy in human medical practice that a) provides, defines, or displays treatment machine set up data; imports data either through input by the operator or directly from other devices, b) may control the ability of that equipment to operate; c) records data of all treatment sessions; and d) is intended to be: 1) for normal use, under the authority of appropriately licensed or qualified persons, by operators having the required skills and training; 2) maintained in accordance with the recommendations given in the instructions for use; and 3) used within the environmental and electrical supply conditions specified in the technical description.
IEC 62274 - MEDICAL ELECTRICAL EQUIPMENT SAFETY OF RADIOTHERAPY RECORD AND VERIFY SYSTEMS - EDITION 1.0 Organization: IEC
Date: 2005-05-01
Description: This International Standard applies to the design and manufacture and some installation aspects of a RECORD AND VERIFY SYSTEM (RVS) for use in RADIOTHERAPY in human medical practice that a) provides, defines, or displays treatment machine set up data; imports data either through input by the OPERATOR or directly from other devices, b) may control the ability of that equipment to operate; c) records data of all TREATMENT sessions; and d) is intended to be: 1) for NORMAL USE, under the authority of appropriately licensed or QUALIFIED PERSONS, by OPERATORS having the required skills and training; 2) maintained in accordance with the recommendations given in the INSTRUCTIONS FOR USE; and 3) used within the environmental and electrical supply conditions specified in the technical description.
DSF/IEC/TR 60601-4-2 - IEC TR 60601-4-2: MEDICAL ELECTRICAL EQUIPMENT - PART 4-2: GUIDANCE AND INTERPRETATION - ELECTROMAGNETIC IMMUNITY; PERFORMANCE OF MEDICAL ELECTRICAL EQUIPMENT AND MEDICAL ELECTRICAL SYSTEMS Organization: DS
Description: Hereafter, MEDICAL ELECTRICAL EQUIPMENT or a MEDICAL ELECTRICAL SYSTEM are referred to as ME EQUIPMENT or an ME SYSTEM.

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