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AAMI - 60601-2-25 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-25: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF ELECTROCARDIOGRAPHS Organization: AAMI
Date: 2011-01-01
Description: 1 The general standard is IEC 60601-1:2005, Medical electrical equipment – Part 1: General requirements for basic safety and essential performance.
IEEE - ANSI C63.18 - RECOMMENDED PRACTICE FOR AN ON-SITE, AD HOC TEST METHOD FOR ESTIMATING ELECTRIMAGNETIC IMMUNITY OF MEDICAL DEVICES TO RADIATED RADIO-FREQUENCY (RF) EMISSIONS FROM RF TRANSMITTERS Organization: IEEE
Date: 2014-01-01
Description: RF transmitters include two-way radios, walkie-talkies, mobile phones, wireless-enabled laptop computers and similar devices,1 RFID readers, networked mp3 players, two-way pagers, wireless PDAs, and wireless medical devices. The test protocol is designed to be performed as follows: a) By clinical engineers, biomedical engineers, and other technical personnel b) In a way that is relatively rapid and practical c) In an area and with equipment that are commonly available d) To identify specific effects and thresholds (i.e., transmit power and distance) to provide the basic information needed to develop a mitigation action plan e) To generate test results that can be used in the formulation of policies and procedures for managing the use of RF transmitters within a health-care facility A preferred method (5.6.2) and several alternative RF sources and methods (Annex C) for ad hoc testing are outlined in this recommended practice to allow flexibility with regard to the time, personnel, and resources available to perform the testing.
IEC 62103 - ELECTRONIC EQUIPMENT FOR USE IN POWER INSTALLATIONS - EDITION 1.0 Organization: IEC
Date: 2003-07-01
Description: This standard does not cover the following applications: Electrical accessories and electrical appliances for household and similar purposes, medical equipment, electric railway equipment, data processing without control on systems and processes, public and private non-industrial telecommunication and radio communication equipment and networks, protection relays, residual-current-operated protective devices, uninterruptible power supplies, lighting equipment and public charging equipment for electrical vehicles.
UL 61010-2-030 - UL STANDARD FOR SAFETY SAFETY REQUIREMENTS FOR ELECTRICAL EQUIPMENT FOR MEASUREMENT, CONTROL, AND LABORATORY USE – PART 2-030: PARTICULAR REQUIREMENTS FOR TESTING AND MEASURING CIRCUITS - FIRST EDITION; REPRINT WITH REVISIONS THROUGH AND INCLUDING SEPTEMBER 16, 2016 Organization: UL
Date: 2012-05-11
Description: Equipment excluded from scope This standard does not apply to equipment within the scope of: a) IEC 60065 (Audio, video and similar electronic apparatus); b) IEC 60204 (Safety of machinery – Electrical equipment of machines); c) IEC 60335 (Household and similar electrical appliances); d) IEC 60364 (Electrical installations of buildings); e) IEC 60439 (Low-voltage switchgear and controlgear assemblies); f) IEC 60601 (Medical electrical equipment); g) IEC 60950 (Information technology equipment including electrical business equipment, except as specified in 1.1.3); h) IEC 61558 (Power transformers, power supply units and similar); i) IEC 61010-031 (Hand-held probe assemblies); j) IEC 61243-3 (Live working – Voltage detectors – Part 3: Two-pole low-voltage type).
ETSI - EN 303 203-1 - ELECTROMAGNETIC COMPATIBILITY AND RADIO SPECTRUM MATTERS (ERM); SHORT RANGE DEVICES (SRD); MEDICAL BODY AREA NETWORK SYSTEMS (MBANSS) OPERATING IN THE 2 483,5 MHZ TO 2 500 MHZ RANGE; PART 1: TECHNICAL CHARACTERISTICS AND TEST METHODS - V1.1.1 Organization: ETSI
Date: 2014-11-01
Description: The present document covers the minimum characteristics of Medical Body Area Network System (MBANS), including the spectrum monitoring and access requirements, considered necessary in order to make the best use of the available spectrum within the 2 483,5 MHz to2 500 MHz frequency range and to avoid harmful interference between MBANS and other users of this band.
DSF/FPREN 60601-2-25 - MEDICAL ELECTRICAL EQUIPMENT -- PART 2-25: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF ELECTROCARDIOGRAPHS Organization: DS
Description: ME EQUIPMENT includes: a) direct-writing ELECTROCARDIOGRAPHS; b) other ME EQUIPMENT that produce ECG REPORTS for diagnostic purposes, e.g. patient monitors, defibrillators, exercise testing devices; c) ELECTROCARDIOGRAPHS having a display that is remote from the PATIENT (e.g. via phone lines, networks or storage media). These ME EQUIPMENT or ME SYSTEMS are within the scope of this particular standard excluding transmission media.
CEI - EN 60601-2-25 - MEDICAL ELECTRICAL EQUIPMENT PART 2: PARTICULAR REQUIREMENTS FOR BASIC SAFETY AND ESSENTIAL PERFORMANCE OF ELECTROCARDIOGRAPHS Organization: CEI
Date: 2016-04-01
Description: ME EQUIPMENT includes: a) direct-writing ELECTROCARDIOGRAPHS; b) other ME EQUIPMENT that produce ECG REPORTS for diagnostic purposes, e.g. patient monitors, defibrillators, exercise testing devices; c) ELECTROCARDIOGRAPHS having a display that is remote from the PATIENT (e.g. via phone lines, networks or storage media). These ME EQUIPMENT or ME SYSTEMS are within the scope of this particular standard excluding transmission media.
CSA C22.2 NO 60601-2-25 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-25: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF ELECTROCARDIOGRAPHS - SECOND EDITION Organization: CSA
Date: 2012-07-01
Description: ME EQUIPMENT includes: a) direct-writing ELECTROCARDIOGRAPHS; b) other ME EQUIPMENT that produce ECG REPORTS for diagnostic purposes, e.g. patient monitors, defibrillators, exercise testing devices; c) ELECTROCARDIOGRAPHS having a display that is remote from the PATIENT (e.g. via phone lines, networks or storage media). These ME EQUIPMENT or ME SYSTEMS are within the scope of this particular standard excluding transmission media.
IEC 60601-2-25 - MEDICAL ELECTRICAL EQUIPMENT – PART 2-25: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF ELECTROCARDIOGRAPHS - EDITION 2.0 Organization: IEC
Date: 2011-10-01
Description: ME EQUIPMENT includes: a) direct-writing ELECTROCARDIOGRAPHS; b) other ME EQUIPMENT that produce ECG REPORTS for diagnostic purposes, e.g. patient monitors, defibrillators, exercise testing devices; c) ELECTROCARDIOGRAPHS having a display that is remote from the PATIENT (e.g. via phone lines, networks or storage media). These ME EQUIPMENT or ME SYSTEMS are within the scope of this particular standard excluding transmission media.
CENELEC - EN 60601-2-25 - MEDICAL ELECTRICAL EQUIPMENT - PART 2-25: PARTICULAR REQUIREMENTS FOR THE BASIC SAFETY AND ESSENTIAL PERFORMANCE OF ELECTROCARDIOGRAPHS Organization: CENELEC
Date: 2015-10-01
Description: ME EQUIPMENT includes: a) direct-writing ELECTROCARDIOGRAPHS; b) other ME EQUIPMENT that produce ECG REPORTS for diagnostic purposes, e.g. patient monitors, defibrillators, exercise testing devices; c) ELECTROCARDIOGRAPHS having a display that is remote from the PATIENT (e.g. via phone lines, networks or storage media). These ME EQUIPMENT or ME SYSTEMS are within the scope of this particular standard excluding transmission media.
DS/EN 61558-2-15 - SAFETY OF TRANSFORMERS, REACTORS, POWER SUPPLY UNITS AND COMBINATIONS THEREOF - PART 2-15: PARTICULAR REQUIREMENTS AND TESTS FOR ISOLATING TRANSFORMERS FOR THE SUPPLY OF MEDICAL LOCATIONS Organization: DS
Date: 2012-03-23
Description: NOTE 4 Transformers covered by this standard are intended for the supply of medical locations. All other transformers or equipments connected downstream from the transformer are not covered by this Part 2.
CEI EN 61558-2-15 - SAFETY OF TRANSFORMERS, REACTORS, POWER SUPPLY UNITS AND COMBINATIONS THEREOF PART 2-15: PARTICULAR REQUIREMENTS AND TESTS FOR ISOLATING TRANSFORMERS FOR THE SUPPLY OF MEDICAL LOCATIONS Organization: CEI
Date: 2013-06-01
Description: NOTE 4 Transformers covered by this standard are intended for the supply of medical locations. All other transformers or equipments connected downstream from the transformer are not covered by this Part 2.
IEC 61558-2-15 - SAFETY OF TRANSFORMERS, REACTORS, POWER SUPPLY UNITS AND COMBINATIONS THEREOF – PART 2-15: PARTICULAR REQUIREMENTS AND TESTS FOR ISOLATING TRANSFORMERS FOR THE SUPPLY OF MEDICAL LOCATIONS - EDITION 2.0 Organization: IEC
Date: 2011-11-01
Description: NOTE 4 Transformers covered by this standard are intended for the supply of medical locations. All other transformers or equipments connected downstream from the transformer are not covered by this Part 2.
CENELEC - EN 61558-2-15 - SAFETY OF TRANSFORMERS, REACTORS, POWER SUPPLY UNITS AND COMBINATIONS THEREOF - PART 2-15: PARTICULAR REQUIREMENTS AND TESTS FOR ISOLATING TRANSFORMERS FOR THE SUPPLY OF MEDICAL LOCATIONS Organization: CENELEC
Date: 2012-02-01
Description: NOTE 4 Transformers covered by this standard are intended for the supply of medical locations. All other transformers or equipments connected downstream from the transformer are not covered by this Part 2.
SNZ - AS/NZS 61558.2.15 - SAFETY OF TRANSFORMERS, REACTORS POWER SUPPLY UNITS AND COMBINATIONS THEREOF – PART 2.15: PARTICULAR REQUIREMENTS AND TESTS FOR ISOLATING TRANSFORMERS FOR THE SUPPLY OF MEDICAL LOCATIONS Organization: SNZ
Date: 2012-10-26
Description: NOTE 4 Transformers covered by this standard are intended for the supply of medical locations. All other transformers or equipments connected downstream from the transformer are not covered by this Part 2.
ETSI - ES 200 674-1 - INTELLIGENT TRANSPORT SYSTEMS (ITS); ROAD TRANSPORT AND TRAFFIC TELEMATICS (RTTT); DEDICATED SHORT RANGE COMMUNICATIONS (DSRC); PART 1: TECHNICAL CHARACTERISTICS AND TEST METHODS FOR HIGH DATA RATE (HDR) DATA TRANSMISSION EQUIPMENT OPERATING IN THE 5,8 GHZ INDUSTRIAL, SCIENTIFIC AND MEDICAL (ISM) BAND - V2.4.1 Organization: ETSI
Date: 2012-08-01
Description: Additional standards or specifications may be required for equipment such as that intended for connection to the Public Switched Telephone Network (PSTN) or other systems.
ETSI - EN 300 674-3-1 - INTELLIGENT TRANSPORT SYSTEMS (ITS); ROAD TRANSPORT AND TRAFFIC TELEMATICS (RTTT); DEDICATED SHORT RANGE COMMUNICATIONS (DSRC); PART 3-1: TECHNICAL CHARACTERISTICS AND TEST METHODS FOR HIGH DATA RATE (HDR) DATA TRANSMISSION EQUIPMENT OPERATING IN THE 5,8 GHZ INDUSTRIAL, SCIENTIFIC AND MEDICAL (ISM) BAND - V3.0.0 Organization: ETSI
Date: 2010-06-01
Description: Additional standards or specifications may be required for equipment such as that intended for connection to the Public Switched Telephone Network (PSTN) or other systems.
CSA C22.3 NO 61936-1 - POWER INSTALLATIONS EXCEEDING 1 KV A.C. – PART 1: COMMON RULES - FIRST EDITION Organization: CSA
Date: 2008-01-01
Description: This standard does not apply to the design and erection of any of the following: – overhead and underground lines between separate installations; – electric railways (but not the substation feeding a railway system); – mining equipment and installations ; – fluorescent lamp installations; – installations on ships and off-shore installations; – electrostatic equipment; – test sites; – medical equipment, e.g. medical X-ray equipment. This standard does not apply to the design of factory-built, type-tested switchgear for which separate IEC standards exist.
IEC 61000-6-2 - ELECTROMAGNETIC COMPATIBILITY (EMC) - PART 6-2: GENERIC STANDARDS - IMMUNITY STANDARD FOR INDUSTRIAL ENVIRONMENTS - EDITION 3.0 Organization: IEC
Date: 2016-08-01
Description: NOTE 3 In special cases, situations will arise where the level of disturbances may exceed the levels specified in this standard, for example where equipment is installed in proximity to industrial, scientific and medical equipment as defined in CISPR 11 or where a hand-held transmitter is used in close proximity to equipment.
IEC 61000-6-2 REDLINE - ELECTROMAGNETIC COMPATIBILITY (EMC) - PART 6-2: GENERIC STANDARDS - IMMUNITY STANDARD FOR INDUSTRIAL ENVIRONMENTS - EDITION 3.0 Organization: IEC
Date: 2016-08-01
Description: NOTE 3 In special cases, situations will arise where the level of disturbances may exceed the levels specified in this standard, for example where equipment is installed in proximity to industrial, scientific and medical equipment as defined in CISPR 11 or where a hand-held transmitter is used in close proximity to an equipment.

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