IEC - International Electrotechnical Commission Datasheets for Standards and Technical Documents
Standards and technical documents includes standards, codes, regulation, handbooks, manuals, comprehensive guides and other formal publications. Standards, codes, and regulation establish uniform specifications, procedures or technical criteria.
Standards and Technical Documents: Learn more
| Product Name | Notes |
|---|---|
| A 15% discount of the total catalogue price is included. This pack contains the following: IEC 60601-1:2005+AMD1:20 12+AMD2:2020 CSV IEC 60601-1-2:2014+AMD1: 2020 CSV IEC 60601-1-3:2008+AMD1: 2013+AMD2:2021 CSV IEC 60601-1-6:2010+AMD1: 2013+AMD2:2020... | |
| Amends the standard IEC 60601-2-19 to reflect IEC 60601-1 2nd edition with its amendments 1 (1991) and 2 (1995). Contains new subclauses. | |
| Amends the standard IEC 60601-2-20 to reflect IEC 60601-1 second edition with its amendments 1 (1991) and 2 (1995). Contains new subclauses. | |
| Amends the standard IEC 60601-2-21 to reflect IEC 60601-1 second edition with its amendments 1 (1991) and 2 (1995). Contains new subclauses. | |
| Applies to a group of related rectangular, multicontact, two-part printed board connectors with male and female contacts in conjunction with either solder or solderless terminations (such as wrap type). All... | |
| Applies to a group of related two-part connectors for printed boards for board-to-board and board-to-wire connection, with tin or gold plated contact area according to the style. The free or... | |
| Applies to circular connectors for low-frequency audio and video applications such as audio, video and audio-visual equipment. Specifies dimensions, general requirements and tests. | |
| Applies to direct blood-pressure monitoring equipment. Establishes particular requirements for the safety of that equipment and the electrical safety requirements for catheter tip transducers. Does not apply to catheter tubing,... | |
| Applies to direct current (d.c.) powered mobile equipment. The equipment is operated while being transported, for example in or on a vehicle but does not form part of the vehicle,... | |
| Applies to equipment and devices associated to X-ray equipment as used for supporting and relatively positioning the functional components including the patient support used for the application of the X-radiation. | |
| Applies to equipment for stationary use in weatherprotected locations and in temperate climates. Contains preferred test conditions given in IEC 605-1. | |
| Applies to equipment installed in partially weather-protected locations in a climate belonging to the group of 'moderate' climates covered by IEC 60721-2-1. Contains preferred test conditions as referred to in... | |
| Applies to high-voltage generators of medical diagnostic X-ray generators and to their subassemblies including the following : - high-voltage generators that are integrated with an X-ray tube assembly; - high-voltage... | |
| Applies to indoor portable equipment operated in a stationary position with a low degree of simulation. Contains preferred test conditions given in IEC 605-1. | |
| Applies to laser equipment for medical application, classified as a class 3B or class 4 laser product according to IEC 825. It deals with the particular requirements for the safety... | |
| Applies to laser equipment for medical applications, classified as a class 3B or class 4 laser product according to the classification in IEC 60825-1. | |
| Applies to magnetic video recording and/or reproducing using 25.4 mm (1 in) tape on type B helical-scan recorders suitable for broadcast applications. Defines the electrical and mechanical characteristics of equipment... | |
| Applies to medical equipment, medical electrical systems, information technology equipment used in medical electrical application, and all other equipment forming part of medical electrical systems. Specifies general requirements and tests... | |
| Applies to outdoor transportable equipment operating only while in a stationary position in a climate belonging to the group of climates described as "warm temperate" in IEC 60721-2-1. The degree... | |
| Applies to power transformers complying with IEC 76. Object is to assist purchasers in the determination and selection of transformer characteristics at the time of purchase and subsequent usage. Comprises... | |
| Applies to radiotherapy simulators which use diagnostic X-ray equipment to simulate physically a therapeutic radiation beam, so that the treatment volume to be irradiated during radiotherapy can be localized and... | |
| Applies to radiotherapy simulators: - that use diagnostic X-ray equipment to simulate physically a therapeutic radiation beam, so that the treatment volume to be subjected to irradiation during radiotherapy can... | |
| Applies to the basic safety and essential performance of peritoneal dialysis medical electrical equipment. It applies to peritoneal dialysis equipment intended for use either by medical staff or under the... | |
| Applies to the basic safety and essential performance of ultrasonic diagnostic equipment. The approach and philosophy used in drafting this particular standard for safety of ultrasonic diagnostic equipment are consistent... | |
| Applies to the safety and essential performance of laser equipment for either surgical, therapeutic, medical diagnostic, cosmetic, or veterinary applications, intended for its use on humans or animals, classified as... | |
| Applies to the safety of equipment for extracorporeally induced lithotripsy, i.e. device for treatment with extracorporeally generated pressure pulses. The applicability of this standard is limited to components directly involved... | |
| Applies to the safety of medical electrical systems, as defined as follows: combination of items of equipment, at least one of which must be medical electrical equipment and inter-connected by... | |
| Applies to therapeutic X-ray equipment with nominal X-ray tube voltages in the range 10 kV to 1 MV when connected to alternating current supply mains. Establishes requirements for the safety... | |
| Applies to X-ray equipment for computed tomography (CT scanners). Includes safety requirements for the X-ray generator, and those where high voltage generators are integrated with an X-ray tube assembly. Specify... | |
| Contains a series of revisions to IEC 60601-2-3 (second edition, 1991) taking into account amendments 1 and 2 of the General Standard, which include reference to the collateral standards. | |
| Contains modifications to IEC 601-2-17 in order to adapt this standard to IEC 601-1 second edition (1988). | |
| Contains test procedures, classified into three grades, for compliance with the radiation safety requirements of IEC 601-2-11. | |
| Covers 8 way connectors, up to 4 pairs, and specifies mechanical and environmental requirements, and electrical transmission requirements for frequencies up to 600 MHz. These connectors are typically used as... | |
| Covers 8 way connectors, up to 4 pairs, to be used up to 600 MHz, when used with an appropriate cable. These cables are specified in the IEC 61156 series... | |
| Covers 8-way shielded free and fixed connectors and specifies mechanical and environmental requirements and electrical transmission requirements for frequencies up to 100 MHz. These connectors are typically used as category... | |
| Covers 8-way unshielded free and fixed connectors and specifies mechanical and environmental requirements and electrical transmission requirements for frequencies up to 250 MHz. These connectors are typically used as category... | |
| Covers 8-way, unshielded, free and fixed connectors, and specifies mechanical and environmental requirements, and electrical transmission requirements for frequencies up to 100 MHz. These connectors are typically used as category... | |
| Covers a group of related two-part connectors for printed boards and cable connectors associated with printed backpanels. The group covers high-density connectors having up to 96 miniature contacts for low-voltage... | |
| Covers a range of connectors with 2.54 mm (0.1 in) contact spacing intended to connect a single or double-sided printed board to another printed board or wires. Two kinds are... | |
| Covers a range of connectors with 2.54 mm (0.1 in) spacing intended to connect a double-sided printed board to another printed board or wires. Two kinds of connector are available:... | |
| Covers a range of two-part connectors with contact arrangements having spacings of 2,54 mm (0,1 in) in both directions. | |
| Covers an 8-way connector system of 4, 6 or 8 contacts consisting of a range of free and fixed connectors. The connectors cover a variety of different mounting configurations and... | |
| Covers concentric connectors for use in LF (low-frequency) audio applications such as the interconnection of headphones and microphones in sound system components. Specifies the dimensions, general requirements and tests for... | |
| Covers dimensions, general requirements and tests for a range of sockets designed for use with integrated circuits in dual-in-line format. Sockets include standard type and low-profile type. | |
| Describes a group of related two-part connectors for printed boards, with 32, 48, 64 and 96 contacts for low-voltage applications. | |
| Describes how the concentrations of dissolved gases or free gases may be interpreted to diagnose the condition of a transformer in service and suggests corrective actions. May also apply in... | |
| Describes how the concentrations of dissolved gases or free gases may be interpreted to diagnose the condition of oil-filled electrical equipment in service and suggests future action. Applicable to electrical... | |
| Electroconvulsive therapy equipment for the treatment of psychiatric disorders is intended for use by or under the supervision of qualified personnel in a medical environment. It may, nevertheless, introduce hazards... | |
| Establishes general requirements for protection against ionizing radiation in medical diagnostic X-ray equipment, in order that the dose equivalent to the patient, the operator and other staff can be kept... | |
| Establishes limits for dimensions and other physical characteristics necessary to ensure interchangeability of 'Topflash/ Flipflash' array. | |
| Establishes mandatory requirements and gives a list of characteristics of equipment for grading and sorting radioactive ores in containers at minehead and in opencast workings. | |
| Establishes particular requirements for the safety of electromyographs and evoked response equipment as defined in clause 2 of this standard. | |
| Establishes particular requirements for the safety of endoscopic equipment and enables parts of endoscopic equipment to be tested together or individually. | |
| Establishes particular requirements for the safety of surgical luminaires and luminaires for diagnosis. | |
| Establishes particular requirements for the safety of ultrasonic diagnostic equipment and those aspects thereof which are directly related to safety. Does not cover ultrasonic therapeutic equipment; however, equipment used for... | |
| Establishes particular requirements for the safety, including the essential performance of invasive blood pressure monitoring and measuring equipment. This particular standard takes into account Collateral Standard 60601-1-2:(1993) Electromagnetic compatibility and... | |
| Establishes particular requirements, in addition to the requirements of IEC 60601-2-25, for the safety, including essential performance of recording and analysing single channel and multichannel electrocardiographs. These requirements shall apply... | |
| Establishes requirements applying to capacitor discharge X-ray generators for medical radiology in which electrical energy for loading of the X-ray tube is primarily stored at and switched in the high-voltage... | |
| Establishes requirements for a satisfactory level of radiation safety and of electrical and mechanical safety for gamma beam radiotherapy equipment used in medicine. | |
| Establishes requirements for a satisfactory level of radiation safety for medical electron accelerators used in human medical practice for therapy under the jurisdiction of a qualified person. Applies to accelerators... | |
| Establishes requirements for safe operation of X-ray equipment for computed tomography (CT scanners). | |
| Establishes requirements for the safety of magnetic resonance equipment to provide protection for the patient, the operator, staff associated with magnetic resonance equipment and the general public. It also provides... | |
| Establishes requirements for the safety of magnetic resonance equipment to provide protection for the patient. It establishes requirements to provide information to the operator, staff associated with magnetic resonance equipment... | |
| Establishes requirements to be complied with by manufacturers in the design and construction of electron accelerators for use in radiotherapy and defines type tests and site tests. Places limits on... | |
| Establishes requirements, which minimize hazards to patient and operator, for heating devices such as blankets, pads, mattresses and fluid-filled mattresses. Specifies tests by which comliance can be verified. | |
| Establishes safety requirements for the design and manufacture of X-ray equipment for prolonged radioscopically guided interventional procedures. Specifies information which is to be provided with such equipment for the assistance... | |
| features Applies to groups of related two-part connectors for use with printed boards. They range from connectors with high contact density for low-voltage applications to connectors for heavy currents and... | |
| Following on the general requirements of IEC 601-1 for the safety of electromedical equipment, this standard specifies safety requirements for medical anaesthetic machines that incorporate electrical components, lung ventilators and... | |
| Formulates appropriate design and manufacturing requirements for the safety of mammographic X-ray equipment and mammographic stereotactic devices, reflecting the particular characteristics and circumstances of use of such equipment. | |
| Gives brief diagrammatic guidance to the test specification writer and the test engineer on how to use IEC 605 in preparing for, executing, and interpreting equipment reliability tests. | |
| Gives data for generally applicable interconnection between video tape recorders and television receivers for 50 Hz-625 line systems. Provides contact arrangement and contact destination for the circular socket connector 130-9... | |
| Gives numerical methods for testing the statistical validity of the constant failure rate assumption, underlying the methods given in IEC 605-4 and 605-7. Gives recommendations for action if the assumption... | |
| Gives recommendations for specification reliability requirements for compliance testing, selection of test conditions for reliability tests, preparation of detailed reliability test specifications, evaluation of information from reliability testing and writing... | |
| Gives recommended numerical and graphical methods for determining point estimates and confidence limits of reliability characteristics from equipment reliability determination tests. The methods of calculation may be applied at any... | |
| Gives specifications of pliable conduits of insulating material and should not be used without IEC 614-1. | |
| Gives the statistical test plans which are valid for reliability compliance tests concerning failure rate, mean time between failures and mean time to failure. Should be used in conjunction with... | |
| Haemodialysis is a highly specialized treatment to correct the electrolytes and imbalances in a patient's blood by means of diffusion and/or ultrafiltration. It necessitates delicate haemodialysis equipment for which this... | |
| IEC 60598-2-8:2013 specifies requirements for handlamps and similar portable luminaires which are held in the hand, hooked up or resting on a surface for use with electric light sources on... | |
| IEC 60599:2015 describes how the concentrations of dissolved gases or free gases may be interpreted to diagnose the condition of oil-filled electrical equipment in service and suggest future action. This... | |
| IEC 60599:2015 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy... | |
| IEC 60599:2022 CMV contains both the official standard and its commented version. The commented version provides you with a quick and easy way to compare all the changes between IEC... | |
| IEC 60599:2022 describes how the concentrations of dissolved gases or free gases can be interpreted to diagnose the condition of oil-filled electrical equipment in service and suggest future action. This... | |
| IEC 60601-1-10:2007+A1:2 013 Specifies requirements for the development (analysis, design, verification and validation) of a physiologic closed-loop controller (PCLC) as part of a physiologic closed-loop control system (PCLCS) in medical... | |
| IEC 60601-1-10:2007+A1:2 013+A2:2020 Specifies requirements for the development (analysis, design, verification and validation) of a physiologic closed-loop controller (PCLC) as part of a physiologic closed-loop control system (PCLCS) in medical... | |
| IEC 60601-1-11:2010 applies to the basic safety and essential performance of medical electrical equipment and medical electrical systems which are intended by their manufacturer for use in the home healthcare... | |
| IEC 60601-1-11:2015 applies to the basic safety and essential performance of medical electrical equipment and medical electrical systems for use in the home healthcare environment. It applies regardless of whether... | |
| IEC 60601-1-11:2015 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy... | |
| IEC 60601-1-11:2015+A1:2 020 applies to the basic safety and essential performance of medical electrical equipment and medical electrical systems for use in the home healthcare environment. It applies regardless of... | |
| IEC 60601-1-12:2014 constitutes a collateral standard to IEC 60601-1: Medical electrical equipment - Part 1: General requirements for basic safety and essential performance hereafter referred to as the general standard. | |
| IEC 60601-1-12:2014+A1:2 020 constitutes a collateral standard to IEC 60601-1: Medical electrical equipment - Part 1: General requirements for basic safety and essential performance hereafter referred to as the general... | |
| IEC 60601-1-2:2014 applies to the basic safety and essential performance of Medical Equipment (ME) equipment and ME systems in the presence of electromagnetic disturbances and to electromagnetic disturbances emitted by... | |
| IEC 60601-1-2:2014+A1:20 20 applies to the basic safety and essential performance of Medical Equipment (ME) equipment and ME systems in the presence of electromagnetic disturbances and to electromagnetic disturbances emitted... | |
| IEC 60601-1-3:2008+A1:20 13 applies to X-ray equipment and to subassemblies of such equipment, where radiological images of a human patient are used for diagnosis, planning or guidance of medical procedures. | |
| IEC 60601-1-3:2008+A1:20 13+A2:2021 applies to X-ray equipment and to subassemblies of such equipment, where radiological images of a human patient are used for diagnosis, planning or guidance of medical procedures. | |
| IEC 60601-1-6:2010 specifies a process for a manufacturer to analyse, specify, design, verify and validate usability, as it relates to basic safety and essential performance of medical electrical equipment. This... | |
| IEC 60601-1-6:2010+A1:20 13 specifies a process for a manufacturer toanalyse, specify, design, verify and validate usability, as it relates to basic safety and essential performance of medical electrical equipment. This... | |
| IEC 60601-1-6:2010+A1:20 13+A2:2020 specifies a process for a manufacturer toanalyse, specify, design, verify and validate usability, as it relates to basic safety and essential performance of medical electrical equipment. This... | |
| IEC 60601-1-8:2006+A1:20 12 Specifies basic safety and essential performance requirements and tests for alarm systems in medical electrical equipment and medical electrical systems and to provide guidance for their application. | |
| IEC 60601-1-8:2006+A1:20 12+A2:2020 Specifies basic safety and essential performance requirements and tests for alarm systems in medical electrical equipment and medical electrical systems and to provide guidance for their application. | |
| IEC 60601-1-9:2007 The objective of this collateral standard is to improve the environmental impact for the entire range of medical electrical equipment, taking into account all stages of the product... | |
| IEC 60601-1-9:2007+A1:20 13 The objective of this collateral standard is to improve the environmental impact for the entire range of medical electrical equipment, taking into account all stages of the... | |
| IEC 60601-1-9:2007+A1:20 13+A2:2020 The objective of this collateral standard is to improve the environmental impact for the entire range of medical electrical equipment, taking into account all stages of the... | |
| IEC 60601-1:2005 contains requirements concerning basic safety and essential performance that are generally applicable to medical electrical equipment. For certain types of medical electrical equipment, these requirements are either supplemented... | |
| IEC 60601-1:2005+A1:2012 contains requirements concerning basic safety and essential performance that are generally applicable to medical electrical equipment. For certain types of medical electrical equipment, these requirements are either supplemented... | |
| IEC 60601-1:2005+A1:2012 +A2:2020 contains requirements concerning basic safety and essential performance that are generally applicable to medical electrical equipment. For certain types of medical electrical equipment, these requirements are either... | |
| IEC 60601-2-10:2012 specifies the requirements for the safety and essential performance of nerve and muscle stimulators, for use in the practice of physical medicine. This includes transcutaneous electrical nerve stimulators... | |
| IEC 60601-2-10:2012+A1:2 016 specifies the requirements for the safety and essential performance of nerve and muscle stimulators, for use in the practice of physical medicine. This includes transcutaneous electrical nerve... | |
| IEC 60601-2-10:2012+AMD1 :2016+AMD2:2023 CSV specifies the requirements for the safety and essential performance of nerve and muscle stimulators, for use in the practice of physical medicine. This includes transcutaneous electrical... | |
| IEC 60601-2-11:2013 applies to the basic safety and essential performance of gamma beam therapy equipment, including multi-source stereotactic radiotherapy equipment. This particular standard of the 60601 series, establishes requirements to... | |
| IEC 60601-2-13:2003+A1:2 006(E) specifies particular safety and essential performance requirements for individual devices designed for use in an anaesthetic system as well as specific requirements for the anaesthetic gas delivery... | |
| IEC 60601-2-16:2008 applies to the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment. IEC 60601-2-16:2008 does not take into consideration the dialysing fluid control system of Haemodialysis... | |
| IEC 60601-2-16:2012 applies to the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment. IEC 60601-2-16:2012 does not take into consideration the dialysis fluid control system of Haemodialysis... | |
| IEC 60601-2-16:2018 applies to the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment. IEC 60601-2-16:2018 does not take into consideration the dialysis fluid control system of Haemodialysis... | |
| IEC 60601-2-16:2018 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy... | |
| IEC 60601-2-16:2025 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of HAEMODIALYSIS, HAEMODIAFILTRATION and HAEMOFILTRATION EQUIPMENT, hereafter referred to as HAEMODIALYSIS EQUIPMENT. It applies to HAEMODIALYSIS EQUIPMENT intended for use... | |
| IEC 60601-2-16:2025 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy... | |
| IEC 60601-2-17:2013 applies to the basic safety and essential performance of automatically-contro lled Brachytherapy Afterloading Medical Equipment. This standard does not specify requirements for sealed radioactive sources. This third edition... | |
| IEC 60601-2-18:2009 establishes particular basic safety and essential performance requirements for endoscopic equipment. The minimum safety requirements specified in this particular standard are considered to provide for a practical degree... | |
| IEC 60601-2-19:2009 specifies safety requirements for infant incubators. This particular standard amends and supplements IEC 60601-1:2005, Medical electrical equipment - Part 1: General requirements for basic safety and essential performance. | |
| IEC 60601-2-19:2009+A1:2 016 specifies safety requirements for infantincubators. This particular standard amends and supplements IEC 60601-1:2005, Medical electrical equipment - Part 1: General requirements for basic safety and essential performance. | |
| IEC 60601-2-19:2020 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of INFANT INCUBATORS, as defined in 201.3.209, also referred to as ME EQUIPMENT. If a clause or subclause is specifically... | |
| IEC 60601-2-19:2020 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy... | |
| IEC 60601-2-19:2020+AMD1 :2023 CSV applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of INFANT INCUBATORS, as defined in 201.3.209, also referred to as ME EQUIPMENT. If a clause or subclause... | |
| IEC 60601-2-1:2009 applies to the basic safety and essential performance of electron accelerators in the range 1 MeV to 50 MeV, used for treatment of patients. This particular standard establishes... | |
| IEC 60601-2-1:2009+A1:20 14 applies to the basic safety and essentialperformance of electron accelerators in the range 1 MeV to 50 MeV, used for treatment of patients. This particular standard establishes... | |
| IEC 60601-2-1:2020 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of ELECTRON ACCELERATORS, hereafter referred to as ME EQUIPMENT, in the range 1 MeV to 50 MeV, used for TREATMENT... | |
| IEC 60601-2-20:2009 specifies safety requirements for infant transport incubators. This particular standard amends and supplements IEC 60601-1:2005, Medical electrical equipment - Part 1: General requirements for basic safety and essential... | |
| IEC 60601-2-20:2009+A1:2 016 specifies safety requirements for infanttransport incubators. This particular standard amends and supplements IEC 60601-1:2005, Medical electrical equipment - Part 1: General requirements for basic safety and essential... | |
| IEC 60601-2-20:2020 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of INFANT TRANSPORT INCUBATOR equipment, as defined in 201.3.208, also referred to as ME EQUIPMENT. If a clause or subclause... | |
| IEC 60601-2-20:2020 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy... | |
| IEC 60601-2-20:2020+AMD1 :2023 CSV applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of INFANT TRANSPORT INCUBATOR equipment, as defined in 201.3.208, also referred to as ME EQUIPMENT. If a clause... | |
| IEC 60601-2-21:2009 specifies the safety requirements for infant radiant warmers. This particular standard amends and supplements IEC 60601-1:2005, Medical electrical equipment - Part 1: General requirements for basic safety and... | |
| IEC 60601-2-21:2009+A1:2 016 specifies the safety requirements for infant radiant warmers. This particular standard amends and supplements IEC 60601-1:2005, Medical electrical equipment - Part 1: General requirements for basic safety... | |
| IEC 60601-2-21:2020 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of INFANT RADIANT WARMERS as defined in 201.3.204, also referred to as ME EQUIPMENT. If a clause or subclause is... | |
| IEC 60601-2-21:2020 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy... | |
| IEC 60601-2-21:2020+AMD1 :2023 CSV applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of INFANT RADIANT WARMERS as defined in 201.3.204, also referred to as ME EQUIPMENT. If a clause or... | |
| IEC 60601-2-22:2007+A1:2 012 applies to the safety and essential performance of laser equipment for either surgical, therapeutic, medical diagnostic, cosmetic, or veterinary applications, intended for its use on humans or... | |
| IEC 60601-2-22:2019 applies to the Basic Safety and Essential Performance of laser equipment for surgical, therapeutic, medical diagnostic, cosmetic or veterinary applications, intended for use on humans or animals, classified... | |
| IEC 60601-2-22:2019 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy... | |
| IEC 60601-2-23:2011 applies to the basic safety and essential performance of transcutaneous partial pressure monitoring equipment. It applies to transcutaneous monitors used with adults, children and neonates, and it includes... | |
| IEC 60601-2-24:2012 applies to the basic safety and essential performance of infusion pumps and volumetric infusion controllers. This standard applies to administration sets insofar as their characteristics influence the basic... | |
| IEC 60601-2-25:2011 applies to the basic safety and essential performance of electrocardiographs intended by themselves or as a part of a medical electrical system, for the production of electrocardiogram reports... | |
| IEC 60601-2-26:2012 standard applies to basic safety and essential performance of electroencephalograp hs used in a clinical environment (e.g., hospital, physician's office, etc.). This standard does not cover requirements for... | |
| IEC 60601-2-27:2011 applies to electrocardiographic monitoring equipments used in a hospital environment as well as when used outside the hospital environment, such as in ambulances and air transport. This particular... | |
| IEC 60601-2-28:2010 establishes particular basic safety and essential performance requirements for X-ray tube assemblies for medical diagnosis. This second edition cancels and replaces the first edition published in 1993. This... | |
| IEC 60601-2-28:2017 applies to the basic safety and essential performance of X-ray tube assemblies and to components thereof, intended for medical diagnosis and imaging. Where the general standard IEC 60601-1... | |
| IEC 60601-2-28:2017 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy... | |
| IEC 60601-2-29:2008 establishes requirements to be complied with by manufacturers in the design and construction of radiotherapy simulators; it does not attempt to define their optimum performance requirements. Its purpose... | |
| IEC 60601-2-2:2009 specifies particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories. This particular standard amends and supplements IEC 60601-1... | |
| IEC 60601-2-2:2017 applies to the basic safety and essential performance of HF surgical equipment and HF surgical accessories. HF surgical equipment having a rated output power not exceeding 50 W... | |
| IEC 60601-2-2:2017 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy... | |
| IEC 60601-2-2:2017+AMD1: 2023 CSV applies to the basic safety and essential performance of HF surgical equipment and HF surgical accessories. HF surgical equipment having a rated output power not exceeding... | |
| IEC 60601-2-31:2008 applies to the basic safety and essential performance of external pacemakers powered by an internal electrical power source. The minimum safety requirements specified in this particular standard are... | |
| IEC 60601-2-31:2008+A1:2 011 consists of the second edition (2008) and its amendment 1 (2011). The technical content is therefore identical to the base edition and its amendment and has been... | |
| IEC 60601-2-31:2020 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of EXTERNAL PACEMAKERS powered by an INTERNAL ELECTRICAL POWER SOURCE, hereafter referred to as ME EQUIPMENT. This document applies to... | |
| IEC 60601-2-31:2020 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy... | |
| IEC 60601-2-33 establishes requirements for the safety of MR equipment to provide protection for the patient and the MR worker. It establishes requirements to provide information to the operator, staff... | |
| IEC 60601-2-33:2010 establishes particular basic safety and essential performance requirements for magnetic resonance equipment to provide protection for the patient and the magnetic resonance worker. This third edition cancels and... | |
| IEC 60601-2-33:2010+A1:2 013 establishes particular basic safety and essential performance requirements for magnetic resonance equipment to provide protection for the patient and the magnetic resonance worker. This third edition cancels... | |
| IEC 60601-2-33:2010+A1:2 013+A2:2015 establishes particular basic safety and essential performance requirements for magnetic resonance equipment to provide protection for the patient and the magnetic resonance worker. It has also been... | |
| IEC 60601-2-33:2022 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of MAGNETIC RESONANCE (MR) EQUIPMENT and MAGNETIC RESONANCE (MR) SYSTEMS. This document does not cover the application of MR EQUIPMENT... | |
| IEC 60601-2-34:2011 concerns the basic safety and essential performance of invasive blood pressure monitoring equipment. It amends and supplements IEC 60601-1 (third edition, 2005): Medical electrical equipment - Part 1:... | |
| IEC 60601-2-34:2024 applies to BASIC SAFETY and ESSENTIAL PERFORMANCE of INVASIVE BLOOD PRESSURE MONITORING EQUIPMENT as defined in 201.3.63, hereinafter also referred to as ME EQUIPMENT. This document applies to... | |
| IEC 60601-2-35:2020 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of HEATING DEVICES using BLANKETS, PADS or MATTRESSES in medical use, also referred to as ME EQUIPMENT. HEATING DEVICES intended... | |
| IEC 60601-2-35:2020+AMD1 :2023 CSV applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of HEATING DEVICES using BLANKETS, PADS or MATTRESSES in medical use, also referred to as ME EQUIPMENT. HEATING... | |
| IEC 60601-2-36:2014 applies to basic safety and essential performance of equipment for extracorporeally induced lithotripsy including equipment for other medical applications of therapeutic extracorporeally induced focused pressure pulses. The applicability... | |
| IEC 60601-2-37:2007+A1:2 015 Applies to the basic safety and essential performance of ultrasonic diagnostic equipment. The approach and philosophy used in drafting this particular standard for safety of ultrasonic diagnostic... | |
| IEC 60601-2-37:2024 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of ULTRASONIC DIAGNOSTIC EQUIPMENT as defined in 201.3.217, hereinafter referred to as ME EQUIPMENT. If a clause or subclause is... | |
| IEC 60601-2-37:2024 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy... | |
| IEC 60601-2-39:2018 applies to the basic safety and essential performance of peritoneal dialysis medical electrical equipment. It applies to peritoneal dialysis equipment intended for use either by medical staff or... | |
| IEC 60601-2-39:2018 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy... | |
| IEC 60601-2-39:2024 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of PERITONEAL DIALYSIS ME EQUIPMENT, hereafter referred to as PD EQUIPMENT. It applies to PD EQUIPMENT intended for use either... | |
| IEC 60601-2-3:2012 specifies the requirements for the basic safety and essential performance of short-wave therapy equipment. Short-wave therapy equipment are defined as medical equipment for the therapeutic treatment of a... | |
| IEC 60601-2-3:2012+A1:20 16 specifies the requirements for the basic safety and essential performance of short-wave therapy equipment. Short-wave therapy equipment are defined as medical equipment for the therapeutic treatment of... | |
| IEC 60601-2-3:2012+AMD1: 2016+AMD2:2022 CSV specifies the requirements for the basic safety and essential performance of short-wave therapy equipment. Short-wave therapy equipment are defined as medical equipment for the therapeutic treatment... | |
| IEC 60601-2-40:2016 applies to the basic safety and essential performance of electromyographs and evoked response equipment, hereafter referred to as ME equipment. ME equipment intended for transcutaneous electrical nerve stimulators... | |
| IEC 60601-2-40:2024 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of ELECTROMYOGRAPHS and EVOKED RESPONSE EQUIPMENT, hereafter referred to as ME EQUIPMENT. The following ME EQUIPMENT are excluded: - ME... | |
| IEC 60601-2-40:2024 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy... | |
| IEC 60601-2-41:2009 applies to the basic safety and essential performance of surgical luminaires and luminaires for diagnosis. It amends and supplements IEC 60601-1 (third Edition 2005), hereinafter referred to as... | |
| IEC 60601-2-41:2009+A1:2 013 applies to the basic safety and essential performance of surgical luminaires and luminaires for diagnosis. It amends and supplements IEC 60601-1 (third Edition 2005), hereinafter referred to... | |
| IEC 60601-2-41:2021 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of SURGICAL LUMINAIRES and LUMINAIRES FOR DIAGNOSIS, hereafter referred to as ME EQUIPMENT. If a clause or subclause is specifically... | |
| IEC 60601-2-43:2010 establishes particular basic safety and essential performance requirements for the design and manufacture of X ray equipment for radioscopically guided interventional procedures. It specifies information which is to... | |
| IEC 60601-2-43:2010+A1:2 017 establishes particular basic safety and essential performance requirements for the design and manufacture of X ray equipment for radioscopically guided interventional procedures. It specifies information which is... | |
| IEC 60601-2-43:2010+A1:2 017+A2:2019 establishes particular basic safety and essential performance requirements for the design and manufacture of X ray equipment for radioscopically guided interventional procedures. It specifies information which is... | |
| IEC 60601-2-43:2022 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of both FIXED and MOBILE X RAY EQUIPMENT declared by the MANUFACTURER to be suitable for RADIOSCOPICALLY GUIDED INTERVENTIONAL PROCEDURES,... | |
| IEC 60601-2-43:2022 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy... | |
| IEC 60601-2-44:2009 applies to the basic safety and essential performance of CT scanners. The scope of IEC 60601-2-44:2009 is limited to CT scanners intended to be used for both head... | |
| IEC 60601-2-44:2009+A1:2 012 applies to the basic safety and essential performance of CT scanners. The scope of IEC 60601-2-44:2009 is limited to CT scanners intended to be used for both... | |
| IEC 60601-2-44:2009+A1:2 012+A2:2016 applies to the basic safety and essential performance of CT scanners. The scope of IEC 60601-2-44:2009 is limited to CT scanners intended to be used for both... | |
| IEC 60601-2-45:2011 applies to the basic safety and essential performance of mammographic X-ray equipment and mammographic stereotactic devices. IEC 60601-2-45:2011 addresses the system level of mammographic X-ray equipment, which consists... | |
| IEC 60601-2-45:2011+A1:2 015 applies to the basic safety and essential performance of mammographic X-ray equipment and mammographic stereotactic devices. IEC 60601-2-45:2011 addresses the system level of mammographic X-ray equipment, which... | |
| IEC 60601-2-45:2011+AMD1 :2015+AMD2:2022 CSV applies to the basic safety and essential performance of mammographic X-ray equipment and mammographic stereotactic devices. IEC 60601-2-45:2011 addresses the system level of mammographic X-ray equipment,... | |
| IEC 60601-2-46:2010 specifies safety requirements for operating tables, whether or not having electrical parts, including transporters, used for the transportation of the table top to or from the base or... | |
| IEC 60601-2-46:2016 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy... | |
| IEC 60601-2-46:2016 specifies safety requirements for operating tables, whether or not having electrical parts, including transporters, used for the transportation of the operating table top to or from the base... | |
| IEC 60601-2-46:2023 CMV contains both the official standard and its commented version. The commented version provides you with a quick and easy way to compare all the changes between IEC... | |
| IEC 60601-2-46:2023 specifies safety requirements for operating tables, whether or not having electrical parts, including transporters, used for the transportation of the operating table top to or from the base... | |
| IEC 60601-2-47:2012 concerns the basic safety and essential performance of AMBULATORY ELECTROCARDIOGRAPHIC SYSTEMS. It amends and supplements the general standard IEC 60601-1 (third edition 2005). The requirements of this particular... | |
| IEC 60601-2-49:2011 applies to the basic safety and essential performance requirements of multifunction patient monitoring equipment. It applies to medical electrical equipment used in a hospital environment as well as... | |
| IEC 60601-2-4:2010 establishes particular basic safety and essential performance requirements for cardiac defibrillators. This third edition cancels and replaces the second edition published in 2002. This edition constitutes a technical... | |
| IEC 60601-2-4:2010+A1:20 18 establishes particular basic safety and essential performance requirements for cardiac defibrillators. This third edition cancels and replaces the second edition published in 2002. This edition constitutes a... | |
| IEC 60601-2-50:2009 establishes particular basic safety and essential performance requirements for infant phototherapy equipment, which reduce the safety hazards to patients and operators as much as possible, and specifies tests... | |
| IEC 60601-2-50:2009+A1:2 016 establishes particular basic safety and essential performance requirements for infant phototherapy equipment, which reduce the safety hazards to patients and operators as much as possible, and specifies... | |
| IEC 60601-2-50:2020 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of INFANT PHOTOTHERAPY EQUIPMENT, as defined in 201.3.203, also referred to as ME EQUIPMENT. If a clause or subclause is... | |
| IEC 60601-2-50:2020 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy... | |
| IEC 60601-2-50:2020+AMD1 :2023 CSV applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of INFANT PHOTOTHERAPY EQUIPMENT, as defined in 201.3.203, also referred to as ME EQUIPMENT. If a clause or... | |
| IEC 60601-2-52:2009 applies to the basic safety and essential performance of medical beds intended for adults. This first edition cancels and replaces the first edition of IEC 60601-2-38, published in... | |
| IEC 60601-2-52:2009+A1:2 015 applies to the basic safety and essential performance of medical beds intended for adults. IEC 60601-2-52:2009 is the realization of much work in alignment, and scope adjustment... | |
| IEC 60601-2-54:2009 applies to the basic safety and essential performance of medical electrical equipment and medical electrical systems intended to be used for projection radiography and radioscopy. The minimum safety... | |
| IEC 60601-2-54:2009+A1:2 015 applies to the basic safety and essential performance of medical electrical equipment and medical electrical systems intended to be used for projection radiography and radioscopy. The minimum... | |
| IEC 60601-2-54:2009+A1:2 015+A2:2018 applies to the basic safety and essential performance of medical electrical equipment and medical electrical systems intended to be used for projection radiography and radioscopy. The minimum... | |
| IEC 60601-2-54:2022 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of ME EQUIPMENT and ME SYSTEMS intended to be used for projection RADIOGRAPHY and INDIRECT RADIOSCOPY. IEC 60601-2-43 applies to... | |
| IEC 60601-2-54:2022 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy... | |
| IEC 60601-2-57:2011 applies to basic safety and essential performance of equipment incorporating one or more sources of optical radiation in the wavelength range 200 nm to 3 000 nm, with... | |
| IEC 60601-2-57:2023 applies to basic safety and essential performance of equipment incorporating one or more sources of optical radiation in the wavelength range 200 nm to 3 000 nm, with... | |
| IEC 60601-2-62:2013 applies to the basic safety and essential performance of HIGH INTENSITY THERAPEUTIC ULTRASOUND EQUIPMENT. This International Standard adds or replaces clauses listed in the IEC 60601-1 that are... | |
| IEC 60601-2-63:2012 applies to the basic safety and essential performance of dental extra-oral X-ray equipment, hereafter also called ME equipment. The scope includes ME systems containing such ME equipment. This... | |
| IEC 60601-2-63:2012+A1:2 017 applies to the basic safety and essential performance of dental extra-oral X-ray equipment, hereafter also called ME equipment. The scope includes ME systems containing such ME equipment. | |
| IEC 60601-2-63:2012+A1:2 017+A2:2021 applies to the basic safety and essential performance of dental extra-oral X-ray equipment, hereafter also called ME equipment. The scope includes ME systems containing such ME equipment. | |
| IEC 60601-2-64:2014 applies to the basic safety and essential performance of Light Ion Beam Medical Electrical equipment, hereafter referred to as ME equipment, used for treatment of patients. This particular... | |
| IEC 60601-2-65:2012 applies to the basic safety and essential performance of dental intra-oral X-ray equipment and its main components. The scope of this standard is restricted to X-ray equipment where... | |
| IEC 60601-2-65:2012+A1:2 017 applies to the basic safety and essential performance of dental intra-oral X-ray equipment and its main components. The scope of this standard is restricted to X-ray equipment... | |
| IEC 60601-2-65:2012+A1:2 017+A2:2021 applies to the basic safety and essential performance of dental intra-oral X-ray equipment and its main components. The scope of this standard is restricted to X-ray equipment... | |
| IEC 60601-2-66:2012 International Standard applies to the basic safety of hearing instruments and hearing instrument systems. Hazards inherent in the intended physiological function of hearing instruments or hearing instrument systems... | |
| IEC 60601-2-66:2015 applies to the basic safety of hearing instruments and hearing instrument systems, hereafter also referred to as ME equipment or ME system. This second edition cancels and replaces... | |
| IEC 60601-2-66:2019 applies to the BASIC SAFETY of HEARING AIDS and HEARING AID SYSTEMS, hereafter also referred to as ME EQUIPMENT or ME SYSTEM. IEC 60601-2-66:2019 cancels and replaces the... | |
| IEC 60601-2-66:2019 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy... | |
| IEC 60601-2-68:2014 applies to the basic safety and essential performance of X-ray based image-guided radiotherapy (IGRT) equipment for use with External Beam Equipment (EBE). This particular standard covers safety aspects... | |
| IEC 60601-2-6:2012 specifies the minimum requirements considered to provide for a practical degree of safety in the operation of microwave therapy equipment. This particular standard amends and supplements IEC 60601-1... | |
| IEC 60601-2-6:2012+A1:20 16 specifies the minimum requirements considered to provide for a practical degree of safety in the operation of microwave therapy equipment. This particular standard amends and supplements IEC... | |
| IEC 60601-2-6:2012+AMD1: 2016+AMD2:2022 CSV specifies the minimum requirements considered to provide for a practical degree of safety in the operation of microwave therapy equipment. This particular standard amends and supplements... | |
| IEC 60601-2-75:2017 applies to the basic safety and essential performance of photodynamic therapy and photodynamic diagnosis equipment. Hazards inherent in the intended physiological function of ME equipment or ME systems... | |
| IEC 60601-2-75:2017+AMD1 :2023 CSV applies to the basic safety and essential performance of photodynamic therapy and photodynamic diagnosis equipment. Hazards inherent in the intended physiological function of ME equipment or... | |
| IEC 60601-2-76:2018 applies to the basic safety and essential performance of low energy ionized gas haemostasis equipment. Hazards inherent in the intended physiological function of ME Equipment or ME Systems... | |
| IEC 60601-2-76:2018+AMD1 :2023 CSV applies to the basic safety and essential performance of low energy ionized gas haemostasis equipment. Hazards inherent in the intended physiological function of ME Equipment or... | |
| IEC 60601-2-83:2019 is applicable to the BASIC SAFETY and ESSENTIAL PERFORMANCE of HOME LIGHT THERAPY EQUIPMENT, intended for use in the HOME HEALTHCARE ENVIRONMENT. HOME LIGHT THERAPY EQUIPMENT is typically... | |
| IEC 60601-2-83:2019+AMD1 :2022 CSV is applicable to the basic safety and essential performance of home light therapy equipment, intended for use in the home healthcare environment. Home light therapy equipment... | |
| IEC 60601-2-8:2010 establishes particular basic safety and essential performance requirements for therapeutic X-ray equipment with nominal X-ray tube voltages in the range 10 kV to 1 MV when connected to... | |
| IEC 60601-2-8:2010+A1:20 15 establishes particular basic safety and essential performance requirements for therapeutic X-ray equipment with nominal X-ray tube voltages in the range 10 kV to 1 MV when connected... | |
| IEC 60603-2:1995 applies to groups of related connectors for use with printed boards. They range from connectors with high contact density for low-voltage applications (Styles B and C) to connectors... | |
| IEC 60603-7-1:2009 covers 8-way shielded free and fixed connectors. Specifies the dimensions, mechanical, electrical and environmental characteristics and tests, in relation to the shield, additional to those in IEC 60603-7. | |
| IEC 60603-7-1:2011 covers 8-way shielded free and fixed connectors. It specifies the dimensions, mechanical, electrical and environmental characteristics and tests, in relation to the shield, additional to those in IEC... | |
| IEC 60603-7-2:2010 covers 8-way, unshielded, free and fixed connectors, references dimensional, mechanical, electrical and environmental characteristics and tests in IEC 60603-7, and specifies electrical transmission requirements for frequencies up to... | |
| IEC 60603-7-3:2010 covers 8-way, shielded, free and fixed connectors, references dimensional, mechanical, electrical and environmental characteristics and tests in IEC 60603-7 and IEC 60603-7-1, and specifies electrical transmission requirements for... | |
| IEC 60603-7-41:2010 covers 8-way, unshielded, free and fixed connectors, references dimensional, mechanical, electrical and environmental characteristics and tests in IEC 60603-7, and specifies electrical transmission requirements, including power sum alien... | |
| IEC 60603-7-4:2010 covers 8-way, unshielded, free and fixed connectors, references dimensional, mechanical, electrical and environmental characteristics and tests in IEC 60603-7, and specifies electrical transmission requirements for frequencies up to... | |
| IEC 60603-7-51:2010 covers 8-way, shielded, free and fixed connectors, references dimensional, mechanical, electrical and environmental characteristics and tests in IEC 60603-7, and specifies electrical transmission requirements, including power sum alien... | |
| IEC 60603-7-5:2010 covers 8-way, shielded, free and fixed connectors and references dimensional, mechanical, electrical and environmental characteristics and tests in IEC 60603-7 and IEC 60603-7-1, and specifies electrical transmission requirements... | |
| IEC 60603-7-71:2010 covers 8-way, shielded, free and fixed connectors, references dimensional, mechanical, electrical and environmental characteristics and tests in IEC 60603-7, and specifies electrical transmission requirements, including power sum alien... | |
| IEC 60603-7-7:2010 covers 8-way, shielded, free and fixed connectors, references dimensional, mechanical, electrical and environmental characteristics and tests in IEC 60603-7 and IEC 60603-7-1, and specifies electrical transmission requirements for... | |
| IEC 60603-7-81:2015 Covers 8-way, shielded, free and fixed connectors, references dimensional, mechanical, electrical and environmental characteristics and tests in IEC 60603-7, and specifies electrical transmission requirements, including power sum alien... | |
| IEC 60603-7-82:2016 covers 8-way, 12 contacts, shielded, free and fixed connectors, references dimensional, mechanical, electrical and environmental characteristics and tests in IEC 60603-7-7, and specifies electrical transmission requirements, including power... | |
| IEC 60603-7:2008 covers 8-way unshielded free and fixed connectors and is intended to specify the common dimensions, mechanical, electrical and environmental characteristics and tests for the family of IEC 60603-7-x... | |
| IEC 60603-7:2008+A1:2011 covers 8-way unshielded free and fixed connectors and is intended to specify the common dimensions, mechanical, electrical and environmental characteristics and tests for the family of IEC 60603-7-x... | |
| IEC 60603-7:2008+A1:2011 +A2:2019 covers 8-way unshielded free and fixed connectors and is intended to specify the common dimensions, mechanical, electrical and environmental characteristics and tests for the family of IEC... | |
| IEC 60603-7:2020 covers 8-way, unshielded, free and fixed connectors and is intended to specify the common dimensions (interface dimensions), mechanical, electrical and environmental characteristics and tests for the family of... | |
| IEC 60603-7:2020 RLV contains both the official IEC International Standard and its Redline version. The Redline version is available in English only and provides you with a quick and easy... | |
| IEC 60609-1:2004 provides a basis for the formulation of guarantees applied to cavitation pitting for reaction hydraulic turbines, storage pumps and pump-turbines. It addresses the measurement and evaluation of the... | |
| IEC 60609-2:1997 serves as a basis for the formulation of guarantees on cavitation pitting on Pelton turbine runners. It also provides a basis for the measurement and evaluation of the... | |
| IEC 60613:2010 applies to X-ray tube assemblies either with a rotating anode X-ray tube or a stationary anode X-ray tube, intended for use in medical diagnosis. For an X-ray tube... | |
| IEC TR 62348:2012 provides a tool to assist users of IEC 60601-1:2005 to assess the impact of the most significant changes in Amendment 1:2012, and to trace requirements between the... | |
| Incorporates Amendment No. 1 (1987). | |
| Incorporates the revisions to, and facilitates the application of, the Collateral Standards IEC 601-1-2 and IEC 601-1-3, and the consequent revisions relevant to their use with IEC 601-2-29. | |
| It applies to the design of operating and environmental test cycles referred to in 8.1 and 8.2 of IEC 605-1. | |
| It includes primarily a revision of the requirements of the separation devices regarding creepage distances and air clearances. Requirements for muliple portable socket-outlets when used in systems are included. | |
| It is applicable to printed board connectors designed for use in equipment for telecommunication and electronic data processing and in electronic equipment or devices employing similar techniques. The object is... | |
| It is intended to facilitate interpretation and application of the General Standard. Identifies additional aspects of safety which were not previously covered. References to the Collateral Standards IEC 601-1-1, 601-1-2,... | |
| Medical practice is increasingly using medical electrical equipment for observation and treatment of patients. use errors caused by inadequate medical electrical equipment usability have become an increasing cause for concern. | |
| Provides a guide to the methods which should be followed by users for the handling and mounting of variable capacitors. Gives specific information on package and storage, mounting and assembly,... | |
| Provides statistical methods for evaluating point estimates, confidence intervals, prediction intervals and tolerance intervals for the failure rate of items whose time to failure follows an exponential distribution. | |
| Serves as a basis for the formulation of guarantees applying to cavitation pitting, and also for the measurement and evaluation of the amount of cavitation pitting on certain specified parts... | |
| Specifies basic safety and essential performance requirements and tests for alarm systems in medical electrical equipment and medical electrical systems and to provide guidance for their application. This is accomplished... | |
| Specifies essential requirements for the performance of transcutaneous oxygen and carbon dioxide partial pressure monitoring equipment. Applies to transcutaneous monitors intended for use with adults, children and neonates, and includes... | |
| Specifies mechanical and environmental requirements, and electrical transmission requirements for frequencies up to 250 MHz. These connectors are typically used as category 6 connectors in class E cabling systems specified... | |
| Specifies particular requirements for the safety of anaesthetic workstations for inhalational anaesthesia intended for human use supplied complete, as well as particular requirements for individual devices which are intended to... | |
| Specifies particular requirements for the safety of automatic cycling indirect blood pressure monitoring equipment, with special attention being paid to the avoidance of hazards due to the inflation process. | |
| Specifies particular requirements for the safety of dosimeters used in medical practice in the patient environment for radiotherapy. (Non-medical dosimeters are dealt with in IEC 348.) | |
| Specifies particular requirements for the safety of dosimeters used in medical practice in the patient environment for radiotherapy. (Non-medical dosimeters are dealt with in IEC 60348.) | |
| Specifies particular requirements for the safety of electrical stimulators of muscles and nerves in the specialized practice of physical medicine. It excludes stimulators used with implanted electrodes, brain stimulation, neurological... | |
| Specifies particular requirements for the safety of high voltage generators of diagnostic X-ray generators operating between 10 kV and 400 kV. | |
| Specifies particular requirements for the safety of high-frequency medical electrical equipment and its associated accessories used in surgical cutting or coagulation. | |
| Specifies particular requirements for the safety of therapeutic X-ray generators operating with nominal X-ray tube voltages from 10 kV to 400 kV inclusive. | |
| Specifies particular requirements for the safety, including essential performance, of automatic cycling non-invasive blood pressure monitoring equipment, with special attention being paid to the avoidance of hazards due to the... | |
| Specifies particular safety and essential performance requirements for individual devices designed for use in an anaesthetic system as well as specific requirements for the anaesthetic gas delivery system. This standard... | |
| Specifies procedures to verify the assumption of a constant failure rate or constant failure intensity as defined in IEC 60050(191). These procedures are applicable whenever it is necessary to verify... | |
| Specifies requirements and tests for electromagnetic compatibility of equipment and systems and serves as the basis of electromagnetic compatibility requirements and tests in Particular Standards (60601-2-series). The existence of electromagnetic... | |
| Specifies requirements and tests for electromagnetic compatibility of medical electrical equipment and medical electrical systems and serves as the basis of electromagnetic compatibility requirements and tests in Particular Standards. | |
| Specifies requirements applicable to infant phototherapy equipment which by means of visible radiation serve to reduce bilirubin in the body of infants suffering from icterus in the first months of... | |
| Specifies requirements for a process to analyse, design, verify and validate the usability, as it relates to basic safety and essential performance of medical electrical equipment. This collateral standard addresses... | |
| Specifies requirements for alarm systems and alarm signals in medical electrical equipment and medical electrical systems. It also provides guidance for the application of alarm systems. The object of this... | |
| Specifies requirements for conduits of circular cross-section for the protection of the conductors and/or cables in electrical installations. | |
| Specifies requirements for handlamps and similar portable luminaires which are held in the hand when used, for use with tungsten filament and tubular fluorescent lamps on supply voltages not exceeding... | |
| Specifies requirements for photo and film luminaires (non-professional) for use with low-pressure tungsten halogen lamps, specified in IEC 357. | |
| Specifies requirements for photo and film luminaires (non-professional) for use with low-pressure tungsten halogen lamps, specified in IEC 60357. | |
| Specifies requirements for pliable self-recovering plain and corrugated conduits of insulating materials. | |
| Specifies requirements for safety of electrically operated hospital beds. The object of this standard is to keep the safety hazards to patients, operators and the environment as low as possible,... | |
| Specifies requirements for the development (analysis, design, verification and validation) of a physiologic closed-loop controller (PCLC) as part of a physiologic closed-loop control system (PCLCS) in medical electrical equipment and... | |
| Specifies requirements for the process by which a programmable electrical medical system is designed. Serves as the basis of requirements of Particular Standards, including serving as a guide to safety... | |
| Specifies requirements for the safety of cardiac defibrillators and cardiac defibrillator-monito rs incorporating a capacitive energy storage device. | |
| Specifies requirements for the safety of cardiac defibrillators. The requirements are followed by specifications for the relevant tests. | |
| Specifies requirements for the safety of high frequency surgical equipment used in medical practice. This third edition of IEC 60601-2-2 cancels and replaces the second edition published in 1991, and... | |
| Specifies requirements for the safety of microwave therapy equipment used in medical practice, but does not apply to equipment specified for hyperthermia. | |
| Specifies requirements for the safety of multifunction patient monitoring equipment. The scope of this standard is restricted to equipment having either more than one applied part or more than one... | |
| Specifies requirements for the safety, design and construction of gamma beam equipments when used for radiotherapy in human medical practice. Applies to equipment which is intended to deliver a gamma... | |
| Specifies requirements for the safety, including essential performance, of transcutaneous partial pressure monitoring equipment, whether this equipment is stand alone or part of a system. Applies to transcutaneous monitors used... | |
| Specifies requirements for threadable and non-threadable plain rigid metal conduits. | |
| Specifies safety requirements for operating tables, whether or not having electrical parts, including transporters used for the transportation of the table top to or from the base or pedestal of... | |
| Specifies the minimum safety requirements for peritoneal dialysis equipment. Applies to equipment intended for use either by medical staff or under supervision of medical experts, including equipment operated by the... | |
| Specifies the minimum safety requirements for single patient haemodialysis, haemodiafiltration and haemofiltration equipment. These devices are intended for use either by medical staff or under the supervision of medical expertise,... | |
| Specifies the particular requirements for the electrical and mechanical safety of medical electron accelerators. It contains new sub-clauses which are additions to section one of IEC 601-2-1, and a new... | |
| Specifies the particular requirements for the safety of transcutaneous partial pressure monitoring equipment. Applies to transcutaneous monitors used with adults, children and neonates and includes the use of these devices... | |
| Specifies the particular safety requirements for ambulatory electrocardiographic systems. Within the scope of this standard are systems of the following types: a) systems that provide continuous recording and continuous analysis... | |
| Specifies the particular safety requirements for electrocardiographic monitoring equipment defined as 'equipment and associated electrodes for the monitoring and/or recording of heart action potentials and displaying the resultant data locally... | |
| Specifies the particular safety requirements for electrocardiographs, intended for the production of detachable electrocardiograms for diagnostic purposes. Also applies to vectorcardiographs and equipment for stress testing. | |
| Specifies the particular safety requirements for electroencephalograp hs defined as medical electrical equipment intended for the production of graphic recordings and/or a visual display of electrical activity of the brain... | |
| Specifies the particular safety requirements for electroencephalograp hs, i.e. devices to produce an electroencephalogram . This Particular Standard amends and supplements IEC 60601-1 (1988): Medical electrical equipment - Part 1:... | |
| Specifies the particular safety requirements for external pacemakers powered by an internal electrical power source. Applies also to patient cables but does not apply to equipment which can be directly... | |
| Specifies the particular safety requirements, including essential performance, for electrocardiographic (ECG) monitoring equipment. This standard is applicable to equipment used in a hospital environment. If the equipment is used outside... | |
| Specifies the requirements for infusion pumps, infusion controllers, syringe pumps and pumps for ambulatory use. These devices are intended for use by medical staff and home patients as prescribed and... | |
| Specifies the requirements for safety of ultrasonic equipment used in medical practice. | |
| Specifies the safety requirements for ventilators, as defined below, intended for use in critical care settings. Ventilator: automatic equipment that is intended to augment or provide ventilation of the lungs... | |
| Specifies the safety requirements for X-ray tube assemblies for medical diagnoses and components thereof, specified for use in medical X-ray equipment including equipment for computed tomography, that incorporates a specified... | |
| Standard | |
| Supplementing the general safety requirements of medical equipment formulated in the basic publication IEC 601-1, this standard gives specific requirements for lung ventilators that incorporate electrical devices designed for medical... | |
| The contents of the corrigendum of April 2006 have been included in this copy. | |
| The contents of the corrigendum of December 1989 have been included in this copy. | |
| The contents of the corrigendum of January 2002 have been included in this copy. | |
| The mainstay of safety standards in all the rapidly evolving technology of electromedical equipment, the second (1988) edition of IEC 601-1 called for updating through this first Amendment. | |
| The object of this standard is 1. to formulate appropriate design and manufacturing requirements for the safety of mammographic X-ray equipment and mammographic stereotactic devices, reflecting the particular characteristics and... | |
| The original publication established requirements for safety levels of radiation for medical electron accelerators in medical practice. This second amendment specifies test procedures for those items where a radiation safety... | |
| The use of afterloading equipment for brachytherapy purposes may expose patients to danger if the equipment fails to deliver the required dose to the patient, or if the equipment design... | |
| This collateral standard applies to electromagnetic compatibility of medical electrical equipment and medical electrical systems. The object of this collateral standard is to specify general requirements and tests for electromagnetic... | |
| This collateral standard applies to X-ray equipment and to subassemblies of such equipment, where radiological images of a human patient are used for diagnosis, planning or guidance of medical procedures. | |
| This is the major revised and updated baseline of standards for the safety of all medical electrical equipment used by or under the supervision of qualified personnel in the general... | |
| This Part 2 of IEC 60601 specifies requirements for infant radiant warmers. Requirements for equipment intended for use outside a hospital baby care environment, equipment having a heated mattress, and... | |
| This Part 2-8 of IEC 60598 specifies requirements for handlamps and similar portable luminaires which are held in the hand, hooked up or resting on a surface for use with... | |
| This Particular Standard specifies requirements and tests for the safety of ultrasonic physiotherapy equipment. It amends and supplements IEC 60601-1 (second edition, 1988) including Amendments 1 and 2, hereinafter referred... | |
| This Particular Standard specifies requirements for the safety of high frequency surgical equipment and hf surgical accessories used in medical practice. hf surgical equipment having a rated output power not... | |
| This publication also bears the number QC 010000, which is the specification number in the IEC Quality Assessment System for Electronic Components (IECQ). It is applicable to printed board connectors... | |
| This publication also bears the number QC 010000XX0004 which is the specification number in the IEC Quality Assessment System for Electronic Components (IECQ). | |
| This publication establishes particular requirements for the safety of remote-controlled automatically-driven electromedical equipment for gamma-ray therapy of human subjects using afterloading. Its specifications include requirements for equipment which contain and... | |
| This second, updated edition deals with electrical, thermal and loading characteristics of rotating anode X-ray tubes and X-ray tube assemblies intended for use in medical diagnosis, concerning their behaviour during... | |
| This section is applicable to portable equipment for non-stationary use covered by IEC 60721-3-7. The degree of simulation is low. Contains preferred test conditions as given in IEC 60605-1. During... | |
| This standard concerns the safety of short-wave therapy equipment having a rated outpout power not exceeding 500 W. This second edition revises earlier shortcomings and deals in greater detail with... | |
| This standard establishes safety requirements for baby incubators with the view to minimizing hazards to the patient and user. It also specifies tests by which compliance requirements can be verified. | |
| This standard establishes safety standards for the safety of transport incubators which minimize hazards to the patient and user. lt also specifies tests to verify compliance with the requirements. It... | |
| This standard is the first of a new series of collateral standards that specify general requirements for safety applicable to a group of electromedical equipment not fully addressed in the... | |
| This standard specifies requirements for the safety of endoscopic equipment and integrated instrumentation used for medical diagnosis and therapy. It is subdivided into five applications concerning endoscopes for (a) direct... | |
| This standard specifies requirements for the safety of gamma beam therapy equipment intended for radiotherapy in human medical practice and includes equipment in which the selection and display of operating... |
| << Prev | Next >> |