IEC Medical Collection
This collection contains documents from the following standards organization(s): International Electrotechnical Commission 1 2 3 > >
| IEC 60336 | EN-Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Characteristics of focal spots-Fourth Edition | |
| IEC 60336 CORR 1 | EN-Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Characteristics of focal spots CORRIGENDUM 1-Fourth Edition | |
| IEC 60364-7-710 | EN-Electrical installations of buildings Part 7-710: Requirements for special installations or locations Medical locations-First Edition | |
| IEC 60522 | EN-Determination of the Permanent Filtration of X-Ray Tube Assemblies-Second Edition | |
| IEC 60526 | EN-High-Voltage Cable Plug and Socket Connections for Medical X-Ray Equipment-Second Edition | |
| IEC 60580 | EN-Medical Electrical Equipment - Dose Area Product Meters-Second Edition | |
| IEC 60601-1 | EN-Medical electrical equipment - Part 1: General requirements for basic safety and essential performance-Third Edition | |
| IEC 60601-1 CORR 1 | EN-Medical electrical equipment - Part 1: General requirements for basic safety and essential performance CORRIGENDUM 1-Third Edition | |
| IEC 60601-1 CORR 2 | EN-Medical electrical equipment - Part 1: General requirements for basic safety and essential performance-Edition 3.0 | |
| IEC 60601-1 INT 1 | EN-MEDICAL ELECTRICAL EQUIPMENT - Part 1: General requirements for basic safety and essential performance-Edition 3.0 | |
| IEC 60601-1 INT 2 | EN-MEDICAL ELECTRICAL EQUIPMENT - Part 1: General requirements for basic safety and essential performance-Edition 3.0 | |
| IEC 60601-1 SET | ||
| IEC 60601-1-1 | EN-Medical Electrical Equipment - Part 1-1: General Requirements for Safety - Collateral Standard: Safety Requirements for Medical Electrical Systems-Edition 2.0 | |
| IEC 60601-1-10 | EN-Medical electrical equipment - Part 1-10: General requirements for basic safety and essential performance - Collateral Standard: Requirements for the development of physiologic closed-loop controllers-Edition 1.0 | |
| IEC 60601-1-11 | EN-Medical electrical equipment - Part 1-11: General requirements for basic safety and essential performance - Collateral Standard: Requirements for medical electrical equipment and medical electrical systems used i | |
| IEC 60601-1-2 | EN-Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral standard: Electromagnetic compatibility - Requirements and tests-Edition 3.0 | |
| IEC 60601-1-2 INT 1 | EN-Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral standard: Electromagnetic compatibility - Requirements and tests-Edition 3.0 | |
| IEC 60601-1-3 | EN-Medical Electrical Equipment - Part 1: General Requirements for Safety 3. Collateral Standard: General Requirements for Radiation Protection in Diagnostic X-Ray Equipment-Edition 2.0 | |
| IEC 60601-1-4 | EN-Medical Electrical Equipment - Part 1-4: General Requirements for Safety - Collateral Standard: Programmable Electrical Medical Systems-Edition 1.1; Edition 1:1996 Consolidated with Amendment 1:1999 | |
| IEC 60601-1-6 | EN-Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability-Edition 3.0 | |
| IEC 60601-1-8 | EN-Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral Standard: General requirements tests and guidance for alarm systems in medical electrical equ | |
| IEC 60601-1-9 | EN-Medical electrical equipment - Part 1-9: General requirements for basic safety and essential performance - Collateral Standard: Requirements for environmentally conscious design-Edition 1.0 | |
| IEC 60601-2-1 | EN-Medical electrical equipment - Part 2-1: Particular requirements for the basic safety and essential performance of electron accelerators in the range 1 MeV to 50 MeV-Edition 3.0 | |
| IEC 60601-2-10 | EN-Medical Electrical Equipment Part 2: Particular Requirements for the Safety of Nerve and Muscle Stimulators First Edition | |
| IEC 60601-2-10 AMD 1 | EN-Medical Electrical Equipment Part 2: Particular Requirements for the Safety of Nerve and Muscle Stimulators First Edition | |
| IEC 60601-2-10 AMD 1 | EN-Amendment 1 Medical electrical equipment - Part 2-10: Particular requirements for the safety of nerve and muscle stimulators | |
| IEC 60601-2-10 CORR 1 | EN-Medical Electrical Equipment Part 2: Particular Requirements for the Safety of Nerve and Muscle Stimulators | |
| IEC 60601-2-11 | EN-Medical Electrical Equipment - Part 2: Particular Requirements for the Safety of Gamma Beam Therapy Equipment-Edition 2; Amendment 1: 07/2004 (English Only Amendment) | |
| IEC 60601-2-12 | EN-Medical Electrical Equipment - Part 2: Particular Requirements for the Safety of Lung Ventilators - Critical Care Ventilators-Second Edition; Supersedes ISO 10651-1: 1993 | |
| IEC 60601-2-13 | EN-Medical electrical equipment - Part 2-13: Particular requirements for the safety and essential performance of anaesthetic systems-Edition 3.1; Consolidated Reprint | |
| IEC 60601-2-16 | EN-Medical electrical equipment - Part 2-16: Particular requirements for basic safety and essential performance of haemodialysis haemodiafiltration and haemofiltration equipment-Edition 3.0 | |
| IEC 60601-2-16 CORR 1 | EN-Medical electrical equipment - Part 2-16: Particular requirements for basic safety and essential performance of haemodialysis haemodiafiltration and haemofiltration equipment CORRIGENDUM 1-Edition 3.0 | |
| IEC 60601-2-17 | EN-Medical electrical equipment Part 2-17: Particular requirements for the safety of automatically-controlled brachytherapy afterloading equipment-Edition 2 | |
| IEC 60601-2-18 | EN-Medical electrical equipment - Part 2-18: Particular requirements for the basic safety and essential performance of endoscopic equipment-Edition 3.0 | |
| IEC 60601-2-19 | EN-Medical electrical equipment - Part 2-19: Particular requirements for the basic safety and essential performance of infant incubators-Edition 2.0 | |
| IEC 60601-2-2 | EN-Medical electrical equipment - Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories-Edition 5.0 | |
| IEC 60601-2-20 | EN-Medical electrical equipment - Part 2-20: Particular requirements for the basic safety and essential performance of infant transport incubators-Edition 2.0 | |
| IEC 60601-2-21 | EN-Medical electrical equipment - Part 2-21: Particular requirements for the basic safety and essential performance of infant radiant warmers-Edition 2.0 | |
| IEC 60601-2-22 | EN-Medical electrical equipment - Part 2-22: Particular requirements for basic safety and essential performance of surgical cosmetic therapeutic and diagnostic laser equipment-Edition 3.0 | |
| IEC 60601-2-23 | EN-Medical Electrical Equipment - Part 2-23: Particular Requirements for the Safety Including Essential Performance of Transcutaneous Partial Pressure Monitoring Equipment-Second Edition | |
| IEC 60601-2-24 | EN-Medical Electrical Equipment - Part 2-24: Particular Requirements for the Safety of Infusion Pumps and Controllers-First Edition | |
| IEC 60601-2-25 | EN-Medical Electrical Equipment Part 2: Particular Requirements for the Safety of Electrocardiographs-First Edition; Amendment 1: 05-1999 | |
| IEC 60601-2-26 | EN-Medical Electrical Equipment Part 2-26: Particular Requirements for the Safety of Electroencephalographs-Second Edition | |
| IEC 60601-2-27 | EN-Medical electrical equipment - Part 2-27: Particular requirements for the safety including essential performance of electrocardiographic monitoring equipment-Second Edition | |
| IEC 60601-2-28 | EN-Medical electrical equipment - Part 2-28: Particular requirements for the basic safety and essential performance of X-ray tube assemblies for medical diagnosis-Edition 2.0 | |
| IEC 60601-2-29 | EN-Medical electrical equipment - Part 2-29: Particular requirements for the basic safety and essential performance of radiotherapy simulators-Third Edition | |
| IEC 60601-2-3 | EN-Medical Electrical Equipment Part 2: Particular Requirements for the Safety of Short-Wave Therapy Equipment-Second Edition; Amendment 1: 09-1998 | |
| IEC 60601-2-31 | EN-Medical electrical equipment - Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source-Edition 2.0 | |
| IEC 60601-2-32 | EN-Medical Electrical Equipment Part 2: Particular Requirements for the Safety of Associated Equipment of X-Ray Equipment-Edition 1.0; Also known as BS 5724: Section 2.32:1965; IEC 601-2-32:1994 | |
| IEC 60601-2-33 | EN-Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis-Edition 3.0 | |
| IEC 60601-2-34 | EN-Medical Electrical Equipment - Part 2-34: Particular Requirements for the Safety Including Essential Performance of Invasive Blood Pressure Monitoring Equipment-Edition 2 | |
| IEC 60601-2-36 | EN-Medical Electrical Equipment - Part 2: Particular Requirements for the Safety of Equipment for Extracorporeally Induced Lithotripsy-First Edition | |
| IEC 60601-2-37 | EN-IEC 60601-2-37 Edition 2.0 2007-08 Medical electrical equipment - Part 2-37: Particular requirements for the basic safety and essential performance of ultrasonic medical diagnostic and monitoring equipment-Edition | |
| IEC 60601-2-39 | EN-Medical electrical equipment - Part 2-39: Particular requirements for basic safety and essential performance of peritoneal dialysis equipment-Edition 2.0 | |
| IEC 60601-2-4 | EN-Medical Electrical Equipment Part 2-4: Particular Requirements for the Safety of Cardiac Defibrillators-Edition 2; Incorporates Corrigendum 04/2004 | |
| IEC 60601-2-40 | EN-Medical Electrical Equipment - Part 2-40: Particular Requirements for the Safety of Electromyographs and Evoked Response Equipment-First Edition | |
| IEC 60601-2-41 | EN-Medical electrical equipment - Part 2-41: Particular requirements for the basic safety and essential performance of surgical luminaires and luminaires for diagnosis-Edition 2.0 | |
| IEC 60601-2-43 | EN-Medical electrical equipment - Part 2-43: Particular requirements for the basic safety and essential performance of X-ray equipment for interventional procedures-Edition 2.0 | |
| IEC 60601-2-44 | EN-Medical electrical equipment - Part 2-44: Particular requirements for the basic safety and essential performance of X-ray equipment for computed tomography-Edition 3.0 | |
| IEC 60601-2-45 | EN-Medical electrical equipment - Part 2-45: Particular requirements for the safety of mammographic X-ray equipment and mammographic stereotactic devices-Edition 2 | |
| IEC 60601-2-46 | EN-Medical Electrical Equipment - Part 2-46: Particular Requirements for the Safety of Operating Tables-First Edition | |
| IEC 60601-2-47 | EN-Medical electrical equipment - Part 2-47: Particular requirements for the safety including essential performance of ambulatory electrocardiographic systems-Edition 1 | |
| IEC 60601-2-49 | EN-Medical electrical equipment - Part 2-49: Particular requirements for the safety of multifunction patient monitoring equipment-Edition 1 | |
| IEC 60601-2-5 | EN-Medical electrical equipment - Part 2-5: Particular requirements for the basic safety and essential performance of ultrasonic physiotherapy equipment-Edition 3.0 | |
| IEC 60601-2-50 | EN-Medical electrical equipment - Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment-Edition 2.0 | |
| IEC 60601-2-51 | EN-Medical electrical equipment Part 2-51: Particular requirements for safety including essential performance of recording and analysing single channel and multichannel electrocardiographs-Edition 1 | |
| IEC 60601-2-52 | EN-Medical electrical equipment - Part 2-52: Particular requirements for the basic safety and essential performance of medical beds-Edition 1.0 | |
| IEC 60601-2-54 | EN-Medical electrical equipment - Part 2-54: Particular requirements for the basic safety and essential performance of X-ray equipment for radiography and radioscopy-Edition 1.0 | |
| IEC 60601-2-6 | EN-Medical Electrical Equipment Part 2: Particular Requirements for the Safety of Microwave Therapy Equipment-First Edition; (NZS/AS 3200.2.6: 1992) | |
| IEC 60601-2-7 | EN-Medical Electrical Equipment - Part 2-7: Particular Requirements for the Safety of High-Voltage Generators of Diagnostic X-Ray Generators-Second Edition | |
| IEC 60601-2-8 | EN-Medical Electrical Equipment - Part 2-8: Particular Requirements for the Safety of Therapeutic X-Ray Equipment Operating in the Range 10 kV to 1 MV-Edition 1.1; Edition 1: 1987 Consolidated with Amendment 1: 1997 | |
| IEC 60601-3-1 | EN-Medical Electrical Equipment - Part 3-1: Essential Performance Requirements for Transcutaneous Oxygen and Carbon Dioxide Partial Pressure Monitoring Equipment-First Edition | |
| IEC 60613 | EN-Electrical and loading characteristics of X-ray tube assemblies for medical diagnosis-Edition 3.0 | |
| IEC 60627 | EN-Diagnostic X-Ray Imaging Equipment - Characteristics of General Purpose and Mammographic Anti-Scatter Grids-Second Edition; Replaces IEC 61953: 1997 | |
| IEC 60731 | EN-Medical Electrical Equipment - Dosimeters with Ionization Chambers as Used in Radiotherapy-Second Edition; Amendment 1 06-2002 | |
| IEC 60749-33 | EN-Semiconductor devices - Mechanical and climatic test methods - Part 33: Accelerated moisture resistance - Unbiased autoclave-First Edition; Replaces IEC PAS 62172:2000 | |
| IEC 60759 | EN-Standard Test Procedures for Semiconductor X-Ray Energy Spectrometers-Bilingual; First Edition; Amendment 1: 1991 | |
| IEC 60789 | EN-Medical electrical equipment - Characteristics and test conditions of radionuclide imaging devices - Anger type gamma cameras-Edition 3 | |
| IEC 60789 CORR 1 | EN-Medical electrical equipment - Characteristics and test conditions of radionuclide imaging devices - Anger type gamma cameras-Edition 3.0 |
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