IEC Special Cllection TH Collection
This collection contains documents from the following standards organization(s): Union Technique de I.Electricite 1 2 3 > >
| UTE IEC CEI 60050-891 | EN-International Electrotechnical Vocabulary Part 891: Electrobiology | |
| UTE IEC CEI 60336 | EN-Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Characteristics of focal spots | |
| UTE IEC CEI 60336/AC1 | EN-Medical electrical equipment - X-ray tube assemblies for medical diagnosis - Characteristics of focal spots | |
| UTE IEC CEI 60513 | EN-Fundamental aspects of safety standards for medical electrical equipment | |
| UTE IEC CEI 60601-1-1 | EN-Medical electrical equipment - Part 1-1: General requirements for safety - Collateral standard: Safety requirements for medical electrical systems | |
| UTE IEC CEI 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 | |
| UTE IEC CEI 60601-1-3 | EN-Part 1-3: General requirements for basic safety and essential performance - Collateral Standard: Radiation protection in diagnostic X-ray equipment | |
| UTE IEC CEI 60601-1-4 COMPIL | EN-Medical electrical equipment - Part 1-4: General requirements for safety - Collateral standard: Programmable electrical medical systems-Consolidated Reprint | |
| UTE IEC CEI 60601-1-4/A1 | EN-Medical electrical equipment - Part 1-4: General requirements for safety - Collateral standard: Programmable electrical medical systems | |
| UTE IEC CEI 60601-1-6 | EN-Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral Standard: Usability | |
| UTE IEC CEI 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 equipm | |
| UTE IEC CEI 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 | |
| UTE IEC CEI 60601-1-F1 | EN-MEDICAL ELECTRICAL EQUIPMENT - Part 1: General requirements for basic safety and essential performance INTERPRETATION SHEET 1 | |
| UTE IEC CEI 60601-1/AC2 | EN-Medical electrical equipment - Part 1: General requirements for basic safety and essential performance | |
| UTE IEC CEI 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 | |
| UTE IEC CEI 60601-2-10 | EN-Medical electrical equipment - Part 2 : particular requirements for the safety of nerve and muscle stimulators | |
| UTE IEC CEI 60601-2-10/A1 | EN-Amendment 1 to publication IEC 60601-2-10:1987 | |
| UTE IEC CEI 60601-2-10/A1/AC1 | EN-Medical electrical equipment. Part 2-10: Particular requirements for the safety of nerve and muscle stimulators Amendment 1; CORRIGENDUM 1 | |
| UTE IEC CEI 60601-2-11 | EN-Medical electrical equipment - Part 2: Particular requirements for the safety of gamma beam therapy equipment | |
| UTE IEC CEI 60601-2-11/A1 | EN-Medical electrical equipment - Part 2-11: Particular requirements for the safety of gamma beam therapy equipment | |
| UTE IEC CEI 60601-2-12 | EN-Medical electrical equipment - Part 2-12 : particular requirements for the safety of lung ventilators - Critical care ventilators | |
| UTE IEC CEI 60601-2-13 | EN-Medical electrical equipment - Part 2-13: particular requirements for the safety and essential performance of anaesthetic systems | |
| UTE IEC CEI 60601-2-13 COMPIL | EN-Medical electrical equipment - Part 2-13: Particular requirements for the safety and essential performance of anaesthetic systems-Consolidated Reprint | |
| UTE IEC CEI 60601-2-13/A1 | EN-Medical electrical equipment - Part 2-13: particular requirements for the safety and essential performance of anaesthetic systems | |
| UTE IEC CEI 60601-2-16 | EN-Medical electrical equipment - Part 2-16: Particular requirements for basic safety and essential performance of haemodialysis haemodiafiltration and haemofiltration equipment | |
| UTE IEC CEI 60601-2-16/AC1 | EN-Medical electrical equipment - Part 2-16: Particular requirements for basic safety and essential performance of haemodialysis haemodiafiltration and haemofiltration equipment | |
| UTE IEC CEI 60601-2-17 | EN-Medical electrical equipment - Part 2-17: Particular requirements for the safety of automatically-controlled brachytherapy afterloading equipment | |
| UTE IEC CEI 60601-2-18 | EN-Medical electrical equipment - Part 2-18: Particular requirements for the basic safety and essential performance of endoscopic equipment | |
| UTE IEC CEI 60601-2-19 | EN-Medical electrical equipment - Part 2-19: Particular requirements for the basic safety and essential performance of infant incubators | |
| UTE IEC CEI 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 | |
| UTE IEC CEI 60601-2-20 | EN-Medical electrical equipment - Part 2-20: Particular requirements for the basic safety and essential performance of infant transport incubators | |
| UTE IEC CEI 60601-2-21 | EN-Medical electrical equipment - Part 2-21: Particular requirements for the basic safety and essential performance of infant radiant warmers | |
| UTE IEC CEI 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 | |
| UTE IEC CEI 60601-2-23 | EN-Medical electrical equipment - Part 2-23: Particular requirements for the safety including essential performance of transcutaneous partial pressure monitoring equipment | |
| UTE IEC CEI 60601-2-24 | EN-Medical electrical equipment - Part 2-24: Particular requirements for the safety of infusion pumps and controllers | |
| UTE IEC CEI 60601-2-25 | EN-Medical electrical equipment - Part 2: Particular requirements for the safety of electrocardiographs | |
| UTE IEC CEI 60601-2-25/A1 | EN-Medical electrical equipment - Part 2-25: Particular requirements for the safety of electrocardiographs | |
| UTE IEC CEI 60601-2-26 | EN-Medical electrical equipment - Part 2-26: Particular requirements for the safety of electroencephalographs | |
| UTE IEC CEI 60601-2-27 | EN-Medical electrical equipment - Part 2-27: Particular requirements for the safety including essential performance of electrocardiographic monitoring equipment | |
| UTE IEC CEI 60601-2-28 | EN-Medical electrical equipment - Part 2: Particular requirements for the safety of X-ray source assemblies and X-ray tube assemblies for medical diagnosis | |
| UTE IEC CEI 60601-2-29 | EN-Medical electrical equipment - Part 2-29: Particular requirements for the basic safety and essential performance of radiotherapy simulators | |
| UTE IEC CEI 60601-2-3 | EN-Medical Electrical Equipment Part 2: Particular Requirements for the Safety of Short-Wave Therapy Equipment | |
| UTE IEC CEI 60601-2-3/A1 | EN-Medical Electrical Equipment Part 2: Particular Requirements for the Safety of Short-Wave Therapy Equipment | |
| UTE IEC CEI 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 | |
| UTE IEC CEI 60601-2-32 | EN-Medical electrical equipment - Part 2: Particular requirements for the safety of associated equipment of X-ray equipment | |
| UTE IEC CEI 60601-2-33 | EN-Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis | |
| UTE IEC CEI 60601-2-33 COMPIL | EN-Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis-Consolidated Reprint | |
| UTE IEC CEI 60601-2-33/A1 | EN-Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis | |
| UTE IEC CEI 60601-2-33/A2 | EN-Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis | |
| UTE IEC CEI 60601-2-34 | EN-Medical electrical equipment - Part 2-34: Particular requirements for the safety including essential performance Of invasive blood pressure monitoring equipment | |
| UTE IEC CEI 60601-2-36 | EN-Medical electrical equipment - Part 2: Particular requirements for the safety of equipment for extracorporeally induced lithotripsy | |
| UTE IEC CEI 60601-2-37 | EN-Medical electrical equipment - Part 2-37: Particular requirements for the basic safety and essential performance of ultrasonic medical diagnostic and monitoring equipment | |
| UTE IEC CEI 60601-2-39 | EN-Medical electrical equipment - Part 2-39: Particular requirements for basic safety and essential performance of peritoneal dialysis equipment | |
| UTE IEC CEI 60601-2-4 | EN-Medical electrical equipment - Part 2-4: Particular requirements for the safety of cardiac defibrillators | |
| UTE IEC CEI 60601-2-40 | EN-Medical electrical equipment - Part 2-40: Particular requirements for the safety electromyographs and evoked response equipment | |
| UTE IEC CEI 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 | |
| UTE IEC CEI 60601-2-43 | EN-Medical electrical equipment - Part 2-43: Particular requirements for the safety of X-ray equipment for interventional procedures | |
| UTE IEC CEI 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 | |
| UTE IEC CEI 60601-2-45 | EN-Medical electrical equipment - Part 2-45: Particular requirements for the safety of mammographic X-ray equipment and mammographic stereotactic devices | |
| UTE IEC CEI 60601-2-47 | EN-Medical electrical equipment - Part 2-47: Particular requirements for the safety including essential performance of ambulatory electrocardiographic systems | |
| UTE IEC CEI 60601-2-49 | EN-Medical electrical equipment - Part 2-49: Particular requirements for the safety of multifunction patient monitoring equipment | |
| UTE IEC CEI 60601-2-5 | EN-Medical electrical equipment - Part 2-5: Particular requirements for the basic safety and essential performance of ultrasonic physiotherapy equipment | |
| UTE IEC CEI 60601-2-50 | EN-Medical electrical equipment - Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment | |
| UTE IEC CEI 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 | |
| UTE IEC CEI 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 | |
| UTE IEC CEI 60601-2-6 | EN-Medical Electrical Equipment Part 2: Particular Requirements for the Safety of Microwave Therapy Equipment | |
| UTE IEC CEI 60601-2-7 | EN-Medical electrical equipment - Part 2-7: Particular requirements for the safety of high-voltage generators of diagnostic X-ray generators | |
| UTE IEC CEI 60601-2-8 COMPIL | 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-Consolidated Reprint | |
| UTE IEC CEI 60601-2-8/A1 | EN-Medical electrical equipment - Part 2: Particular requirements for the safety of therapeutic X-ray equipment operating in the range 10 kV to 1 MV | |
| UTE IEC CEI 60601-2-9 | EN-Medical electrical equipment - Part 2: Particular requirements for the safety of patient contact dosemeters used in radiotherapy with electrically connected radiation detectors | |
| UTE IEC CEI 60601-3-1 | EN-Medical electrical equipment - Part 3-1: Essential performance requirements for transcutaneous oxygen and carbon dioxide partial pressure monitoring equipment | |
| UTE IEC CEI 60613 | EN-Electrical Thermal and Loading Characteristics of Rotating Anode X-Ray Tubes for Medical Diagnosis | |
| UTE IEC CEI 60627 | EN-Diagnostic X-ray imaging equipment - Characteristics of general purpose and mammographic anti-scatter grids | |
| UTE IEC CEI 60731 | EN-Medical electrical equipment - Dosimeters with ionization chambers as used in radiotherapy | |
| UTE IEC CEI 60731/A1 | EN-Medical electrical equipment - Dosimeters with ionization chambers as used in radiotherapy | |
| UTE IEC CEI 60789 | EN-Medical electrical equipment - Characteristics and test conditions of radionuclide imaging devices - Anger type gamma cameras | |
| UTE IEC CEI 60806 | EN-Determination of the Maximum Symmetrical Radiation Field from a Rotating Anode X-Ray Tube for Medical Diagnosis | |
| UTE IEC CEI 60854 | EN-Methods of Measuring the Performance of Ultrasonic Pulse-Echo Diagnostic Equipment | |
| UTE IEC CEI 61010-2-101 | EN-Safety requirements for electrical equipment for measurement control and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment |
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