EUROFILE - Administration/Test and Measurement Collection
This collection contains documents from the following standards organization(s): European Committee for Standardization, European Committee for Electrotechnical Standardization
| CENELEC EN 60450 | EN-Measurement of the average viscometric degree of polymerization of new and aged cellulosic electrically insulating materials-Incorporates Amendment A1: 2007 | |
| CENELEC EN 60454-2 | EN-Pressure-sensitive adhesive tapes for electrical purposes - Part 2: Methods of test | |
| CENELEC EN 60464-2 | EN-Varnishes used for electrical insulation Part 2: Methods of test-Incorporating Amendment A1: 03/2006 and Corrigendum: 12/2006 | |
| CENELEC EN 60464-2 | EN-Varnishes Used for Electrical Insulation - Part 2: Methods of Test-Includes amendment A1:2006; IEC 60464-2: 2001 + A1:2006; | |
| CENELEC EN 60477 | EN-Laboratory d.c. Resistors-Incorporates Amendment A1: 1997 | |
| CENELEC EN 60477-2 | EN-Laboratory Resistors - Part 2: Laboratory a.c. Resistors-Incorporates Amendment A1: 1997 | |
| CENELEC EN 60514 | EN-Acceptance Inspection of Class 2 Alternating- Current Watthour Meters | |
| CENELEC EN 60522 | EN-Determination of the Permanent Filtration of X-Ray Tube Assemblies-IEC 60522: 1999 | |
| CENELEC EN 60523 | EN-Direct-Current Potentiometers-Incorporates Amendment A2: 1997 | |
| CENELEC EN 60524 | EN-Direct-Current Resistive Volt Ratio Boxes-Incorporates Amendment A2: 1997 | |
| CENELEC EN 60526 | EN-High-voltage cable plug and socket connections for medical X-ray equipment-IEC 60526:1978 modified; Supersedes HD 364 S2:1983 | |
| CENELEC EN 60534-4 | EN-Industrial-process control valves Part 4: Inspection and routine testing-IEC 60534-4:2006 | |
| CENELEC EN 60534-8-1 | EN-Industrial-process control valves Part 8-1: Noise considerations - Laboratory measurement of noise generated by aerodynamic flow through control valves | |
| CENELEC EN 60534-8-3 | EN-Industrial-Process Control Valves Part 8-3: Noise Considerations - Control Valve Aerodynamic Noise Prediction Method-IEC 60534-8-3: 2000 | |
| CENELEC EN 60534-8-4 | EN-Industrial-process control valves Part 8-4: Noise considerations - Prediction of noise generated by hydrodynamic flow | |
| CENELEC EN 60544-4 | EN-Electrical insulating materials - Determination of the effects of ionizing radiation Part 4: Classification system for service in radiation environments-IEC 60544-4:2003 | |
| CENELEC EN 60544-5 | EN-Electrical insulating materials Determination of the effects of ionizing radiation Part 5: Procedures for assessment of ageing in service-IEC 60544-5:2003 | |
| CENELEC EN 60554-2 | EN-Cellulosic Papers for Electrical Purposes - Part 2: Methods of Test-IEC 60554-2:2001 | |
| CENELEC EN 60564 | EN-D.C. Bridges for Measuring Resistance-Includes Amendment A2: 1997; IEC 564: 1977 + A1: 1981 and A2: 1997; Supersedes HD 615 S1: 1992 | |
| CENELEC EN 60565 | EN-Underwater acoustics - Hydrophones - Calibration in the frequency range 0 1 Hz to 1 MHz | |
| CENELEC EN 60567 | EN-Oil-filled electrical equipment - Sampling of gases and of oil for analysis of free and dissolved gases - Guidance-(IEC 60567):2005 | |
| CENELEC EN 60580 | EN-Medical Electrical Equipment Dose Area Product Meters-Supersedes HD 379 S1: 1979; IEC 60580: 2000 | |
| CENELEC EN 60584-1 | EN-Thermocouples Part 1: Reference Tables (IEC 584-1 : 1995) | |
| CENELEC EN 60584-2 | EN-Thermocouples Part 2: Tolerances (IEC 584-2 : 1982 + A1: 1989) | |
| CENELEC EN 60584-3 | EN-Thermocouples - Part 3: Extension and compensating cables - Tolerances and identification system | |
| CENELEC EN 60587 | EN-Electrical insulating materials used under severe ambient conditions - Test methods for evaluating resistance to tracking and erosion | |
| CENELEC EN 60599 | EN-Mineral Oil-Impregnated Electrical Equipment in Service - Guide to the Interpretation of Dissolved and Free Gases Analysis-Incorporated Amendment A1: May 2007 | |
| CENELEC EN 60601-1 | EN-Medical Electrical Equipment Part 1: General Requirements for Basic Safety and Essential Performance | |
| CENELEC EN 60601-1-1 | EN-Medical Electrical Equipment Part 1-1: General Requirements for Safety Collateral Standard: Safety Requirements for Medical Electrical Systems-IEC 60601-1-1:2000 | |
| CENELEC EN 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 | |
| CENELEC EN 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 in th | |
| CENELEC EN 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-Incorporating corrigendum March 2 | |
| CENELEC EN 60601-1-3 | EN-Medical electrical equipment - Part 1-3: General requirements for basic safety and essential performance - Collateral Standard: Radiation protection in diagnostic X-ray equipment-Incorporating corrigendum March 2010 | |
| CENELEC EN 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 (IEC 601-1-3:1994)-Remains Current | |
| CENELEC EN 60601-1-4 | EN-Medical Electrical Equipment - Part 1-4: General Requirements for Safety - Collateral Standard: Programmable Electrical Medical Systems-Includes Amendment A1:1999; IEC 60601-1-4:1996 + A1:1999 | |
| CENELEC EN 60601-1-6 | EN-Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability | |
| CENELEC EN 60601-1-6 | EN-Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral Standard: Usability-Remains Current | |
| CENELEC EN 60601-1-8 | EN-Medical electrical equipment Part 1-8: General requirements for safety - Collateral standard: General requirements tests and guidance for alarm systems in medical electrical equipment and medical electrical systems- | |
| CENELEC EN 60601-1-8 | EN-Medical electrical equipment Part 1-8: General requirements for safety - Collateral standard: General requirements tests and guidance for alarm systems in medical electrical equipment and medical electrical systems- | |
| CENELEC EN 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 equipme | |
| CENELEC EN 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 | |
| CENELEC EN 60601-2-1 | EN-Medical Electrical Equipment - Part 2-1: Particular Requirements for the Safety of Electron Accelerators in the Range of 1 MeV to 50 MeV-Includes Amendment A1:2002; IEC 60601-2-1:1998 + A1:2002 | |
| CENELEC EN 60601-2-10 | EN-Medical electrical equipment Part 2-10: Particular requirements for the safety of nerve and muscle stimulators-Includes amendment A1: 2001; IEC 60601-2-10: 1987 + A1: 2001; Supersedes HD 395.2.10 S1: 1989 | |
| CENELEC EN 60601-2-11 | EN-Medical Electrical Equipment Part 2: Particular Requirements for the Safety of Gamma Beam Therapy Equipment-IEC 601-2-11: 1997 + A1:2004; Supersedes HD 395.2.11 S2:1990; Includes Amendment A1:2004 | |
| CENELEC EN 60601-2-12 | EN-Medical electrical equipment Part 2-12: Particular requirements for the safety of lung ventilators Critical care ventilators-IEC 60601-2-12:2001 | |
| CENELEC EN 60601-2-13 | EN-Medical electrical equipment Part 2-13: Particular requirements for the safety and essential performance of anaesthetic systems-Incorporates amendment A1: 03/2007 | |
| CENELEC EN 60601-2-16 | EN-Medical Electrical Equipment Part 2-16: Particular Requirements for the Safety of Haemodialysis Haemodiafiltration and Haemofiltration Equipment-Supersedes HD 395.2.16 S1:1989; Incorporating Corrigendum: December 19 | |
| CENELEC EN 60601-2-17 | EN-Medical electrical equipment Part 2-17: Particular requirements for the safety of automatically-controlled brachytherapy afterloading equipment-IEC 60601-2-17:2004 | |
| CENELEC EN 60601-2-18 | EN-Medical electrical equipment Part 2: Particular requirements for the safety of endoscopic equipment-Includes amendment A1: 2000; IEC 60601-2-18: 1996 + A1: 2000 | |
| CENELEC EN 60601-2-19 | EN-Medical electrical equipment - Part 2-19: Particular requirements for the basic safety and essential performance of infant incubators | |
| CENELEC EN 60601-2-2 | EN-Medical Electrical Equipment Part 2-2: Particular Requirements for the Safety of High Frequency Surgical Equipment-IEC 60601-2-2:1998 | |
| CENELEC EN 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 | |
| CENELEC EN 60601-2-20 | EN-Medical electrical equipment - Part 2-20: Particular requirements for the basic safety and essential performance of infant transport incubators | |
| CENELEC EN 60601-2-20 | EN-Medical Electrical Equipment; Part 2: Particular Requirements for the Safety of Transport Incubators-Supersedes HD 395.2.19 S1: 1992; IEC 601-2-20: 1990 + A1 : 1996; Remains Current | |
| CENELEC EN 60601-2-21 | EN-Medical electrical equipment - Part 2-21: Particular requirements for the basic safety and essential performance of infant radiant warmers | |
| CENELEC EN 60601-2-22 | EN-Medical Electrical Equipment - Part 2: Particular Requirements for the Safety of Diagnostic and Therapeutic Laser Equipment (IEC 601-2-22: 1995) | |
| CENELEC EN 60601-2-23 | EN-Medical Electrical Equipment Part 2: Particular Requirements for the Safety Including Essential Performance of Transcutaneous Partial Pressure Monitoring Equipment-IEC 60601-2-23:1999 | |
| CENELEC EN 60601-2-24 | EN-Medical Electrical Equipment Part 2: Particular Requirements for the Safety of Infusion Pumps and Controllers | |
| CENELEC EN 60601-2-25 | EN-Medical Electrical Equipment - Part 2-25: Particular Requirements for the Safety of Electrocardiographs-Includes Amendment A1: 1999; IEC 60601-2-25: 1993 + A1: 1999 | |
| CENELEC EN 60601-2-26 | EN-Medical electrical equipment Part 2-26: Particular requirements for the safety of electroencephalographs-IEC 60601-2-26: 2002 | |
| CENELEC EN 60601-2-27 | EN-Medical electrical equipment Part 2-27: Particular requirements for the safety including essential performance of electrocardiographic monitoring equipment-Incorporating Corrigendum December 2006 | |
| CENELEC EN 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 (IEC 601-2-28 : 1993)-Remains Current | |
| CENELEC EN 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 | |
| CENELEC EN 60601-2-29 | EN-Medical electrical equipment - Part 2-29: Particular requirements for the basic safety and essential performance of radiotherapy simulators | |
| CENELEC EN 60601-2-3 | EN-Medical electrical equipment Part 2. Particular requirements for the safety of short-wave therapy equipment-Supersedes HD 395.2.3 S1:1985; Includes amendment A1:1998; IEC 60601-2-3:1991 + A1:1998 | |
| CENELEC EN 60601-2-30 | EN-Medical Electrical Equipment Part 2-30: Particular Requirements for the Safety Including Essential Performance of Automatic Cycling Non-Invasive Blood Pressure Monitoring Equipment-IEC 60601-2-30: 1999 | |
| CENELEC EN 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 | |
| CENELEC EN 60601-2-33 | EN-Medical electrical equipment - Part 2-33: Particular requirements for the safety of magnetic resonance equipment for medical diagnosis-Incorporates Amendment A2: March 2008 | |
| CENELEC EN 60601-2-34 | EN-Medical Electrical Equipment Part 2-34: Particular Requirements for the Safety Including Essential Performance of Invasive Blood Pressure Monitoring Equipment-IEC 60601-2-34:2000 | |
| CENELEC EN 60601-2-36 | EN-Medical Electrical Equipment Part 2: Particular Requirements for the Safety of Equipment for Extracorporeally Induced Lithotripsy-IEC 60601-2-36: 1997 | |
| CENELEC EN 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 | |
| CENELEC EN 60601-2-39 | EN-Medical electrical equipment - Part 2-39: Particular requirements for basic safety and essential performance of peritoneal dialysis equipment | |
| CENELEC EN 60601-2-4 | EN-Medical electrical equipment Part 2-4: Particular requirements for the safety of cardiac defibrillators-IEC 60601-2-4: 2002; Supersedes HD 395.2.4 S1: 1988 | |
| CENELEC EN 60601-2-40 | EN-Medical Electrical Equipment Part 2-40: Particular Requirements for the Safety of Electromyographs and Evoked Response Equipment-IEC 60601-2-40:1998 | |
| CENELEC EN 60601-2-41 | EN-Medical electrical equipment - Part 2-41: Particular requirements for basic safety and essential performance of surgical luminaires and luminaires for diagnosis | |
| CENELEC EN 60601-2-41 | EN-Medical electrial equipment Part 2-41: Particular Requirements for the Safety of Surgical Iuminaires and Luminaires for Diagnosis-IEC 60601-2-41:2000; Remains Current | |
| CENELEC EN 60601-2-43 | EN-Medical electrical equipment - Part 2-43: Particular requirements for basic safety and essential performance of X-ray equipment for interventional procedures | |
| CENELEC EN 60601-2-43 | EN-Medical Electrical Equipment Part 2-43: Particular Requirements for the Safety of X-Ray Equipment for Interventional Procedures-IEC 60601-2-43:2000; Remains Current | |
| CENELEC EN 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 |