Standards
Standards of EMC / EMI Laboratories
| International Electrotechnical Commission (IEC) | |
|---|---|
| IEC 801-2 | Electromagnetic compatibility for industrial-process measurement and control equipment. Part 2: Electrostatic discharge requirements |
| IEC 801-3 | Electromagnetic compatibility for industrial-process measurement and control equipment. Part 3: Radiated electromagnetic field requirements |
| IEC 801-4 | Electromagnetic compatibility for industrial-process measurement and control equipment. Part 4: Electrical fast transient & burst requirements |
| IEC 61000-4-2 | Electromagnetic compatibility (EMC) Part 4-2: Testing and measurement techniques – Electrotatic discharge immunity test |
| IEC 61000-4-3 | Electromagnetic compatibility (EMC) Part 4-3: Testing and measurement techniques – Radiated, radio frequency, electromagnetic field immunity test |
| IEC 61000-4-4 | Electromagnetic compatibility (EMC) Part 4-4: Testing and measurement techniques – Electrical fast transient/burst immunity test |
| IEC 61000-4-5 | Electromagnetic compatibility (EMC) Part 4-5: Testing and measurement techniques – Surge immunity test |
| IEC 61000-4-6 | Electromagnetic compatibility (EMC) Part 4-6: Testing and measurement techniques – Immunity to conducted disturbances, induced by radio-frequency fields |
| IEC 61000-4-8 | Electromagnetic compatibility (EMC) Part 4-8: Testing and measurement techniques – Power frequency magnetic field. Immunity test |
| IEC 61000-4-11 | Electromagnetic compatibility (EMC) Part 4-11 : Testing and measurement techniques – Voltage dips, short interruptions and voltage variations immunity tests |
| IEC 61000-3-2 | Electromagnetic compatibility (EMC) Part 3-2: Limits for harmonic current emissions (equipment input current up to 16 A per phase) |
| IEC 61000-3-3 | Electromagnetic compatibility (EMC) Part 3-3: Limitation of voltage fluctuations and flicker in low-voltage supply systems for equipment with rated current above 16 A |
| IEC 60601-1-2 | Medical electrical equipment. Part 1-2: General requirements for safety. Collateral Standard: Electromagnetic compatibility – Requirements and tests |
| IEC/CISPR 11 | Insdustrial, scientific and medical (ISM) radio-frequency equipment - Electromagnetic disturbance characteristics – Limits and methods of measurement |
| IEC/CISPR 14-1 | Electromagnetic compatibility Requirements for household appliances, electric tools and similiar apparatus Part 1: Emission |
| IEC/CISPR 14-2 | Electromagnetic compatibility Requirements for household appliances, electric tools and similar apparatus Part 2: Immunity – Product family standard |
| IEC/CISPR 22 | Information technology equipment Radio disturbance characteristics – Limits and methods of measurement |
| IEC/CISPR 24 | Information technology equipment Immunity characteristics – Limits and methods of measurement |
| International Telecommunication Union (ITU) | |
| ITU-T Rec. k.20 | Resistibility of telecommunications equipment installed in a telecommunications centre to over voltages and over currents |
| ITU-T Rec. k.21 | Resistibility of Telecommunications equipment installed in customer premises to over voltages and overcurrents. |
| ITU-T Rec. k.22 | Over voltage resistibility of equipment connected to an ISDN T/S bus. |
| ITU-T Rec. k.38 | Radiated emission test procedure for physically large systems |
| Federal Communications Commission (FCC) | |
| FCC Part 15 | Radio Frequency Devices |
| American National Standards Institute (ANSI) | |
| ANSI C63.4 | Standard for Methods of Measurement of Radio-Noise - Emissions from Low-Voltage - Electrical and Eletronic Equipment in the Range of 9 kHz to 40 GHz |
| ANSI C63.5 | American national standard for calibration of antennas used for radiated emission measurements in electromagnetic interference (EMI) control |
| Normas Européias (EN) | |
| EN 55011 | Limits and methods of measurement of radio disturbance characteristics of industrial, scientific and medical (ISM) radio frequency equipment (CISPR 11 modified) |
| EN 55022 | Information technology equipment – Radio disturbance characteristics. Limits and methods of measurement (CISPR 22 modified) |
| INMETRO directives | |
| Directive n.º 006/2002 | Metrological and technical conditions applied to portable and non-portable alcohol monitors. |
| Directive n.º 115/1998 | Metrological and technical conditions applied to speed monitors for automotive vehicles. |
| Directive n.º 201/2002 | Metrological and technical conditions applied to Taximeters. |
| Directive n.º 201/2004 | Metrological and technical conditions applied to Chrono-tacographs. |
| Directive n.º 236/1994 | Metrological and technical conditions applied to non-automated weighing instruments. |
| Directive n.º 431/2007 | Metrological and technical conditions applied to Elelctronic Measurers of Electric Power. |
| ANATEL Resolutions | |
| Resolution n.° 442 | Regulation for the certification of telecommunication equipments regarding electromagnetic compatibility aspects |
| Resolution n.° 529 | Regulation for the certification of telecommunication equipments regarding electrical safety aspects |
| Resolution n.° 506 | Regulation for radio-communication equipments with restricted radiation |
| Resolution n.° 473 | Regulation of user-network interface and public switched telephone service terminals |
| Resolution n.° 416 | Regulation of conditions for using the the 3,5 GHz radio frequency band |
| ABNT / NBR Standards | |
| NBR 12304 | Limits and measurement methods for radio-perturbation in Information Technology Equipments (ITE) |
| NBR IEC/CISPR 11 | Industrial, scientific and medical (ISM) radio-frequency equipment – Electromagnetic disturbance characteristics – Limits and methods of measurement) |
| NBR IEC 60601-1 | Medical Electrical Equipment Part 1: General requirements for safety |
| NBR IEC 60601-1-1 | Medical Electrical Equipment Parte 1: General requirements for safety Collateral Standard: Safety requirements for medical electrical systems |
| NBR IEC 60601-1-2 | Medical Electrical Equipment Parte 1: General requirements for safety 2. Collateral Standard: Electromagnetic Compatibility - requirements and tests |
| NBR IEC 60601-2-2 | Medical Electrical Equipment Part 2-2: Particular requirements for the safety of high frequency surgical equipment |
| NBR IEC 60601-2-3 | Medical Electrical Equipmen Part 2-3: Particular requirements for the safety of short-wave therapy equipment |
| NBR IEC 60601-2-5 | Medical Electrical Equipment Particular requirements for the safety of ultrasonic physiotherapy equipment |
| NBR IEC 60601-2-6 | Medical Electrical Equipment Particular requirements for the safety of microwave therapy equipment |
| NBR IEC 60601-2-7 | Medical Electrical Equipment Parte 2-7: Particular requirements for the safety of high-voltage generators of diagnostic X-Ray |
| NBR IEC 60601-2-10 | Medical Electrical Equipment Part 2-10: Particular requirements for the safety of nerve and muscle stimulators |
| NBR IEC 60601-2-12 | Medical Electrical Equipment Part 2-12: Particular requirements for the safety of lung ventilators for medical use |
| NBR IEC 60601-2-13 | Medical Electrical Equipment Part 2-13: Particular requirements for the safety of anaesthetic workstations |
| NBR IEC 60601-2-14 | Medical Electrical Equipment Part 2-14: Particular requirements for the safety of electroconvulsive therapy equipment |
| NBR IEC 60601-2-16 | Medical Electrical Equipment Part 2-16:Particular requirements for the safety of Haemodialysis equipment |
| NBR IEC 60601-2-18 | Medical Electrical Equipment Part 2-18: Particular requirements for the safety of endoscopic equipment |
| NBR IEC 60601-2-19 | Medical Electrical Equipment Part 2-19: Particular requirements of safety of baby incubators |
| NBR IEC 60601-2-20 | Medical Electrical Equipment Part 2-20: Particular requirements for the safety of transport incubators |
| NBR IEC 60601-2-21 | Medical Electrical Equipment Part 2-21: Particular requirements for the safety of infant radiant warmers |
| NBR IEC 60601-2-22 | Medical Electrical Equipment Part 2-22: Particular requirements for the safety of diagnostic and therapeutic laser equipment |
| NBR IEC 60601-2-24 | Medical Electrical Equipment Part 2-24: Particular requirements for the safety of infusion pumps and controllers |
| NBR IEC 60601-2-25 | Medical Electrical Equipment Part 2-25: Particular requirements for the safety of electrocardiographs |
| NBR IEC 60601-2-26 | Medical Electrical Equipment Part 2-26: Particular requirements for the safety of eletcroencephalographs |
| NBR IEC 60601-2-27 | Medical Electrical Equipment Part 2-27: Particular requirements for the safety of electrocardiographic monitoring equipment/td> |
| NBR IEC 60601-2-28 | Medical Electrical Equipment Part 2-28: Particular requirements for the safety of x-ray source assemblies and x-ray tube assemblies for medical diagnosis |
| NBR IEC 60601-2-30 | Medical Electrical Equipment Part 2-30: Particular requirements for the safety of automatic cycling non-invasive blood pressure monitoring equipment |
| NBR IEC 60601-2-31 | Medical Electrical Equipment Part 2-31: Particular requirements for the safety of external cardiac pacemakers with internal power source |
| NBR IEC 60601-2-32 | Medical Electrical Equipment Part 2-32: Particular requirements for the safety of associated equipment of x-ray equipment |
| NBR IEC 60601-2-34 | Medical Electrical Equipment Part 2-34: Particular requirements for the safety of invasive blood pressure monitoring systems |
| NBR IEC 60601-2-37 | Medical Electrical Equipment Part 2-37: Particular requirements for the safety of ultrasonic medical diagnosic and monitoring equipment |
| NBR IEC 60601-2-38 | Medical Electrical Equipment Part 2-38: Particular requirements for the safety of electrically operated hospital beds |
| NBR IEC 60601-2-40 | Medical Electrical Equipment Part 2-40: Particular requirements for the safety of electromyographs and evoked response equipment |
| NBR IEC 60601-2-46 | Medical Electrical Equipment Part 2-46: Particular requirements for the safety of operating tables |
| NBR IEC 60601-2-47 | Medical Electrical Equipment Part 2-47: Particular requirements for the safety, including essential performance, of ambulatory electrocardiographic systems |
| NBR IEC 60601-2-49 | Medical Electrical Equipment Part 2-49: Particular requirements for the safety of multifunction patient monitoring equipment |
| NBR IEC 60601-2-50 | Medical Electrical Equipment Part 2-50: Particular requirements for the safety of infant phototerapy equipment |