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[12/160F21] RTCA/DO-160F (2007)
Environmental Conditions and Test Procedures for Airborne Equipment - Section 21 - Emissions of Radio Frequency Energy
[12/CIS11h] AS/NZS CISPR 11 (2004)
Industrial, scientific and medical (ISM) radio frequency equipment - Electromagnetic disturbance characteristics - Limits and methods of measurement
[12/CIS11m1] EN 55011:2009
Industrial, scientific and medical equipment. Radio-frequency disturbance characteristics. Limits and methods of measurement
[12/CIS11pp] IEC/CISPR 11 Ed 5 (2009-05) + A1 (2010)
Industrial, scientific and medical equipment - Radio-frequency disturbance characteristics - Limits and methods of measurement
[12/CIS22j] EN 55022 (2006)
Information technology equipment - Radio disturbance characteristics - Limits and methods of measurement
[12/CIS22k] IEC/CISPR 22 (2008-09)
Limits and Methods of Measurement of Radio Disturbance Characteristics of Information Technology Equipment
[Z500013-E1] Exclusions
CISPR 11 and CISPR 22 - Conducted Emissions only
[12/I01d] IEC 61000-4-2, Ed. 2.0 (2008-12)
Electromagnetic compatibility (EMC) - Part 4-2: Testing and measurement techniques - Electrostatic discharge immunity test
[12/I01f] EN 61000-4-2 (2009-05)
Electromagnetic compatibility (EMC) — Part 4-2 : Testing and measurement techniques — Electrostatic discharge immunity test
[12/I02h] EN 61000-4-3 (2006)
Radiated, radio-frequency, electromagnetic field immunity test
[12/I02i1] IEC 61000-4-3 Ed. 3.2 (2010)
Electromagnetic compatibility (EMC) - Part 4-3: Testing and measurement techniques - Radiated, radio-frequency, electromagnetic field immunity test
[12/I03e] EN 61000-4-4 (2004)
Electromagnetic compatibility (EMC) - Part 4-4: Testing and measurement techniques - Electrical fast transient/burst immunity test
[12/I03g] IEC 61000-4-4, Ed. 2.0 + A1 (2010)
Electromagnetic compatibility (EMC) - Part 4-4: Testing and measurement techniques - Electrical Fast Transient/Burst Immunity Test
[12/I04c1] IEC 61000-4-5, Ed 2 (2005-11)
EMC - Part 4-5: Testing and measurement techniques - Surge immunity test
[12/I04d] BS EN 61000-4-5 (2006)
Electromagnetic compatibility (EMC). Testing and measurement techniques. Surge immunity test
[12/I05f1] IEC 61000-4-6 Ed. 3.0 (2008)
Electromagnetic compatibility (EMC) - Part 4-6: Testing and measurement techniques - Immunity to conducted disturbances, induced by radio-frequency fields
[12/I05j] EN 61000-4-6 (2009)
Electromagnetic compatibility (EMC) - Part 4-6: Testing and measurement techniques - Immunity to conducted disturbances, induced by radio-frequency fields
[12/I06e] IEC 61000-4-8 (2009)
Electromagnetic compatibility (EMC) - Part 4-8: Testing and measurement techniques - Power frequency magnetic field immunity test
[12/I06f] EN 61000-4-8:2010
Electromagnetic compatibility (EMC). Testing and measurement techniques. Power frequency magnetic field immunity test
[12/I07f] EN 61000-4-11 (2004)
Voltage Dips, Short Interruptions and Voltage Variations Immunity Tests
[12/I07g] IEC 61000-4-11 (2004)
Voltage Dips, Short Interruptions and Voltage Variations Immunity Tests
[Z500013-I1] Exclusions
EN 61000-4-3 and ISO 61000-4-3 testing for tabletop equipment only
[Z500013-I2] Exclusions
ISO 61000-4-5 and EN 61000-4-5 testing excludes clause 6.2
[Z500013-I3] Exclusions
ISO 61000-4-8 and EN 61000-4-8 testing excludes "short duration" mode.
[12/A20]
MIL-STD-461 Version F Method CE102
[12/D12]
MIL-STD-461 Version F Method RE103
[12/21647] ISO/EN 21647 (2009), Clause 36
Medical electrical equipment. Particular requirements for the basic safety and essential performance of respiratory gas monitors
[12/60601h1] EN 60601-1-2 (2007)
Medical electrical equipment - Part 1-2: General requirements for safety - Collateral standard: EMC - Requirements and tests
[12/60601i3] IEC 60601-2-4 ed3.0 (2010), Clause 202
Medical electrical equipment - Part 2-4: Particular requirements for the basic safety and essential performance of cardiac defibrillators
[12/60601i4] EN 60601-2-4 (2003), Clause 202
Medical electrical equipment. Particular requirements for safety. Particular requirements for the safety of cardiac defibrillators
[12/60601k1] EN 60601-2-25 (1996), Clause 36
Medical electrical equipment. Particular requirements for safety. Specification for electrocardiographs
[12/60601l1] EN 60601-2-27:2006
Medical electrical equipment - Part 2-27: Particular requirements for the safety, including essential performance, of electrocardiographic monitoring equipment
[12/60601l2] IEC 60601-2-27 ed3.0 (2011), Clause 202
Medical electrical equipment - Part 2-27: Particular requirements for the basic safety and essential performance of electrocardiographic monitoring equipment
[12/60601m] IEC 60601-2-30:1999, EN 60601-2-30:2000
Particular requirements for the safety including essential performance, of automatic cycling non-invasive blood pressure monitoring equipment
[12/60601o1] IEC 60601-2-34 ed3.0 (2011), Clause 202
Medical electrical equipment - Part 2-34: Particular requirements for the basic safety and essential performance of invasive blood pressure monitoring equipment
[12/60601q] IEC 60601-2-47:2006, EN 60601-2-47:2001
Particular requirements for the safety, including essential performance, of ambulatory electrocardiographic systems
[12/60601r] IEC 60601-2-49:2006, EN 60601-2-49:2001
Particular requirements for the safety of multifunction patient monitoring equipment
[12/60601r1] IEC 60601-2-49 ed2.0 (2011), Clause 202
Medical electrical equipment - Part 2-49: Particular requirements for the basic safety and essential performance of multifunction patient monitoring equipment
[12/80601a] IEC 80601-2-30 ed1.0 (2011), Clause 202
Medical electrical equipment - Part 2-30: Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers
[12/80601b] EN 80601-2-30 (2011), Clause 202
Medical electrical equipment. Particular requirements for the basic safety and essential performance of automated non-invasive sphygmomanometers
[12/80601c] ISO 80601-2-61 (2011), Clause 202
Medical electrical equipment - Part 2-61: Particular requirements for basic safety and essential performance of pulse oximeter equipment
[12/ISO9919] ISO 9919 ed2.0 (2005), Clause 36
Medical electrical equipment - Particular requirements for the basic safety and essential performance of pulse oximeter equipment for medical use
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