EMC China Lab

What is electromagnetic field conducted interference testing

Views :
Update time : 2025-11-10

emc testing, also known as Electromagnetic Compatibility (EMC), refers to a comprehensive evaluation of electronic products concerning the amount of interference in the electromagnetic field (EMI) and their ability to resist interference (EMS). It is one of the most critical indicators of product quality. The measurement of electromagnetic compatibility consists of test sites and test instruments.

 

The purpose of emc testing is to detect the impact of electromagnetic radiation generated by electrical products on humans, public power grids, and other electrical products operating normally.

 

Electromagnetic compatibility is a discipline that studies the coexistence of various electrical devices (broadly including organisms) in limited space, time, and spectrum resources without causing degradation. It includes two parts: electromagnetic interference and electromagnetic susceptibility. electromagnetic interference testing measures the strength of interference on surrounding electronic devices by detecting the size of the electromagnetic waves emitted by the tested equipment in normal working conditions. Electromagnetic susceptibility testing measures the ability of the tested equipment to resist electromagnetic interference.

 

Electromagnetic interference mainly includes radiated emissions and conducted emissions.

 

Radiated Emission:

Electromagnetic interference transmitted through space in the form of electromagnetic waves.

 

Conducted Emission:

Electromagnetic interference propagated along conductors.

 

Test Sites:

- Open-area test sites

- Semi-anechoic chambers

- Shielded rooms

 

Main Electromagnetic Interference testing Equipment:

1. Anechoic chamber

2. Receiver

3. Receiving antenna

4. Artificial power network

5. Power absorption clamp

6. Turntable and lift platform

7. Turntable and lift platform controller

 

Electromagnetic Compatibility Testing Items:

- Conducted emission (9kHz-30MHz)

- Power clamp emission (30MHz-300MHz)

- Magnetic emission (9kHz-30MHz)

- Radiated emission (30MHz-18GHz)

- Click conduction interference

- Harmonics (class A, B, C, D)

- Voltage flicker (flicker plt, pst)

- Electrostatic discharge (ESD ±0.1-±16.5kV)

- Radiated immunity (below 1GHz)

- Electrical fast transient/burst (EFT/B ±0.1-±4.4kV)

- Surge (0.1-6.6kV)

- Conducted susceptibility (CS 0.1-30V)

- Magnetic field immunity (MS 0-120A/m)

- Voltage dips (0%-100%)

- Oscillatory waves surge (0.1-6.6kV, 100kHz waveform)

- Harmonic and interharmonic immunity

- Magnetic field EFM 10Hz-400kHz (EN50366)


Email:hello@jjrlab.com


Leave Your Message


Write your message here and send it to us


Related News
Read More >>
2026 U.S. CPSC Mandates eFiling 2026 U.S. CPSC Mandates eFiling
04 .17.2026
From July 8, 2026, CPSC requires eFiling of Certificates for U.S. imports. JJR LAB helps exporters c...
U.S. CPSC Consumer Products Electronic Filing & U.S. CPSC Consumer Products Electronic Filing &
04 .17.2026
CPSC eFiling expands mandatory digital compliance for imports, strengthening product safety oversigh...
Does ce mark mean ROHS Compliance Does ce mark mean ROHS Compliance
04 .17.2026
CE mark ≠ RoHS compliance; RoHS is part of CE for electronics; CE covers broader safety rules. JJR p...
How to Become RoHS Compliant How to Become RoHS Compliant
04 .17.2026
How to become RoHS compliant: EU restricts 10 hazardous substances in EEE; companies must manage sup...
Shower Head DOE Registration Testing Fee Shower Head DOE Registration Testing Fee
04 .17.2026
China JJR Lab charges $688 for DOE registration testing of showerheads. Clients must provide 2 sampl...
Biological Evaluation of Medical Devices ISO 10993 Biological Evaluation of Medical Devices ISO 10993
04 .16.2026
JJR LAB performs ISO 10993 biological evaluations to ensure medical devices are safe for human use, ...
In Vitro Cytotoxicity Test for Biomedical Devices In Vitro Cytotoxicity Test for Biomedical Devices
04 .16.2026
JJR LAB conducts ISO 10993-5 in vitro cytotoxicity tests to ensure medical device safety, assessing ...
EU Responsible Person on Amazon EU Responsible Person on Amazon
04 .16.2026
EU Responsible Person is EU rep for non-EEA manufacturers ensuring compliance and regulatory require...

Leave Your Message