EMC China Lab

What is Medical Device EMC Testing?

Views :
Update time : 2024-12-29

emc testing, also known as Electromagnetic Compatibility (EMC) testing, refers to the comprehensive evaluation of a medical device's electromagnetic interference (EMI) and electromagnetic susceptibility (EMS). It is one of the most critical indicators of product quality.

 

What is Medical Device EMC Testing?(图1)


Purpose of Medical Device emc testing 

1. Evaluate Electromagnetic Radiation: Assess the electromagnetic radiation emitted by medical devices to determine its impact on humans, public power grids, and other electrical equipment operating normally. 

2. Enhance Safety and Effectiveness: Improve the safety and effectiveness of medical devices by preventing potential hazards to patients and users due to electromagnetic interference or emissions causing device malfunction or failure.

 

EMC Standards for Medical Devices/In Vitro Diagnostics 

Domestic Standards: 

- GB 9706.102 

- GB/T 18268.1 

- GB/T 18268.26 

 

International Standards: 

- iec 60601-1-2 

- IEC/EN 61326-1 

- IEC/EN 61326-2-6 

 

EMC Testing Items for Medical Devices/In Vitro Diagnostics 

EMI (Electromagnetic Interference) Testing 

- Radiated Emission: Testing radiated electromagnetic disturbances. 

- Conducted Emission: Testing conducted electromagnetic disturbances. 

- Harmonic: Testing harmonic current disturbances. 

- Flicker: Testing voltage fluctuations and flicker disturbances. 

 

EMS (Electromagnetic Susceptibility) Testing 

- ESD: Electrostatic Discharge Immunity Testing. 

- RS: Radiated RF Electromagnetic Field Immunity Testing. 

- CS: Conducted RF Disturbances Immunity Testing. 

- DIP: Voltage Dips, Short Interruptions, and Voltage Variations Immunity Testing. 

- SURGE: Surge (Impact) Immunity Testing. 

- EFT: Electrical Fast Transient/Burst Immunity Testing. 

- PMS: Power Frequency Magnetic Field Immunity Testing. 

 

Common Sample Requirements 

- FULly functional and operational samples are requiRED for testing. For specific details, consult JJR online customer service.

 

Our Advantages 

1. Expert Team: JJR's team of experienced technical experts offers professional consultation and services. 

2. Advanced Equipment: State-of-the-art laboratory equipment ensures accurate and reliable testing data. 

3. Global Trust: JJR is a trusted third-party testing and certification institution globally, serving as a guarantee of quality. 

4. Comprehensive Solutions: Through a global network of laboratories, JJR provides end-to-end testing and certification solutions.

 

Frequently Asked Questions 

What is the testing timeline for JJR's medical device testing

The actual timeline depends on the product standards under commission. Please contact JJR customer service for confirmation. 

 

What are the testing methods used by JJR for medical devices? 

Testing methods are tailored to the product's export requirements and client-specific commissioning standards. 

 

What is the sample retention period for JJR? 

JJR supports sample returns upon request.

 

About JJR Laboratories 

JJR Laboratories, built to international leading and domestic first-class standards, feature advanced and fully functional electromagnetic compatibility labs. Our team specializes in EMC technology research and application, providing EMC services to industries such as automotive, aviation, rail transit, maritime, communications, and power sectors.


Email:hello@jjrlab.com


Leave Your Message


Write your message here and send it to us


Related News
Read More >>
What is a UK Authorized Representative? What is a UK Authorized Representative?
11 .22.2025
A UK Authorized Representative (UKRP) helps non-UK manufacturers meet UKCA rules, register products,...
Food Contact Materials LFGB Compliance Food Contact Materials LFGB Compliance
11 .22.2025
JJR Lab tests Food Contact Materials (FCM) for LFGB compliance, ensuring safety via EU/China standar...
Compliance Test Reports for Export to the US Compliance Test Reports for Export to the US
11 .22.2025
JJR guides US export compliance: CPC, FCC, UL/CSA/ETL, FDA tests ensure toys, electronics, appliance...
UKCA Certification to Replace CE Compliance in 202 UKCA Certification to Replace CE Compliance in 202
11 .22.2025
From 2028 UKCA replaces CE in Great Britain; firms must meet UK standards, ensure proper marking, an...
Does Your Product Need an FCC ID? Does Your Product Need an FCC ID?
11 .21.2025
FCC ID is required for all RF-transmitting devices; non-RF products use SDoC. Tests include RF &...
What Are the Battery Compliance Test Reports? What Are the Battery Compliance Test Reports?
11 .20.2025
Battery compliance needs safety, CE, UN38.3, air, drop tests to match labels; use IEC/UL standards; ...
Christmas Children’s Products EU & US Complian Christmas Children’s Products EU & US Complian
11 .20.2025
Prep for Christmas sales with compliant kids’ goods using US ASTM F963/CPSIA and EU EN71 tests; JJR ...
Food Packaging Material Testing Food Packaging Material Testing
11 .19.2025
China JJR Lab provides EU PPW & US TPCH food packaging testing (per 94/62/EC, 2004/12/EC) for Pb...

Leave Your Message