EMC China Lab

What is the Middle East DAB Certification?

Views :
Update time : 2025-03-12

DAB, or Digital Audio Broadcasting, is an advanced digital broadcasting technology that offers higher sound quality, a wider selection of channels, and additional services compared to traditional FM/AM broadcasting, making every listening experience an auditory feast.

 

In recent years, the demand for automobiles and components in the Middle East market has been increasing. With the introduction of DAB+ technology, in-car wireless certification has become essential. Therefore, for automotive manufacturers and component suppliers looking to enter or expand their market share in the Middle East, understanding and complying with relevant regulations is crucial.

 

Mandatory DAB+ Regulatory Requirements for Components (Based on MY2025)

The Gulf countries have imposed mandatory regulations on DAB+ components (such as external boxes, embedded head units, etc.):

 

1.United Arab Emirates (UAE): UAE.S 5021:2018

2.Saudi Arabia: SASO 2938:2019

3.GCC Gulf Five Countries (Bahrain, Kuwait, Oman, Yemen, Qatar) follow the Middle East Standard: GSO 2693:2022

 

DAB+ Certification Application Process & Timeline

1. Sample Submission

Test samples must include components such as head units, DAB boxes, screens, speakers, and radio antennas.

 

2. Certification Process

1. Submit TDRA registration application for the manufacturer or importer.

2. Get approval for the TDRA account for the manufacturer or importer.

3. Conduct product testing in a CNAS-accredited laboratory.

4. JJR Lab in China reviews the test report and submits the TDRA certification application.

5. TDRA reviews the submitted documents and test reports.

6. Obtain the TDRA product certificate.

 

3. One-Stop DAB+ Solution by JJR Lab in China

 

4. Certification Timeline

- Testing & Report Issuance: 2-3 weeks (for smooth testing)

- Certificate Application: 3-4 weeks

 

Testing Requirements

- General DAB functionality requirements

- RF (Radio Frequency) requirements

- DAB+ channel decoding & audio decoding requirements

- Functional and user interface requirements

- Announcement signaling, switching, and service labeling

 

Middle East Regulatory Requirements for Smart In-Car Components (RF Certification)

For DAB+ integrated components such as DAB boxes, external boxes, and embedded head units to gain recognition in GCC countries, manufacturers must obtain both:

 

1. DAB Certification (Test Report/Certificate)

2. RF Wireless Certification

 

Before applying for certification in individual countries, the product must first pass CE RED Certification.


Email:hello@jjrlab.com


Leave Your Message


Write your message here and send it to us


Related News
Read More >>
Toothbrush FDA Certification Testing Toothbrush FDA Certification Testing
04 .17.2025
FDA certification for toothbrushes ensures safety and compliance. JJR Laboratory in China offers tes...
Snoring Device FDA 510k Standard Testing Snoring Device FDA 510k Standard Testing
04 .17.2025
JJR Lab in China offers FDA 510(k) testing for snoring devices, including ISO 10993 biocompatibility...
Single Use Intravenous Catheter Certification Test Single Use Intravenous Catheter Certification Test
04 .17.2025
China JJR Laboratory offers testing for Single-Use Intravenous Catheters, including biocompatibility...
Silicone Material Product Compliance Certification Silicone Material Product Compliance Certification
04 .17.2025
Silicone products require various certifications (RoHS, REACH, FDA, LFGB, NSF, ISO 10993, USP, UL) b...
What to Do If Cytotoxicity Test Results Are Positi What to Do If Cytotoxicity Test Results Are Positi
04 .17.2025
If cytotoxicity test results are positive, further investigation is needed. JJR Lab provides testing...
ISO 10993:5 Cytotoxicity Testing Methods ISO 10993:5 Cytotoxicity Testing Methods
04 .17.2025
Cytotoxicity testing methods include MTT, agar, membrane, and direct contact methods per ISO 10993-5...
FDA ISO 10993-1 Biocompatibility Evaluation Guidel FDA ISO 10993-1 Biocompatibility Evaluation Guidel
04 .17.2025
FDA and ISO 10993-1 guidelines outline biocompatibility evaluation for medical devices. JJR Laborato...
In Vitro Cytotoxicity Testing for Medical Devices In Vitro Cytotoxicity Testing for Medical Devices
04 .17.2025
JJR LAB provides in vitro cytotoxicity testing for medical devices, helping assess material safety, ...

Leave Your Message