EMC China Lab

Introduction to METI Registration in Japan

Views :
Update time : 2024-09-25

The Ministry of Economy, Trade and Industry (METI) of Japan has released detailed information regarding this method, developed by the Commerce and Information Policy Bureau's Information Economy Division. The PSE product meti registration requires compliance with Japan's DENTORL law (Electrical Appliances and Materials Control Law), mandating that Japanese purchasers must register and declare their products to METI within one month of acquisition. Additionally, the purchaser's name or ID must be marked on the product for future sales monitoring. In other words, electronic products must be METI registeRED to be sold in Japan.

 

pse certification

1. PSE Certification: This is Japan's mandatory safety certification that verifies electrical and electronic products have passed safety standards testing under the DENAN Law or international IEC standards.

2. Under the DENTORL law, products entering the Japanese market must pass PSE safety certification. Among these, 116 types of Class A products require a diamond-shaped pse mark, while 341 types of Class B products need a circULar PSE mark.

3. All products within the PSE certification scope must be registered with METI by Japanese purchasers within one month of purchase to obtain approval documentation.

 

Registration Requirements

1. Notification of Business: This declaration by the Japanese importer includes manufacturer information, product details, and signing date.

2. Approval Documentation: The approval certificate issued by METI requires that the importer presents the PSE supplementary certificate to METI for registration.

3. Japanese purchasers must register with METI within one month of acquiring products, and only those with registered Japanese trading companies can apply for registration.

4. METI registration is divided into two types:

   1) With importer qualifications;

   2) Without importer qualifications (importer qualification can be leased).

 

Declaration Process

1. The applicant submits the application documents.

2. Testing reports and relevant documents are submitted to METI.

3. Application documents are registered.

4. Product label design and confirmation.

 

Documentation Checklist

1. Application form

2. PSE testing report (products with batteries or adapters also require their own PSE testing reports)

3. Product manual (in Japanese and English)

4. Product specification sheet (BOM, product photos)

5. Statement of differences (if there are series models in the report)


Email:hello@jjrlab.com


Leave Your Message


Write your message here and send it to us


Related News
Read More >>
Canada ISED Certification (IC Certification) Analy Canada ISED Certification (IC Certification) Analy
12 .20.2025
Canada ISED Certification: Mandatory EMI & wireless testing (ICES/RSS standards). JJR Lab provid...
CSA C22.2 No.42 Compliance Test Report for Amazon CSA C22.2 No.42 Compliance Test Report for Amazon
12 .20.2025
Amazon Canada requires USB plug-in products to meet CSA C22.2 No.42 safety rules. JJR Laboratory pro...
FCM Food Contact Materials Compliance Certificatio FCM Food Contact Materials Compliance Certificatio
12 .20.2025
FCM Food Contact Materials Compliance Testing verifies food-contact safety under EC 1935/2004 throug...
EN14350 Testing for Amazon Baby Feeding Products EN14350 Testing for Amazon Baby Feeding Products
12 .20.2025
Amazon baby feeding products must comply with EN 14350 and EU 10/2011 safety standards; JJR Laborato...
Infant Support Pillow 16 CFR 1243/1242 & ASTM Infant Support Pillow 16 CFR 1243/1242 & ASTM
12 .19.2025
Infant Support & Nursing Pillows must meet CPSC 2025 rules, including 16 CFR 1243/1242 & AST...
BRM Registration Card Under CFR Part 1130 Regulati BRM Registration Card Under CFR Part 1130 Regulati
12 .19.2025
Required for CFR Part 1130 infant products, the BRM Card supports CPC compliance and U.S. address ve...
How to get a D-U-N-S® Number for US FDA Registrati How to get a D-U-N-S® Number for US FDA Registrati
12 .18.2025
Get your D-U-N-S® Number for FDA registration. JJR LAB helps medical device firms apply fast, meet t...
Household Massage Devices Compliance in the China Household Massage Devices Compliance in the China
12 .18.2025
JJR LAB ensures household massage devices comply in China & Japan: CQC (GB4706.1/10), PSE (J/IEC...

Leave Your Message