EMC China Lab

Taiwan BSMI Certification for Electronic Products

Views :
Update time : 2024-11-11

bsmi stands for "Bureau of Standards, Metrology and Inspection," under the Ministry of Economic Affairs in Taiwan. According to an announcement from the Ministry of Economic Affairs in Taiwan, starting from July 1, 2005, products entering the Taiwan region are subject to supervision in terms of electromagnetic compatibility and safety.

Taiwan BSMI Certification for Electronic Products(图1)

Methods of Applying for bsmi certification: Currently, there are three application methods:

1. Type Approval, which includes two types:

   a. Type Approval (EMC + Safety): There are 178 types of electronic and electrical products requiring approval.

      Standards: EMC + Safety. Required documents include application for product type approval, company or factory license, test reports, EMC technical documents: photos, labels, EMC components, diagrams and user manuals, and technical documents for safety requirements. Certification validity: Three years, with one extension possible.

   b. EMC Type Approval

      Applicable products: 61 types of electronic and electrical products with only EMI requirements, and 124 types of electronic and electrical products requiring only EMI + safety reports (if safety standards are applicable). Applicable standard: EMI only. Required documents include EMC type approval application, test reports, technical documents: photos, labels, electromagnetic compatibility components, diagrams, and user manuals.

 

2. Certification Registration.

   Standards: EMI + Safety. Required documents include application for product type approval, company or factory license, test reports, electromagnetic compatibility technical documents: photos, labels, EMI components, diagrams and user manuals, safety technical documents, and a declaration of conformity. Certification validity: Three years, with one extension possible.

 

3. Declaration of Conformity.

   Product scope: 19 types of information technology equipment components. Standard in use: CNS13438 (ONLY EMC). Required documents include a declaration of conformity, test reports, technical documents: photos, labels, EMI components, diagrams, and user manuals. No certificate issued.

 

Documents Required for BSMI Certification:

The list of required documents for BSMI includes:

 

- Traditional Chinese version of the user manual

- Product specification sheet

- Labels

- List of important components (CDF)

- Circuit diagram

- Circuit copper trace diagram

- Applicant (holder) name:

- Applicant address:

- Applicant tax ID:

- Applicant representative:

- Contact person:

- Contact person's phone:

- Contact person's email:

- Manufacturer name:

- Manufacturer address:

- Product name:

- Brand:

- Model:


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