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Current Location:Home > Service Project > Medical Devices > Ⅲ Medical device business license
Ⅲ Medical device business license
Legal overview

According to the Regulations on the Supervision and Administration of Medical Devices and the Measures for the Supervision and Administration of Medical Devices Management, enterprises engaged in the management of Class III medical devices shall apply for a license to the municipal drug regulatory department where the district is located and obtain a business license.

Those engaged in medical device trading activities without filing or licensing will be confiscated of illegal income, illegal medical devices and tools, equipment, raw materials and other articles used for illegal production and business; If the value of the illegally traded medical devices is less than 10,000 yuan, a fine of not less than 50,000 yuan but not more than 100,000 yuan shall be imposed; If the value of the goods is not less than 10,000 yuan, a fine of not less than 10 times but not more than 20 times the value of the goods shall be imposed; If the circumstances are serious, the application for medical device license submitted by the relevant responsible person and enterprise shall not be accepted within 5 years.

 
Information to be provided

1. Copy of business license

2, legal representative, responsible person, quality responsible person identity, education, title certificate copy

3. Organization chart

4. Geographical location map, floor plan, proof of property rights or lease agreement of premises and warehouse (with proof of property rights)

5, computer information management system basic introduction and function description

6, operating equipment list

Remarks: As a municipal administrative business, the requirements vary from place to place, and the details are subject to the regional municipal requirements.

 
Filing period

Expected period of Class III business license: 1-3 months

The services we provide
  • Assembly license application complete set of materials (except system and field service)
  • System construction counseling and system and site pre-audit special consulting services
  • Full service from site planning to system and permit application
About Us
COC REACH LIMITED specializes in product registration and compliance consulting services. Leveraging its professional expertise, diverse resources, and global network, it is committed to providing regulatory consulting and environmental compliance services to pharmaceutical and chemical companies, consumer goods manufacturers, and large multinational corporations. It addresses issues related to environmental health and safety laws, product quality standards, and other challenges faced by enterprises during production, sales, and global trade processes.
Accumulated Customers
18,000+
Distributed in 35 countries and regions
15year
Industry experience
260+
Senior expert team
15+
Subsidiaries
300+
Collaboration Cases
  • Ireland Dublin
  • USA Denver
  • Korea Seoul
  • UK London
  • Qingdao
  • Beijing
  • Shanghai
  • Shenzhen
Contact Us
If you have any issues related to environmental health and safety laws and regulations, product quality standards, etc. that need to be resolved in import and export trade, you can contact us for assistance.
400-115-9001
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