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    Medical Device Classification Rules

    I. China's Medical Device Classification Management System

    China implements classified management of medical devices according to the degree of risk.

    The Class I is the medical device that is low-risk and requires routine management to ensure its safety and effectiveness.

    The Class II is the medical device that is moderate-risk and requires strict control and management to ensure their safety and effectiveness.

    The Class III is the medical device that is high-risk and require special measures to strictly control management to ensure their safety and effectiveness.

    To evaluate the degree of risk of medical devices, factors such as the intended purpose, structural characteristics, and methods of use of medical devices should be considered.

    Classification

    Class I

    Class II

    Class III

    Registration Procedure

    Put on record

    Registration

    Registration

    Production Procedure

    Put on record

    Production Permit

    Production Permit

    Business Procedure

    N/A

    Put on record

    Business Permit

    II. Regulatory Documents Related to Medical Device Classification

    1. Medical Device Classification Rules (CFDA No. 15)

    2. Medical Device Classification Catalogue

    3. New edition of the Medical Device Classification Catalogue (No. 104 of 2017)

    III. Overview of the Latest Edition of the Medical Device Classification Catalogue 

     

    Version 2002

    New Version

    Sub-catalogue

    43

    22

    Product Category

    First-level subdirectory

     

    260

    206

    Second-level subdirectory

    1157

    Referenced Products

    1008

    6609

     

    Settings of Subdirectory

    Distribution of Subdirectory

    Surgical Medical Device

    01. Active surgical device

    02. Passive surgical device

    03. Neurosurgical and cardiovascular surgical device

    04. Orthopedic surgical device

    Active Medical Device

    05. Radiotherapy device

    06. Medical imaging device

    07. Medical examination and monitoring device

    08. Breathing, anesthesia and first-aid devices

    09. Physiotherapy device

    10. Blood transfusion, dialysis and extracorporeal circulation device

    11. Sterilizing device for medical devices

    12. Active implant device

    Passive Medical Device

    13. Passive implant device

    14. Injection, infusion, nursing and protective device

    15. Device to carry patients

    According to clinical departments

    16. Ophthalmic device

    17. Stomatological device

    18. Gynecological, assisted reproductive, and contraceptive devices

    Others

    19. Medical rehabilitation device

    20. Device for traditional Chinese medicine

    21. Medical software

    22. clinical examination device

    Note: IVD reagents and combination kits are not included in the new catalogue

     

    If you are unsure of the classification of your product, you could apply for a medical device classification.

      

    We have launched a LinkedIn newsletter to keep you up to date on the latest developments across the chemical industry including food and FCMs and personal and home care.

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