To all relevant organizations and individuals:

In accordance with the relevant work requirements of the National Medical Products Administration and based on the "Dynamic Adjustment Procedures for the Medical Device Classification Catalog," the Medical Device Standardization Management Center of the National Medical Products Administration organized the Clinical Laboratory Professional Group of the Medical Device Classification Technical Committee to study and formulate the "Proposed Dynamic Adjustments to Certain Contents of the <In Vitro Diagnostic Reagents Classification Catalog>."), now open to the public for comments.