If there are multiple models and accessories in the application registration unit of active medical devices, the administrative counterparts shall take all products (including all models and accessories) in the registration unit as delivered testing samples, and the EMC test report shall specify the information of delivered testing samples and tested samples.
If a typical sample is selected for testing after analysis or pretest, the administrative counterparts shall provide evidence and make a typical model description in the report, and the conclusion of the EMC test report shall clarify whether the sample meets the EMC requirements and standards.
