Can a Class II filing company commission storage and distribution of Class III products?

The second category of the company can not be entrusted with the storage and distribution of class III products. Class II filing is not allowed to engage in Class III medical device business, Class III can not engage in Class II sales business. Class II and Class III medical devices can be operated concurrently, both need to apply for relevant qualifications. The operation of Class II medical devices, do not need to apply for the "Medical Device Business License", only need to be filed with the relevant departments. Implementation of the record management, the operator must have a Class II medical device quality management system, qualified professional and technical personnel and the corresponding business premises. Class III is strictly managed and a license can only be obtained after applying for an examination. One license can operate three related businesses. According to the risk level of medical devices, the state implements classified management of medical devices. Class I medical devices do not require licensing and filing, Class II medical devices require filing, and Class III medical devices require licensing. Medical device business enterprises engaged in the second class of medical devices in the local municipal food and drug supervision and management department to obtain the medical device business filing certificate. The Medical Device Business License is obtained by applying for the Class III Medical Device Business Enterprise License from the local municipal food and drug supervision and management department. Enterprises can sell Class II medical devices within the approved scope after obtaining the Certificate of Registration of Medical Device Business Enterprise. Enterprises can sell Class III medical devices within the approved scope after obtaining the Medical Device Business License.