According to the principle, it stipulates that not only the large-scale Radio Frequency (RF) beauty equipment used by beauty institutions but also household RF beauty instruments are very likely to be included in the scope of medical device supervision.
In this case, massive RF beauty products that are currently sold in the China market could be necessary to do medical device compliance in the future.
Radio Frequency Beauty Products will be regulated as medical devices.
In accordance with the principles, RF beauty products that meet the following attributes will be managed as medical devices. Based on the level of product risk, the management category should not be lower than Class II. Specific attributes defining as follows:
According to the definition made by the principles above, CosmeticsBridge found that the currently best-selling home radio frequency beauty devices on the market are similar to the first type of RF products. The home RF beauty device mainly uses RF energy to directly act on the dermis to heat the collagen fibers and shrink the collagen fibers, so as to achieve the effect of lifting and tightening and improving fine lines. This means that the household Radio Frequency beauty devices will be definitely managed as medical devices.
High-end beauty Device business in China will Be Reshuffled.
The scale of China’s beauty devices market in 2019 was 6.62 billion RMB, with an output of 6.794 million units, a year-on-year increase of 21.82%, and it has become a major increasing market in the beauty field in recent years. Specific to the radio frequency beauty devices, it is a typical representative of the high-end beauty devices market, and the price is often more than 1,000 RMB. Most of the famous overseas beauty equipment brands almost all launched radio frequency beauty equipment in China. This year, the newly revised “Regulations on the Supervision and Administration of Medical Devices” also used the concepts of registrant and filing person as cosmetics to strengthen the main responsibility of enterprises, optimize the approval filing procedures, encourage innovation, and increase penalties for illegal acts. According to the regulation, Class I of medical devices with lower risk is required to do the notification/filing. But Class II and Class III types of medical devices are all necessary to do the registration and obtain a marketing permit before they can be put into the markets. And the registration will consume huge extra time and cost investment of the brands. As a result, if radio frequency beauty products are included in the management of medical devices, it will not only affect the home radio frequency beauty devices market, but may also set off a storm in the entire high-end beauty devices market.