Good news! Focusfreda has successfully completed the filing of the main document for sodium hyaluronate raw materials for three types of medical devices!
Recently, the official website of the Medical Device Technical Evaluation Center of the National Medical Products Administration announced that the sodium hyaluronate raw material for three types of medical devices developed byFocusfreda has successfully completed the main document registration (main document registration number: M2025008-000), This achievement marks a milestone breakthrough for Focusfreda in the field of sodium hyaluronate raw materials for three types of medical devices.
Sodium hyaluronate, as a key component naturally present in human tissues, has played a wide range of application values in the three categories of medical devices, especially in the following aspects: it is widely used in the preparation of water light needle products to enhance skin moisture and radiance; As the core component of cross-linked sodium hyaluronate gel, it is used for filling and shaping; In the field of ophthalmology, as a viscoelastic agent, it effectively assists in ophthalmic surgical operations; In addition, it also serves as a key component of postoperative anti adhesion preparations, helping to reduce tissue adhesion after surgery.
The successful completion of the main document registration for sodium hyaluronate raw materials used in three types of medical devices is an important step taken by Focusfreda in the field of pharmaceutical grade sodium hyaluronate. In the future, Focusfreda will continue to deepen its research and development investment, continuously improve product quality and technological innovation capabilities, and strive to provide consumers with more high-quality pharmaceutical grade sodium hyaluronate products.
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