

According to the Regulations on the Supervision and Administration of Medical Devices, based on the enterprise's application, the National Medical Products Administration hereby cancels the medical device registration certificates for a total of 8 products from the following 5 enterprises:
1. Two products of AMO (Hangzhou) Pharmaceutical Co., Ltd.: Multi-purpose Contact Lens Solution, Registration Certificate No.: China Medical Device Registration 20163160810; Hydrogen Peroxide Contact Lens Disinfectant, Registration Certificate No.: China Medical Device Registration 20143161869.
2. Two products from AMO Ireland: Protein Remover Tablets for Contact Lenses, Registration Certificate No.: China Medical Device Registration No. 20163162781; Neutralizing Tablets for Hydrogen Peroxide Contact Lens Disinfectant Solution, Registration Certificate No.: China Medical Device Registration No. 20153163958.
3. One product of Smith&Nephew Surgical Implants (Beijing) Co., Ltd.: Non-cemented acetabular system, Registration Certificate No.: G20203130288.
4. Two products of JPI Healthcare.Co.Ltd (Korea Dingyuan Medical Co., Ltd.): Anti-scatter Grid for Mammography, Registration Certificate No.: Instrument Registration No. 20182060477; Anti-scatter Grid, Registration Certificate No.: Instrument Registration No. 20172067219.
5. One product of Nanjing Suyuan Gene Technology Co., Ltd.: Real-time Fluorescence Quantitative PCR Analyzer, Registration Certificate No.: G20233221332.
Hereby announced.
National Medical Products Administration
March 13, 2025
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