NMPA Announcement No. 28 of 2025 on Cancellation of Registration Certificates for Eight Medical Devices Including Multipurpose Contact Lens Care Solution

In accordance with 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 Approval 20163160810; Hydrogen Peroxide Contact Lens Disinfectant, Registration Certificate No.: China Medical Device Registration Approval 20143161869.

2. Two products of AMO Ireland: Protein Removers for Contact Lenses, Registration Certificate No.: China Medical Device Registration No. 20163162781; Neutralizing Tablets for Hydrogen Peroxide Contact Lens Disinfectant, 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): Anti-scatter Grid for Mammography, Registration Certificate No.: China Medical Device Registration No. 20182060477; Anti-scatter Grid, Registration Certificate No.: China Medical Device Registration No. 20172067219.

5. One product of Nanjing Suyuan Gene Technology Co., Ltd.: Real-time Fluorescence Quantitative PCR Analyzer, Registration Certificate No.: National Medical Device Registration Approval 20233221332.

Hereby announced.

Source: National Medical Products Administration

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