The National Medical Products Administration announces the cancellation of the registration certificates for 12 medical devices, including Spinal Internal Fixation Systems.

In accordance with the "Regulations on the Supervision and Administration of Medical Devices," and based on applications from enterprises, the National Medical Products Administration has now canceled the medical device registration certificates for a total of 12 products from the following 8 enterprises:

1. The product of Kelin Tai Co., Ltd.: Spinal Internal Fixation System, Registration Certificate Number: Guo Xie Zhu Jin 20173136765.

II. One product from Shanxi Yinuo Medical Technology Co., Ltd.: Single-use Negative Pressure Closed Drainage and Management System, Registration Certificate Number: National Medical Device Approval 20183140472.

III. One product from Johnson & Johnson Vision Care: Posterior Chamber PMMA Intraocular Lens, Registration Certificate Number: Guo Xie Zhu Jin 20163161337.

Four, Cheng Shin Hsin Ye Corporation Taoyuan Plant Company has 1 product registered: Dental Zirconia Ceramic Block, registration number: National Medical Device Registration 20232170021.

Five, Airon Medical Co., Ltd.'s three products: Gastrointestinal Nutritional Tube, registration number:国械注进20152141918; Gastric Stoma Length Gauge, registration number:国械注进20182141890; Radiofrequency Trocar, registration number:国械注进20223140375.

VI. One product from Xiamen Xinkangshun Medical Technology Co., Ltd.: Disposable Hydrophilic Coated Guide Wire, Registration Certificate No.: National Medical Device Approval 20223031532.

Seven, the two products of Spine Art Company: Cervical Anterior System, registration certificate number: National Medical Device Registration 20163132044; Lamina Fixator, registration certificate number: National Medical Device Registration 20163131692.

8. Two products from Xi'an Ouzhong Material Technology Co., Ltd.: Dental laser selective melting cobalt-chromium alloy powder, registration certificate number: National Medical Device Registration No. 20203170572; Dental laser selective melting titanium alloy powder, registration certificate number: National Medical Device Registration No. 20213170503.

Hereby announced.

National Medical Products Administration

March 27, 2025