NMPA Announces Cancellation of Registration Certificates for Nine Medical Devices Including Embryo Incubators

(Source: China Food and Drug Administration Network)

On March 10, the website of the National Medical Products Administration released the "Announcement on the Cancellation of Registration Certificates for 9 Medical Devices Including Embryo Culture Incubators," with the full text as follows.

NMPA Announcement on the Cancellation of Registration Certificates for 9 Medical Devices Including Embryo Culture Incubators

(No. 23, 2026)

According to the relevant provisions of the Regulations on the Supervision and Administration of Medical Devices, based on the enterprise's application, the National Medical Products Administration has canceled the medical device registration certificates for a total of 9 products from the following 4 enterprises:

1. One product of Planer Limited (Pu Lan Na Medical Device Co., Ltd.): Incubators, Registration Certificate No.: China Medical Device Registration No. 20222180361.

2. Four products of TRAUSON Medical Appliance (jiangsu) Co., Ltd.: Spinal Universal Posterior Fixation System, Registration Certificate No.: China Medical Device Registration Approval 20173134720; Spinal Universal Anterior Fixation System, China Medical Device Registration Approval 20183131572; Spinal Universal Posterior Fixation System, Registration Certificate No.: China Medical Device Registration Approval 20153130118; Interbody Fusion Cage, Registration Certificate No.: China Medical Device Registration Approval 20173131463.

3. Three products of Jiangsu Shuangyang Medical Instrument Co., Ltd.: Titanium Bone Plates (Compression and Protective Bone Plates), Registration Certificate No.: China Medical Device Registration Approval 20163130368; Titanium Bone Plates (Anatomical Bone Plates), Registration Certificate No.: China Medical Device Registration Approval 20163130451; Titanium Bone Plates (DHS, DCS), Registration Certificate No.: China Medical Device Registration Approval 20163130369.

IV. GuangdongBiolightOne product of Guangdong Biolight Meditech Co., Ltd.: Hemodialyzer, Registration Certificate No.: Z20223100152.

Hereby announced.

National Medical Products Administration

March 9, 2026

《China MedicineCopyright by the Press, no reprinting or use without permission.

(Editor: Chang Jingjie)