National Medical Products Administration Approves Registration of 193 Medical Devices in February 2024
The National Medical Products Administration announced the approval of 193 medical devices in February 2024. Among these, there were 148 domestic Class III medical devices, 21 imported Class III devices, 22 imported Class II devices, and 2 medical devices from Hong Kong, Macau, and Taiwan. The approved devices cover a wide range of medical equipment necessary for healthcare facilities and professionals.
The imported Class III medical devices include advanced equipment such as the Dual-Wavelength Laser Therapy Device from Candela Corporation, X-ray Computer Tomography Imaging Equipment from GE Healthcare Japan, and Soft Corneal Contact Lenses from Johnson & Johnson Vision Care, Inc. These devices play crucial roles in various medical procedures and treatments.
Additionally, the list of imported Class II medical devices features essential tools like the D-Dimer Quality Control Product from Instrumentation Laboratory Company, the LED Curing Light Device from 3M Deutschland GmbH, and the Bladder Ultrasonic Scanner from Vitacon AS. These devices contribute to improving diagnostic accuracy and treatment outcomes in medical settings.
The approval of these medical devices signifies a significant step in enhancing healthcare services and ensuring access to cutting-edge medical technology in the country. The diverse range of approved devices reflects the continuous efforts to meet the evolving needs of the healthcare industry and provide patients with advanced treatment options.
For any inquiries or further information, please contact TX Medical at contact@txcro.com.