Yes, China's National Medical Products Administration (NMPA) may accept CE marking approval as a reference for the registration of medical devices and diagnostics in China, but it is not guaranteed. The acceptance of CE marking as a reference depends on several factors, including the classification of the device, its intended use, and the specific requirements of the NMPA.
In some cases, having CE marking approval may streamline the registration process in China, as it demonstrates compliance with certain international standards and requirements. However, the NMPA may still require additional testing, documentation, or other requirements before granting registration in China.
It is advisable to consult with regulatory experts familiar with the NMPA regulations and requirements to determine the specific implications of CE marking approval for the registration of medical devices and diagnostics in China.