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Siemens and P+F Products + Features Gain NMPA Innovation Status


The NMPA granted innovative device status to seven devices, including two imported ones:

  • Siemens Healthcare: X-ray Computed Tomography Equipment
  • P+F Products + Features: Transcatheter Bicaval Valves System
  • United Imaging: Magnetic Resonance Imaging System
  • Yongxin Medical: Single Photon Emission and X-ray Computed Tomography System
  • Beijing Wanjie Tianyuan Medical: Artificial Ligament
  • Hangzhou Pulse Technology: Intracranial Aneurysm Interventional Surgery Planning Software
  • Tianjin Eagle Taili Ankang Medical Pulse Field Ablation Therapy Apparatus

Overseas Clinical Data

The overseas clinical trial data has been utilized by NMPA to evaluate imported devices’ clinical performance.

The latest example was Transcatheter Aortic Valve System from Edwards Lifesciences, whose Innovation Approval was granted by NMPA on June 8, 2020. Edwards Lifesciences provided overseas PIIS3HR cohort clinical trial data. The overseas data is supported by clinical trial data in China and literature review of the device and its similar predicates, which demonstrated that the genetic differences do not pose safety and efficacy issues.

We have the NMPA Evaluation Reports for 104 Innovation Devices and Priority Devices approved since November 2017. Please email us at for more information

Key Takeaways for Overseas Manufacturers

Only one out of five medical devices granted Innovative Device Status (not approved yet) by NMPA in 2019 were imported. Since domestic and overseas manufacturers have equal opportunity for this program, U.S. and European companies may not be taking full advantage.

Of the 39 innovation device status in 2019, only eight (just about 20%) were imported devices. One of those is Cardiovascular Systems, a company represented by China Med Device, LLC. China Med Device also conducted clinical trials for United Imaging’s CT-Linac, a combination of CT and accelerator for cancer radiotherapy. NMPA granted Innovation Approval to CT-Linac in December 2018. Email to see if you are qualified to apply.

Overseas manufacturers have to bear in mind that:

  1. The NMPA gives overseas manufacturers equal opportunity for the fast-track channels. No difference as to the qualifications for domestic manufacturers vs. overseas ones;
  2. “Conditional Approval” applies for urgently-needed medical devices. NMPA issue the “Guideline on Conditional Approval for Medical Devices” on December 20, 2019. It specifies that devices and IVDs indicated for life-threatening illnesses can be granted “Conditional Approval”, if the benefits of the products overweigh the risks, and the manufacturers are committed to do further clinical research;
  3. They can initiate innovation approval applications at same time when applying China Patent & Trade Office coverage. Application does not have to be made after getting the patent;
  4. Having been granted “status” does not mean “approval”. With ‘front-of-queue’ priority, they still have to go through the normal review process.

China Med Device has translated “Innovation Approval Procedure for Medical Devices” and other official NMPA documents into English as a service for its clients. Email for details.

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