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Portable CT BodyTom

As the world’s first portable, full-body, 32-slice CT (computed tomography) scanner, BodyTom® is a multi-departmental imaging solution capable of transforming any room in the hospital into an advanced imaging suite. The system boasts an impressive 85cm gantry and 60cm field of view, the largest field of view available in a portable CT scanner.

The battery-powered BodyTom with an innovative internal drive system can easily be transported from room to room and is compatible with PACS, EMR, planning systems, surgical and robotic navigation systems.

Uniquely designed to accommodate patients of all sizes, BodyTom provides point-of-care CT imaging wherever high-quality CT images are needed, including the operating room, intensive care unit, radiation oncology suites, and the emergency department. The combination of rapid scan time, flexible settings, and immediate image viewing makes the BodyTom a valuable tool to any facility needing versatile real-time portable imaging.

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F A Q

Is it legal for manufacturers to cope with issues of initial registration without an agent ?

Unfortunately, it is NOT legal unless the manufacturers have branches with qualification in China to deal with the registration issues. Otherwise, it is a must-do that manufacturers overseas are required to appoint a Chinese agent for the medical device registration.

In terms of the initial registration for market entry of mainland China, what is the registration fee needed ?

Regarding the registration fee for NMPA, as for the imported medical devices, the registration of Class II medical device needs 210,900 CNY while that of Class III costs 308,800 CNY. In addition, other kinds of possible fees should be taken into consideration such as fees of document translation, clinical trial, and so forth.

How long is the NMPA review process for the initial registration of the medical device ?

After the registration materials are accepted by NMPA, technical review for Class II medical devices takes 60 working days to process while for Class III medical devices, technical review takes 90 working days. If supplementary materials are required by NMPA, manufacturers are obliged to conduct submission within one year, otherwise the review may result in termination.

Is it possible for a medical device with CE or FDA certificate to enter SAR (HK/MO) and pilot area such as Hainan and the Greater Bay Area ?

MDs with CE or FDA certificate are feasible to enter SAR without NMPA certificate. As for the Greater Bay Area and Hainan province, MDs marketed in HK or MO as a premise can enter the pilot areas if designated medical institutions in pilot areas are willing to procure medical devices out of clinical urgent needs under the approval of local government.