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On March 3, the official website of NMPA showed that the application for the registration of innovative products of the "Mobile Head and Neck Magnetic Resonance Imaging System" produced by Foshan Ruijiatu Medical Technology Co.
, Ltd.
has been approved
.
The product consists of permanent magnet, gradient amplifier, gradient shim coil, RF amplifier, RF transmit coil, head coil (optional), head and neck combined coil (optional), spectrometer, temperature controller, digital shim unit, mobile It consists of a device, a shielding cover, a hospital bed, and an alarm unit for clinical MRI diagnosis of the head and neck
.
The product has the characteristics of movable, small size, light weight and integrated structure
.
It can be deployed inside a medical institution with a fixed shield outside, and can be used with an external 220V AC/10A network power supply; it can also be moved to different sites in the medical institution to conduct close examinations on patients, which expands the installation range of magnetic resonance products
.
The drug supervision and administration department will strengthen the post-market supervision of the product to protect the safety of patients using the device
.
, Ltd.
has been approved
.
The product consists of permanent magnet, gradient amplifier, gradient shim coil, RF amplifier, RF transmit coil, head coil (optional), head and neck combined coil (optional), spectrometer, temperature controller, digital shim unit, mobile It consists of a device, a shielding cover, a hospital bed, and an alarm unit for clinical MRI diagnosis of the head and neck
.
The product has the characteristics of movable, small size, light weight and integrated structure
.
It can be deployed inside a medical institution with a fixed shield outside, and can be used with an external 220V AC/10A network power supply; it can also be moved to different sites in the medical institution to conduct close examinations on patients, which expands the installation range of magnetic resonance products
.
The drug supervision and administration department will strengthen the post-market supervision of the product to protect the safety of patients using the device
.
