Release date: 2014-07-01
The US Food and Drug Administration (FDA) announced on Thursday that it has officially approved the sale of the Rewalk bone mechanical suit of Argo, the Israeli bone mechanical wear manufacturer, in the United States, the first rehabilitation robot approved by the FDA.
The Rewalk mechanical suit helps the patient who is paralyzed by the cervical spine to stand and walk again by supporting the buttocks and knees. Argo found 30 participants in the clinical phase and conducted a comprehensive test of the company's Rewalk mechanical suits, including distance, speed, and different plane walks.
According to Christy Foreman of the FDA's Center for Medical Devices and Radiation Health, Rewalk products help patients with a certain degree of walking ability. After physical therapy, training and adaptation, these patients are expected to rely on Rewalk to walk autonomously.
According to the US Centers for Disease Control and Prevention, about 200,000 people have cervical spine injuries throughout the year, many of whom are paralyzed.
The company involved in the concept of medical robots in the A-share market mainly has GQY Video (300076.SZ). The company invested in the establishment of a wholly-owned subsidiary, Shanghai Yinhe Robot Co., Ltd., which is mainly engaged in research and development, production and sales of special service robots, including fire protection and medical services. Fields and industrial automation.
Source: Great Wisdom AASTOCKS News Agency
Preservation tubes are swabs with disposable virus sampling tubes to collect DNA tests for disposable nasal flocking sterile medical transport.
swabs with disposable virus sampling tubes , to collect DNA tests for disposable nasal flocking sterile medical transport.
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