Source: Qinhuangdao Release
Medical infrared thermometers has become an essential anti-epidemic material for enterprises and institutions when they are resuming work and production.
In order to fully support the production of medical devices during the epidemic prevention and control, on February 19, Hebei Drug Supervision Administration issued the Approval for Consent to Contec Medical System (Qinhuangdao) Co., Ltd. Emergency Production License for the Epidemic Prevention and Control Supplies, and Medical Device Registration Certificate to Contec Medical System (Qinhuangdao) Co., Ltd., so that it can produce medical infrared thermometers during the epidemic prevention and control, which indicates that Hebei Province will be able to mass produce and supply medical infrared thermometers, filling the gap of production of such products in Hebei.
At present, the company can produce 2,000 medical infrared thermometers per day, and is actively coordinating the supply of raw materials to further expand its production capacity.
In order to fully do a good job in the COVID-19 prevention and control, and effectively guarantee the supply of urgently needed medical equipment for the epidemic prevention and control, Hebei Drug Supervision Administration has included the medical protective masks, infrared temperature measurement equipment, supporting accessories for respiratory anesthesia equipment, medical oximeters, alcohol cotton sheets, disposable sterile rubber surgical gloves, disposable sterile medical rubber check gloves, digital mobile X-ray machines, the second-class medical device emergency approval product catalog, such as the second-class in vitro diagnostic reagents and instruments related to virus detection, which is based on the principle of handling special cases with special methods, launched the emergency approval process to speed up review and approval, and ensure that relevant medical devices are put into production as early as possible with measures, such as early involvment and full-service. The drug supervision authorities at all levels should strengthen the supervision and inspection on newly approved production enterprises and products, thus urge the enterprises to implement their principle responsibilities, produce according to laws and regulations, and firmly adhere to the quality and safety red line to ensure the quality, safety and effectiveness of the emergency medical devices.
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