Hospital inspection identified three focus on molecular sieve oxygen

Health News (Reporter Wang Lemin) July 25, the State Food and Drug Administration held a national medical molecular sieve oxygen equipment special inspection group working conference in Beijing. The meeting identified the key elements of this inspection work. State Food and Drug Administration Medical Device Division Wangbao Ting said the focus of the inspection focused on three aspects: First, check the medical institutions for medical activated zeolite molecular sieve oxygen equipment have not registered a license, the second is to check the medical molecular sieve system maintenance of oxygen equipment, the use of compliance with relevant regulations and standards, is sampling and testing equipment produced three oxygen concentration is qualified. April this year, the State Food and Drug Administraactivated zeolite sieve oxygen equipment. After the meeting, six inspection teams to Beijing, Jiangsu, Zhejiang, Shandong and other 18 provinces (autonomous regions and municipalities) to carry out a 10-day inspection.

tion launched a medical institution medical molecular sieve oxygen equipment special inspection. Medical institutions around the self, food and drug regulatory departments of medical institutions were random. The previous phase of this inspection is intended to further promote special inspection work to further standardize and improve the safety level of protection of medical