Legal analysis: purpose: for emergency, critical and serious patients, do not shirk, do not refuse to accept, adhere to the principle of life first, based on scientific evidence, adequate prevention and control of protection, open a green channel, priority rescue life.
(A) for emergency patients and can not be excluded when the new coronavirus infection, in accordance with the reception of suspected patients to do a good job of protection, first rescue treatment.
(2) new patients, single room admission, fixed escort, in the emergency isolation area / transition (buffer) ward to rule out the possibility of new coronavirus pneumonia before being transferred to the general ward for further hospitalization, to reduce the risk of potential cross-infection in the hospital.
(3) Emergency isolation area/transitional (buffer) ward set up contaminated area, potentially contaminated area and clean area, with clear zoning. The necessary protective equipment is provided (see annex for details).
(d) medical personnel before entering the contaminated area, in the clean area to wear protective gear; when leaving the contaminated area, through the buffer room to remove protective gear, and hand hygiene.
Legal basis: "Medical Device Supervision and Administration Regulations"
Article 1 In order to ensure the safety and effectiveness of medical devices, to protect human health and safety of life, the formulation of these regulations.
The second in the Chinese people *** and the State engaged in the development, production, operation and use of medical devices and their supervision and management activities, shall comply with these regulations.
Article 3 The Food and Drug Administration under the State Council is responsible for the supervision and management of medical devices throughout the country. The relevant departments of the State Council shall be responsible for the supervision and management of medical devices within their respective areas of responsibility.
The food and drug administration department of the local people's government at or above the county level is responsible for the supervision and management of medical devices in the administrative region. The relevant departments of the local people's government at or above the county level are responsible for the supervision and management of medical devices within their respective areas of responsibility.