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Standard ID | Contents [version] | USD | STEP2 | [PDF] delivered in | Standard Title (Description) | Status | PDF |
SN/T 4618-2016 | English | 229 |
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Rules of disinfection technique in medical screened room at the frontier
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SN/T 4618-2016
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Basic data Standard ID | SN/T 4618-2016 (SN/T4618-2016) | Description (Translated English) | Rules of disinfection technique in medical screened room at the frontier | Sector / Industry | Commodity Inspection Standard (Recommended) | Classification of Chinese Standard | C62 | Word Count Estimation | 10,153 | Date of Issue | 2016-08-23 | Date of Implementation | 2017-03-01 | Regulation (derived from) | State-Quality-Inspection-Certification (2016)438 | Issuing agency(ies) | General Administration of Customs |
SN/T 4618-2016: Rules of disinfection technique in medical screened room at the frontier---This is a DRAFT version for illustration, not a final translation. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.) will be manually/carefully translated upon your order.
Rules of disinfection technique in medical screened room at the frontier
China's entry-exit inspection and quarantine industry standards
Technical Specifications for Disinfection at Frontier Medical Examination Rooms
Published on.2016-08-23
2017-03-01 Implementation
China
The State Administration of Quality Supervision, Inspection and Quarantine issued
Foreword
This standard was drafted in accordance with the rules given in GB/T 1.1-2009.
This standard is proposed and managed by the National Certification and Accreditation Regulatory Commission.
This standard was drafted by. Guangdong Entry-Exit Inspection and Quarantine Bureau of the People's Republic of China and Xinjiang Entry-Exit Inspection and Inspection
Epidemic Bureau.
The main drafters of this standard are. Liao Ruyan, Bai Jing, Ge Cuiqi, Zhang Xianguang, Chen Hexiang, Lin Yanru, Chen Yuyu, Chen Guoqiu, Wu Hao, Huang Wei,
Dai Jun.
Technical Specifications for Disinfection at Frontier Medical Examination Rooms
1 Scope
This standard stipulates the disinfection requirements at the frontier medical check-up room, the implementation of disinfection, and the monitoring of the effects.
This standard is applicable to the disinfection of the port medical examination room of frontier inspection and quarantine agencies.
2 Normative references
The following documents are indispensable for the application of this document. For dated references, only dated versions apply to this article
Pieces. For undated references, the latest version (including all amendments) applies to this document.
WS/T 367 Medical Disinfection Technical Specifications
WS/T 1313 Hand Hygiene Specifications for Medical Staff
3 Terms and Definitions
The following terms and definitions apply to this document.
3.1
Port Medical Fighting Room frontierportmedicalinvestigationroom
Sites for medical investigation of suspected cases at ports include epidemiological investigations, isolation and observation, clinical specimen collection and rapid screening
Check the experiment and other areas.
3.2
High-risk items criticalitems
Into the body's sterile tissue, organs and blood flow, or contact with damaged skin, broken mucous membranes, once contaminated with microorganisms, has a very high
Risk of infection, such as puncture needles, blood collection needles, and used rapid screening test materials.
3.3
Moderately dangerous goods semi-critical items
Contact with intact mucous membranes without entering the body's sterile tissue, organs and bloodstream, and without touching damaged skin, damaged mucous membranes, etc.
Depressors, throat swabs, and anal swabs.
3.4
Low-risk items non-critical items
Contact with intact skin without contact with mucous membranes.
Note. Such as stethoscopes, sphygmomanometer cuffs, etc.; bed fences, bed and bedside cabinets, bedding; walls, floors; 痰盂 (cups) and toilets.
3.5
Disinfectant
Formulations that can kill pathogenic microorganisms on the media and achieve disinfection requirements.
3.6
Disinfection
Elimination or killing of pathogenic microorganisms on the media to make them harmless.
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