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Delivery: <= 4 days. True-PDF full-copy in English will be manually translated and delivered via email. YY/T 1643-2018: Functional and compatibility test methods for remote medical imaging equipment Status: Valid
Basic dataStandard ID: YY/T 1643-2018 (YY/T1643-2018)Description (Translated English): Functional and compatibility test methods for remote medical imaging equipment Sector / Industry: Medical Device & Pharmaceutical Industry Standard (Recommended) Classification of Chinese Standard: C30 Classification of International Standard: 11.040 Word Count Estimation: 19,163 Date of Issue: 2018-12-20 Date of Implementation: 2020-01-01 Quoted Standard: DICOM PS3.2; DICOM PS3.4 Regulation (derived from): State Drug Administration Announcement No. 97 of 2018 Issuing agency(ies): State Drug Administration Summary: This standard specifies the basic functions, image compatibility and interoperability testing methods for remote medical imaging equipment conforming to the DICOM 3.0 standard. YY/T 1643-2018: Functional and compatibility test methods for remote medical imaging equipment---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.(Functionality and compatibility test method for remote medical imaging equipment) ICS 11.040 C30 People's Republic of China Pharmaceutical Industry Standard Functionality and compatibility of remote medical imaging equipment Testing method Published on.2018-12-20 2020-01-01 implementation State Drug Administration issued ContentForeword III 1 Scope 1 2 Normative references 1 3 Terms and Definitions 1 4 Test conditions 1 5 Basic function test method 1 6 DICOM file format compatibility test method 6 7 Interconnection test method 6 Appendix A (Normative) Requirements for DICOM Compliance Test Tools required for Interoperability Testing 15 Appendix B (informative) Interpretation of abbreviations and abbreviations 16ForewordThis standard was drafted in accordance with the rules given in GB/T 1.1-2009. Please note that some of the contents of this document may involve patents. The issuing organization of this document is not responsible for identifying these patents. This standard was proposed by the State Drug Administration. This standard is under the jurisdiction of the National Medical Electrical Equipment Standardization Technical Committee (SAC/TC10). This standard was drafted. Shanghai Medical Device Testing Institute, Shanghai Lianying Medical Technology Co., Ltd., Shanghai Siemens Medical Devices Co., Ltd. the company. The main drafters of this standard. He Jun, Wang Shumei, Cao Jingtai, Liu Ruifei, Li Yong. Functionality and compatibility of remote medical imaging equipment Testing method1 ScopeThis standard specifies the basic functions, image compatibility and interconnection of remote medical imaging equipment conforming to the DICOM3.0 standard. Sex test method. Note 1. This standard is the test method standard. It does not require any function. The equipment manufacturer can use some or all of the items listed in this standard as needed. Testing method.2 Normative referencesThe following documents are indispensable for the application of this document. For dated references, only the dated version applies to this article. Pieces. For undated references, the latest edition (including all amendments) applies to this document. DICOMPS3.2 Medical Digital Imaging and Communications (DICOM) Part 2. Declaration of Conformity (Digitalimagingand Communicationsinmedicine(DICOM)-Part 2.conformance) DICOMPS3.4 Medical Digital Imaging and Communications (DICOM) Part 4. Service Class Specification (Digitalimagingand Communicationsinmedicine(DICOM)-Part 4.serviceclassspecifications)3 Terms and definitionsThe following terms and definitions apply to this document. 3.1 Remote medical imaging equipment remotemedicalimagingequipment A medical imaging device with information and data transmission function that complies with the DICOM 3.0 standard. 3.2 Patient management patientmanagement Used to manage and display patient information stored in the system for patient data management.4 test conditionsTo meet Chapters 6 and 7 testing, device manufacturers are required to provide a DICOM Declaration of Conformity document. DICOM Declaration of Conformity Please refer to DICOMPS3.2 for the specific requirements of the document.5 basic function test method5.1 Patient Management 5.1.1 Case Query Test Case Test purpose. to detect whether the user can obtain the expected case by query. ......Tips & Frequently Asked Questions:Question 1: How long will the true-PDF of YY/T 1643-2018_English be delivered?Answer: Upon your order, we will start to translate YY/T 1643-2018_English as soon as possible, and keep you informed of the progress. The lead time is typically 2 ~ 4 working days. The lengthier the document the longer the lead time.Question 2: Can I share the purchased PDF of YY/T 1643-2018_English with my colleagues?Answer: Yes. The purchased PDF of YY/T 1643-2018_English will be deemed to be sold to your employer/organization who actually pays for it, including your colleagues and your employer's intranet.Question 3: Does the price include tax/VAT?Answer: Yes. 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