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MSZ EN ISO/IEEE 11073-10420:2023
Egészségügyi informatika. Az eszközök interoperabilitása. 10420. rész: Személyi egészségügyi eszközök kommunikációja. Eszközönkénti részletezés. Testösszetétel-analizátor (ISO/IEEE 11073-10420:2022)
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Health informatics. Device interoperability. Part 10420: Personal health device communication. Device specialization. Body composition analyzer (ISO/IEEE 11073-10420:2022)
Alkalmazási terület
1.1 Scope Within the context of the ISO/IEEE 11073 family of standards for device communication, this standard establishes a normative definition of the communication between personal body composition analyzer agents and managers (e.g., cell phones, personal computers, personal health appliances, set-top boxes) in a manner that enables plug-and-play interoperability. It leverages appropriate portions of existing standards including ISO/IEEE 11073 terminology, information models, application profile standards, and transport standards. It specifies the use of specific term codes, formats, and behaviors in telehealth environments to restrict optionality in base frameworks in favor of interoperability. This standard defines a common core of communication functionality for personal telehealth body composition analyzers. In this context, the phrase “body composition analyzer” is used broadly to cover analyzing devices that measure body impedances and compute the various body components including body fat from the impedance. 1.2 Purpose This standard addresses a need for an openly defined, independent standard for controlling information exchange to and from personal health devices and managers (e.g., cell phones, personal computers, personal health appliances, set-top boxes). Interoperability is key to growing the potential market for these devices and enabling people to be better informed participants in the management of their health. 1.3 Context See IEEE Std 11073-20601™ for an overview of the environment within which this standard is written.1 This standard defines the device specialization for the body composition analyzer, being a specific agent type, and it provides a description of the device concepts, its capabilities, and its implementation according to this standard. This standard is based on IEEE Std 11073-20601, which in turn draws information from both ISO/IEEE 11073-10201 [B6] and ISO/IEEE 11073-20101 [B7]. 2 The medical device encoding rules (MDER) used within this standard are fully described in IEEE Std 11073-20601. The object classes and attributes in this standard are referenced using nomenclature codes. Each code is identified by a reference identifier (RefID). By using a consistent nomenclature, interoperability is enhanced as all implementations maintain the same semantic meaning for the numeric codes. This standard leverages the existing nomenclature codes in IEEE Std 11073-10101™. Meanwhile, it defines specialized nomenclature codes that will be collected in future revisions of IEEE Std 11073-10101. Between this standard, IEEE Std 11073-10101, IEEE Std 11073-20601, and other IEEE Std 11073-104zz, all required nomenclature codes for implementation are documented. New codes may be defined in newer versions/revisions of each of these documents. In the case of a conflict, where one term code has been assigned to two separate semantic concepts with different RefIDs, in general the oldest definition that is in actual use should take precedence. The same policy applies when one RefID has two different code values assigned in different specifications. The resolution of such conflicts will be determined through joint action by the responsible working groups and other stakeholders, and any corrective action will be published as corrigenda. NOTE—In this standard, IEEE Std 11073-104zz is used to refer to the collection of device specialization standards that utilize IEEE Std 11073-20601, where zz can be any number from 01 to 99, inclusive.3 1.4 Word usage The word shall indicates mandatory requirements strictly to be followed in order to conform to the standard and from which no deviation is permitted (shall equals is required to).4,5 The word should indicates that among several possibilities one is recommended as particularly suitable, without mentioning or excluding others; or that a certain course of action is preferred but not necessarily required (should equals is recommended that). The word may is used to indicate a course of action permissible within the limits of the standard (may equals is permitted to). The word can is used for statements of possibility and capability, whether material, physical, or causal (can equals is able to).
35.240.80 Informatikai alkalmazások az egészségügyben
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idt ISO/IEEE 11073-10420:2022; idt EN ISO/IEEE 11073-10420:2022
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