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BS EN ISO 11073-10472:2012

BS EN ISO 11073-10472:2012

$215.11

Health Informatics. Personal health device communication – Device specialization. Medication monitor

Published By Publication Date Number of Pages
BSI 2012 80
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Within the context of the ISO/IEEE 11073 family of standards for device communication, this standard establishes a normative definition of the communication between medication monitoring devices 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 and information models. It specifies the use of specific term codes, formats, and behaviors in telehealth environments restricting ambiguity in base frameworks in favor of interoperability. This standard defines a common core of communication functionality for medication monitors. In this context, medication monitors are defined as devices that have the ability to determine and communicate (to a manager) measures of a user’s adherence to a medication regime.

PDF Catalog

PDF Pages PDF Title
5 Contents
7 Foreword
9 Introduction
11 1. Overview
1.1 Scope
12 1.2 Purpose
1.3 Context
2. Normative references
3. Definitions, acronyms, and abbreviations
13 3.1 Definitions
3.2 Acronyms and abbreviations
14 4. Introduction to ISO/IEEE 11073 personal health devices
4.1 General
4.2 Introduction to IEEE 11073-20601 modeling constructs
4.2.1 General
4.2.2 Domain information model
4.2.3 Service model
4.2.4 Communication model
15 4.2.5 Implementing the models
5. Medication monitor device concepts and modalities
5.1 General
16 5.2 Model usage examples
5.2.1 General
5.2.2 Sequenced medication monitor example types
17 5.2.3 Non-sequenced medication monitor example types
5.3 Medication dispensed
18 5.4 Status reporter
5.5 User feedback
19 5.6 Usage patterns
6. Medication monitor domain information model
6.1 Overview
6.2 Class extensions
20 6.3 Object instance diagram
21 6.4 Types of configuration
6.4.1 General
6.4.2 Standard configuration
22 6.4.3 Extended configuration
6.5 Medical device system object
6.5.1 MDS object attributes
23 6.5.2 MDS object methods
24 6.5.3 MDS object events
25 6.5.4 Other MDS services
26 6.6 Numeric objects
6.6.1 General
6.6.2 Fixed-dosage medication dispensed
28 6.6.3 Variable-dosage medication dispensed
30 6.6.4 User feedback
32 6.7 Real-time sample array objects
6.8 Enumeration objects
6.8.1 General
33 6.8.2 Status reporter
37 6.9 PM-store objects
6.9.1 General
38 6.9.2 Persistent store model
6.9.3 PM-store object attributes
39 6.9.4 PM-store object methods
6.9.5 PM-store object events
40 6.9.6 PM-store object services
6.9.7 PM-segment objects
6.10 Scanner objects
41 6.11 Class extension objects
6.12 Medication monitor information model extensibility rules
7. Medication monitor service model
7.1 General
7.2 Object access services
42 7.3 Object access event report services
43 8. Medication monitor communication model
8.1 Overview
8.2 Communications characteristics
8.3 Association procedure
8.3.1 General
8.3.2 Agent procedure—association request
44 8.3.3 Manager procedure—association response
45 8.4 Configuring procedure
8.4.1 General
8.4.2 Medication monitor—standard configurations
51 8.5 Operating procedure
8.5.1 General
8.5.2 GET medication monitor MDS attributes
52 8.5.3 Measurement data transmission
8.6 Time synchronization
9. Test associations
9.1 Behavior with standard configuration
53 9.2 Behavior with extended configurations
10. Conformance
10.1 Applicability
10.2 Conformance specification
54 10.3 Levels of conformance
10.3.1 General
10.3.2 Conformance level 1: Base conformance
10.3.3 Conformance level 2: Extended nomenclature (ASN.1 and/or ISO/IEEE 11073-10101:2004 [B1])
10.4 Implementation conformance statements
10.4.1 General format
55 10.4.2 General implementation conformance statement
57 10.4.3 DIM MOC implementation conformance statement
10.4.4 MOC attribute ICS
58 10.4.5 MOC notification implementation conformance statement
59 10.4.6 MOC nomenclature conformance statement
60 Annex A (informative) Bibliography
61 Annex B (normative) Any additional ASN.1 definitions
62 Annex C (normative) Allocation of identifiers
63 Annex D (informative) Message sequence examples
65 Annex E (informative) Protocol data unit examples
E.1 General
E.2 Association information exchange
E.2.1 General
E.2.2 Extended configuration
E.2.2.1 General
E.2.2.2 Association request
66 E.2.2.3 Association response
E.2.3.1 General
E.2.3.2 Association request
67 E.2.3.3 Association response
E.2.4 Standard configuration
E.2.4.1 General
E.2.4.2 Association request
68 E.2.4.3 Association response
E.3 Configuration information exchange
E.3.1 General
69 E.3.2 Extended configuration
E.3.2.1 General
E.3.2.2 Remote operation invoke event report configuration
E.3.2.3 Remote operation response event report configuration
70 E.3.3 Known configuration
E.3.3.1 General
E.3.3.2 Remote operation invoke event report configuration
E.3.3.3 Remote operation response event report configuration
E.3.4 Standard configuration
E.3.4.1 General
E.3.4.2 Remote operation invoke event report configuration
E.3.4.3 Remote operation response event report configuration
71 E.4 GET MDS attributes service
E.4.1.1 General
E.4.1.2 Get all medical device system attributes request
E.4.1.3 Get response with all MDS attributes
72 E.5 Data reporting
E.5.1 Confirmed measurement data transmission
E.5.2 Response to confirmed measurement data transmission
73 E.6 Disassociation
E.6.1 Association release request
E.6.2 Association release response
74 Annex F (informative) IEEE list of participants

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BS EN ISO 11073-10472:2012
$215.11