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IEEE ISO 11073 10472 2010

IEEE ISO 11073 10472 2010

$94.79

Health informatics–Personal health device communication–Part 10472: Device specialization–Medication monitor

Published By Publication Date Number of Pages
IEEE 2010 75
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New IEEE Standard – Active. Within the context of the ISO/IEEE 11073 family of standards for device communication, this standard establishes a normative definition of communication between personal telehealth medication monitor devices and compute engines (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 restricting optionality in base frameworks in favor of interoperability. This standard defines a common core of communication functionality for personal telehealth medication monitor devices.

PDF Catalog

PDF Pages PDF Title
1 IEEE Std 11073-10472-2010 cover page
3 IEEE Std 11073-10472-2010 title page
6 Introduction
Notice to users
Laws and regulations
Copyrights
Updating of IEEE documents
7 Errata
Interpretations
Patents
8 Participants
11 Contents
13 Important Notice
1. Overview
1.1 Scope
14 1.2 Purpose
1.3 Context
2. Normative references
3. Definitions, acronyms, and abbreviations
15 3.1 Definitions
3.2 Acronyms and abbreviations
16 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
17 4.2.5 Implementing the models
5. Medication monitor device concepts and modalities
5.1 General
18 5.2 Model usage examples
5.2.1 General
5.2.2 Sequenced medication monitor example types
19 5.2.3 Non-sequenced medication monitor example types
5.3 Medication dispensed
20 5.4 Status reporter
5.5 User feedback
21 5.6 Usage patterns
6. Medication monitor domain information model
6.1 Overview
6.2 Class extensions
22 6.3 Object instance diagram
23 6.4 Types of configuration
6.4.1 General
6.4.2 Standard configuration
24 6.4.3 Extended configuration
6.5 Medical device system object
6.5.1 MDS object attributes
25 6.5.2 MDS object methods
26 6.5.3 MDS object events
27 6.5.4 Other MDS services
28 6.6 Numeric objects
6.6.1 General
6.6.2 Fixed-dosage medication dispensed
30 6.6.3 Variable-dosage medication dispensed
32 6.6.4 User feedback
34 6.7 Real-time sample array objects
6.8 Enumeration objects
6.8.1 General
35 6.8.2 Status reporter
39 6.9 PM-store objects
6.9.1 General
40 6.9.2 Persistent store model
6.9.3 PM-store object attributes
41 6.9.4 PM-store object methods
6.9.5 PM-store object events
42 6.9.6 PM-store object services
6.9.7 PM-segment objects
6.10 Scanner objects
43 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
44 7.3 Object access event report services
45 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
46 8.3.3 Manager procedure—association response
47 8.4 Configuring procedure
8.4.1 General
8.4.2 Medication monitor—standard configurations
53 8.5 Operating procedure
8.5.1 General
8.5.2 GET medication monitor MDS attributes
54 8.5.3 Measurement data transmission
8.6 Time synchronization
9. Test associations
9.1 Behavior with standard configuration
55 9.2 Behavior with extended configurations
10. Conformance
10.1 Applicability
10.2 Conformance specification
56 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
57 10.4.2 General implementation conformance statement
59 10.4.3 DIM MOC implementation conformance statement
10.4.4 MOC attribute ICS
60 10.4.5 MOC notification implementation conformance statement
61 10.4.6 MOC nomenclature conformance statement
62 Annex A (informative) Bibliography
63 Annex B (normative) Any additional ASN.1 definitions
64 Annex C (normative) Allocation of identifiers
65 Annex D (informative) Message sequence examples
67 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
68 E.2.2.3 Association response
E.2.3.1 General
E.2.3.2 Association request
69 E.2.3.3 Association response
E.2.4 Standard configuration
E.2.4.1 General
E.2.4.2 Association request
70 E.2.4.3 Association response
E.3 Configuration information exchange
E.3.1 General
71 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
72 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
73 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
74 E.5 Data reporting
E.5.1 Confirmed measurement data transmission
E.5.2 Response to confirmed measurement data transmission
75 E.6 Disassociation
E.6.1 Association release request
E.6.2 Association release response

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IEEE ISO 11073 10472 2010
$94.79