
EN ISO 11073-10425:2016
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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Health informatics - Personal health device communication - Part 10425: Device specialization - Continuous glucose monitor (CGM) (ISO 11073-10425:2016)
01-31-2017
06-29-2016
European foreword
1 Overview
2 Normative references
3 Definitions, acronyms, and abbreviations
4 Introduction to IEEE 11073[TM] personal health devices
5 Glucose monitoring concepts and modalities
6 Continuous glucose monitor domain information model
7 Continuous glucose monitor service model
8 Continuous glucose monitor communication model
9 Test associations
10 Conformance
Annex A (informative) - Bibliography
Annex B (normative) - Any additional ASN.1 definitions
Annex C (normative) - Allocation of identifiers
Annex D (informative) - Message sequence examples
Annex E (informative) - Protocol data unit examples
This standard establishes a normative definition of communication between personal health continuous glucose monitor (CGM) devices (agents) and managers [e.g., cell phones, personal computers (PCs), personal health appliances, set top boxes] in a manner that enables plug-and-play interoperability. It leverages work done in other ISO/IEEE 11073 standards including existing terminology, informationprofiles, 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 of CGM devices. In this context, CGM refers to the measurement of the level of glucose in the body on a regular (typically 5 minute) basis through a sensor continuously attached to the person.
Committee |
CEN/TC 251
|
DocumentType |
Standard
|
PublisherName |
Comite Europeen de Normalisation
|
Status |
Superseded
|
SupersededBy |
Standards | Relationship |
UNE-EN ISO 11073-10425:2016 | Identical |
I.S. EN ISO 11073-10425:2019 | Identical |
BS EN ISO 11073-10425:2019 | Identical |
DIN EN ISO 11073-10425:2016-10 | Identical |
NF EN ISO 11073-10425 : 2016 | Identical |
NEN EN ISO/IEEE 11073-10425 : 2016 | Identical |
DIN EN ISO 11073-10425:2018-11 (Draft) | Identical |
UNI EN ISO 11073-10425:2019 | Identical |
SN EN ISO 11073-10425 : 2016 | Identical |
ISO/IEEE 11073-10425:2016 | Identical |
I.S. EN ISO 11073-10425:2016 | Identical |
PN-EN ISO 11073-10425 : 2019-05 | Identical |
ISO/IEEE 11073-10425:2019 | Identical |
PN EN ISO 11073-10425 : 2016 | Identical |
UNI EN ISO 11073-10425 : 2017 | Identical |
ONORM EN ISO 11073-10425 : 2016 | Identical |
NEN-EN-ISO/IEEE 11073-10425:2019 en | Identical |
BS EN ISO 11073-10425:2016 | Identical |
IEC 80001-1:2010 | Application of risk management for IT-networks incorporating medical devices - Part 1: Roles, responsibilities and activities |
IEC 60601-1:2005+AMD1:2012 CSV | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
ISO/IEEE 11073-20101:2004 | Health informatics — Point-of-care medical device communication — Part 20101: Application profiles — Base standard |
IEC 62304:2006+AMD1:2015 CSV | Medical device software - Software life cycle processes |
ISO/IEEE 11073-20601:2016 | Health informatics — Personal health device communication — Part 20601: Application profile — Optimized exchange protocol |
ISO 14971:2007 | Medical devices Application of risk management to medical devices |
ISO/IEEE 11073-10101:2004 | Health informatics — Point-of-care medical device communication — Part 10101: Nomenclature |
IEEE 11073-20601A : 2010 | HEALTH INFORMATICS - PERSONAL HEALTH DEVICE COMMUNICATION - PART 20601: APPLICATION PROFILE - OPTIMIZED EXCHANGE PROTOCOL - AMENDMENT 1 |
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