iTeh StandardsiTeh Standards
EURUSD
Your shopping cart is empty.
CEN

ENV 13735:2000

(Main)

Health informatics - Interoperability of patient connected medical devices

Health informatics - Interoperability of patient connected medical devices

This European standard applies to patient connected medical devices that can communicate patient related physiological data between devices and between a device and a computer system. Examples of applicable devices rea given in appendix E. This standard specifies a communication controller model that should be used by applicable devices. This standard states applicable references or specifies protocols including the ACSE, ROSE, CMDISE, presentation and session layer protocols that shall be used by applicable devices.

Zdravstvena informatika – Medobratovalnost medicinskih naprav, priključenih na pacienta

General Information

Status
Withdrawn
Publication Date
19-Sep-2000
Withdrawal Date
26-Jul-2010
ICS
35.240.80 - IT applications in health care technology
Technical Committee
CEN/TC 251 - Medical informatics
Drafting Committee
CEN/TC 251/WG 2 - Terminology and knowledge representation
Current Stage
9960 - Withdrawal effective - Withdrawal
Start Date
27-Jul-2010
Completion Date
27-Jul-2010
Ref Project
SIST ENV 13735:2003 - Health informatics - Interoperability of patient connected medical devices

Buy Standard

ENV 13735:2003ENV 13735:2003
PreviousNext
Standardization document
ENV 13735:2003
English language
175 pages
sale 10% off
Preview
sale 10% off
Preview
e-Library read for
1 day

Standards Content (Sample)

SLOVENSKI STANDARD
SIST ENV 13735:2003
01-oktober-2003
=GUDYVWYHQDLQIRUPDWLND±0HGREUDWRYDOQRVWPHGLFLQVNLKQDSUDYSULNOMXþHQLKQD
SDFLHQWD
Health informatics - Interoperability of patient connected medical devices
Ta slovenski standard je istoveten z: ENV 13735:2000
ICS:
35.240.80 Uporabniške rešitve IT v IT applications in health care
zdravstveni tehniki technology
SIST ENV 13735:2003 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

---------------------- Page: 1 ----------------------

SIST ENV 13735:2003

---------------------- Page: 2 ----------------------

SIST ENV 13735:2003

---------------------- Page: 3 ----------------------

SIST ENV 13735:2003

---------------------- Page: 4 ----------------------

SIST ENV 13735:2003

---------------------- Page: 5 ----------------------

SIST ENV 13735:2003

---------------------- Page: 6 ----------------------

SIST ENV 13735:2003

---------------------- Page: 7 ----------------------

SIST ENV 13735:2003

---------------------- Page: 8 ----------------------

SIST ENV 13735:2003

---------------------- Page: 9 ----------------------

SIST ENV 13735:2003

---------------------- Page: 10 ----------------------

SIST ENV 13735:2003

---------------------- Page: 11 ----------------------

SIST ENV 13735:2003

---------------------- Page: 12 ----------------------

SIST ENV 13735:2003

---------------------- Page: 13 ----------------------

SIST ENV 13735:2003

---------------------- Page: 14 ----------------------

SIST ENV 13735:2003

---------------------- Page: 15 ----------------------

SIST ENV 13735:2003

---------------------- Page: 16 ----------------------

SIST ENV 13735:2003

---------------------- Page: 17 ----------------------

SIST ENV 13735:2003

---------------------- Page: 18 ----------------------

SIST ENV 13735:2003

---------------------- Page: 19 ----------------------

SIST ENV 13735:2003

---------------------- Page: 20 ----------------------

SIST ENV 13735:2003

---------------------- Page: 21 ----------------------

SIST ENV 13735:2003

---------------------- Page: 22 ----------------------

SIST ENV 13735:2003

---------------------- Page: 23 ----------------------

SIST ENV 13735:2003

---------------------- Page: 24 ----------------------

SIST ENV 13735:2003

---------------------- Page: 25 ----------------------

SIST ENV 13735:2003

---------------------- Page: 26 ----------------------

SIST ENV 13735:2003

---------------------- Page: 27 ----------------------

SIST ENV 13735:2003

---------------------- Page: 28 ----------------------

SIST ENV 13735:2003

---------------------- Page: 29 ----------------------

SIST ENV 13735:2003

---------------------- Page: 30 ----------------------

SIST ENV 13735:2003

---------------------- Page: 31 ----------------------

SIST ENV 13735:2003

---------------------- Page: 32 ----------------------

SIST ENV 13735:2003

---------------------- Page: 33 ----------------------

SIST ENV 13735:2003

---------------------- Page: 34 ----------------------

SIST ENV 13735:2003

---------------------- Page: 35 ----------------------

SIST ENV 13735:2003

---------------------- Page: 36 ----------------------

SIST ENV 13735:2003

---------------------- Page: 37 ----------------------

SIST ENV 13735:2003

---------------------- Page: 38 ----------------------

SIST ENV 13735:2003

---------------------- Page: 39 ----------------------

SIST ENV 13735:2003

---------------------- Page: 40 ----------------------

SIST ENV 13735:2003

---------------------- Page: 41 ----------------------

SIST ENV 13735:2003

---------------------- Page: 42 ----------------------

SIST ENV 13735:2003

---------------------- Page: 43 ----------------------

SIST ENV 13735:2003

---------------------- Page: 44 ----------------------

SIST ENV 13735:2003

---------------------- Page: 45 ----------------------

SIST ENV 13735:2003

---------------------- Page: 46 ----------------------

SIST ENV 13735:2003

---------------------- Page: 47 ----------------------

SIST ENV 13735:2003

---------------------- Page: 48 ----------------------

SIST ENV 13735:2003

---------------------- Page: 49 ----------------------

SIST ENV 13735:2003

---------------------- Page: 50 ----------------------

SIST ENV 13735:2003

---------------------- Page: 51 ----------------------

SIST ENV 13735:2003

---------------------- Page: 52 ----------------------

SIST ENV 13735:2003

---------------------- Page: 53 ----------------------

SIST ENV 13735:2003

---------------------- Page: 54 ----------------------

SIST ENV 13735:2003

---------------------- Page: 55 ----------------------

SIST ENV 13735:2003

---------------------- Page: 56 ----------------------

SIST ENV 13735:2003

---------------------- Page: 57 ----------------------

SIST ENV 13735:2003

---------------------- Page: 58 ----------------------

SIST ENV 13735:2003

---------------------- Page: 59 ----------------------

SIST ENV 13735:2003

---------------------- Page: 60 ----------------------

SIST ENV 13735:2003

---------------------- Page: 61 ----------------------

SIST ENV 13735:2003

---------------------- Page: 62 ----------------------

SIST ENV 13735:2003

---------------------- Page: 63 ----------------------

SIST ENV 13735:2003

---------------------- Page: 64 ----------------------

SIST ENV 13735:2003

---------------------- Page: 65 ----------------------

SIST ENV 13735:2003

---------------------- Page: 66 ----------------------

SIST ENV 13735:2003

---------------------- Page: 67 ----------------------

SIST ENV 13735:2003

---------------------- Page: 68 ----------------------

SIST ENV 13735:2003

---------------------- Page: 69 ----------------------

SIST ENV 13735:2003

---------------------- Page: 70 ----------------------

SIST ENV 13735:2003

---------------------- Page: 71 ----------------------

SIST ENV 13735:2003

---------------------- Page: 72 ----------------------

SIST ENV 13735:2003

---------------------- Page: 73 ----------------------

SIST ENV 13735:2003

---------------------- Page: 74 ----------------------

SIST ENV 13735:2003

---------------------- Page: 75 ----------------------

SIST ENV 13735:2003

---------------------- Page: 76 ----------------------

SIST ENV 13735:2003

---------------------- Page: 77 ----------------------

SIST ENV 13735:2003

---------------------- Page: 78 ----------------------

SIST ENV 13735:2003

---------------------- Page: 79 ----------------------

SIST ENV 13735:2003

---------------------- Page: 80 ----------------------

SIST ENV 13735:2003

---------------------- Page: 81 ----------------------

SIST ENV 13735:2003

---------------------- Page: 82 ----------------------

SIST ENV 13735:2003

---------------------- Page: 83 ----------------------

SIST ENV 13735:2003

---------------------- Page: 84 ----------------------

SIST ENV 13735:2003

---------------------- Page: 85 ----------------------

SIST ENV 13735:2003

---------------------- Page: 86 ----------------------

SI
...

Questions, Comments and Discussion

Ask us and Technical Secretary will try to provide an answer. You can facilitate discussion about the standard in here.

This May Also Interest You

CEN
EN ISO 17117-1:2023(Main)
Health informatics - Terminological resources - Part 1: Characteristics (ISO 17117-1:2018)
oSIST prEN ISO 17117-1:2023

ISO 17117-1:2018 defines universal and specialized characteristics of health terminological resources that make them fit for the purposes required of various applications. It refers only to terminological resources that are primarily designed to be used for clinical concept representation or to those parts of other terminological resources designed to be used for clinical concept representation.
ISO 17117-1:2018 helps users to assess whether a terminology has the characteristics or provides the functions that will support their specified requirements. The focus of this document is to define characteristics and functions of terminological resources in healthcare that can be used to identify different types of them for categorization purposes. Clauses 4 and 5 support categorization according to the characteristics and functions of the terminological resources rather than the name.
NOTE       Categorization of healthcare terminological systems according to the name of the system might not be helpful and has caused confusion in the past.
The target groups for this document are:
a)    organizations wishing to select terminological systems for use in healthcare information systems;
b)    developers of terminological systems;
c)    developers of terminology standards;
d)    those undertaking independent evaluations/academic reviews of terminological resources;
e)    terminology Registration Authorities.
ISO 17117-1:2018 contains general characteristics and criteria with which systems can be evaluated.
The following considerations are outside the scope of this document.
-      Evaluations of terminological resources.
-      Health service requirements for terminological resources and evaluation criteria based on the characteristics and functions.
-      The nature and quality of mappings between different terminologies. It is unlikely that a single terminology will meet all the terminology requirements of a healthcare organization: some terminology providers produce mappings to administrative or statistical classifications such as the International Classification of Diseases (ICD). The presence of such maps would be a consideration in the evaluation of the terminology.
-      The nature and quality of mappings between different versions of the same terminology. To support data migration and historical retrieval, terminology providers can provide maps between versions of their terminology. The presence of such maps would be a consideration in the evaluation of the terminology.
-      Terminology server requirements and techniques and tools for terminology developers.
-      Characteristics for computational biology terminology. Progress in medical science and in terminology science will necessitate updating of this document in due course.

  • Draft
    35 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
EN ISO 11239:2023(Main)
Health informatics - Identification of medicinal products - Data elements and structures for the unique identification and exchange of regulated information on pharmaceutical dose forms, units of presentation, routes of administration and packaging (ISO 11239:2023)
SIST EN ISO 11239:2023

This document specifies:
—     the data elements, structures and relationships between the data elements required for the exchange of information, which uniquely and with certainty identify pharmaceutical dose forms, units of presentation, routes of administration and packaging items (containers, closures and administration devices) related to medicinal products;
—     a mechanism for the association of translations of a single concept into different languages, which is an integral part of the information exchange;
—     a mechanism for the versioning of the concepts in order to track their evolution;
—     rules to help regional authorities to map existing regional terms to the terms created using this document, in a harmonized and meaningful way.

  • Standard
    37 pages
    English language
    sale 10% off
    e-Library read for
    1 day
  • Draft
    34 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
CEN ISO/TS 20440:2023(Main)
Health informatics - Identification of medicinal products - Implementation guidelines for ISO 11239 data elements and structures for the unique identification and exchange of regulated information on pharmaceutical dose forms, units of presentation, routes of administration and packaging (ISO/TS 20440:2023)
SIST-TS CEN ISO/TS 20440:2023

This document describes data elements and structures for the unique identification and exchange of regulated information on pharmaceutical dose forms, units of presentation, routes of administration and packaging.
Based on the principles outlined in this document, harmonised controlled terminologies will be developed according to an agreed maintenance process, allowing users to consult the terminologies and locate the appropriate terms for the concepts that they wish to describe. Provisions to allow for the mapping of existing regional terminologies to the harmonised controlled terminologies will also be developed in order to facilitate the identification of the appropriate terms. The codes provided for the terms can then be used in the relevant fields in the PhPID, PCID and MPID in order to identify those concepts.
This document is intended for use by:
—    any organization that might be responsible for developing and maintaining such controlled vocabularies;
—    any regional authorities or software vendors who want to use the controlled vocabularies in their own systems and need to understand how they are created;
—    owners of databases who want to map their own terms to a standardized list of controlled vocabularies;
—    other users who want to understand the hierarchy of the controlled vocabularies in order to help identify the most appropriate term to describe a particular concept.
This document does not specify a particular terminology for the implementation of ISO 11239.

  • Technical specification
    53 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
EN ISO/IEEE 11073-10408:2022(Main)
Health informatics - Device interoperability - Part 10408: Personal health device communication - Device specialization - Thermometer (ISO/IEEE 11073-10408:2022)
SIST EN ISO/IEEE 11073-10408:2023

Within the context of the ISO/IEEE 11073 family of standards for device communication, this document establishes a normative definition of communication between personal telehealth thermometer devices and compute engines (e.g., cell phones, personal computers, personal health appliances, and 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 document defines a common core of communication functionality for personal telehealth thermometer devices.

  • Standard
    60 pages
    English language
    sale 10% off
    e-Library read for
    1 day
  • Draft
    57 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
EN ISO/IEEE 11073-10404:2022(Main)
Health informatics - Device interoperability - Part 10404: Personal health device communication - Device specialization - Pulse oximeter (ISO/IEEE 11073-10404:2022)
SIST EN ISO/IEEE 11073-10404:2023

Within the context of the ISO/IEEE 11073 family of standards for device communication, this document establishes a normative definition of communication between personal telehealth pulse oximetry 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 document defines a common core of communication functionality for personal telehealth pulse oximeters.

  • Standard
    87 pages
    English language
    sale 10% off
    e-Library read for
    1 day
  • Draft
    85 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
EN ISO/IEEE 11073-10407:2022(Main)
Health informatics - Device interoperability - Part 10407: Personal health device communication - Device specialization - Blood pressure monitor (ISO/IEEE 11073-10407:2022)
SIST EN ISO/IEEE 11073-10407:2023

Within the context of the ISO/IEEE 11073 family of standards for device communication, this document establishes a normative definition of communication between personal telehealth blood pressure monitor devices and compute engines (e.g., cell phones, personal computers, personal health appliances, and 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 document defines a common core of communication functionality for personal telehealth blood pressure monitors.

  • Standard
    73 pages
    English language
    sale 10% off
    e-Library read for
    1 day
  • Draft
    70 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
EN ISO/IEEE 11073-10420:2022(Main)
Health informatics - Device interoperability - Part 10420: Personal health device communication - Device specialization - Body composition analyzer (ISO/IEEE 11073-10420:2022)
SIST EN ISO/IEEE 11073-10420:2023

Within the context of the ISO/IEEE 11073 family of standards for device communication, 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) is established by this document 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 document 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.

  • Standard
    82 pages
    English language
    sale 10% off
    e-Library read for
    1 day
  • Draft
    79 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
EN ISO/IEEE 11073-10415:2022(Main)
Health informatics - Device interoperability - Part 10415: Personal health device communication - Device specialization - Weighing scale (ISO/IEEE 11073-10415:2022)
SIST EN ISO/IEEE 11073-10415:2023

Within the context of the ISO/IEEE 11073 family of standards for device communication, this document establishes a normative definition of communication between personal telehealth weighing scale devices and compute engines (e.g., cell phones, personal computers, personal health appliances, and 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 document defines a common core of communication functionality for personal telehealth weighing scales.

  • Standard
    64 pages
    English language
    sale 10% off
    e-Library read for
    1 day
  • Draft
    61 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
EN ISO/IEEE 11073-20601:2022(Main)
Health informatics - Device interoperability - Part 20601: Personal health device communication - Application profile - Optimized exchange protocol (ISO/IEEE 11073-20601:2022)
SIST EN ISO/IEEE 11073-20601:2023

Within the context of the ISO/IEEE 11073 personal health device standard family, this document defines an optimized exchange protocol and modeling techniques to be used by implementers of personal health devices to create interoperability between device types and vendors. This document establishes a common framework for an abstract model of personal health data available in transport-independent transfer syntax required to establish logical connections between systems and to provide presentation capabilities and services needed to perform communication tasks. The protocol is optimized to personal health usage requirements and leverages commonly used methods and tools wherever possible.

  • Standard
    287 pages
    English language
    sale 10% off
    e-Library read for
    1 day
  • Draft
    284 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
CEN ISO/TS 17251:2023(Main)
Health informatics - Business requirements for a syntax to exchange structured dose information for medicinal products (ISO/TS 17251:2023)
SIST-TS CEN ISO/TS 17251:2023

This document specifies the business requirements for the structured content of structured or semi-
structured dose instructions for recording dose instructions in the electronic health record (EHR),
supporting clinical decision support, and in exchanging medication orders, as applicable to primary,
secondary and tertiary care.
This document is focused on the dose instructions as will be presented to the individual subject of care
or caregiver. Comprehension of dose instructions by the subject of care or caregiver is an overarching
consideration for subject of care safety and the best outcomes. Related factors are discussed but are not
part of the primary scope.
This document does not define an information model, except to the extent that those information model
concepts are necessary to define business requirements.
Outside the scope of this document are:
— The implementation of dose instructions, i.e. assembling the structured elements into a form
appropriate for the patient or caregiver;
— The content of a medication order (see ISO 17523) beyond content related to dose instructions;
— The content of a record of dispense of a medicinal product (see ISO/TS 19293);
— The functionality of health, clinical and/or pharmacy systems;
— Other kinds of content of health, clinical or pharmacy systems that are needed to support the whole
process of health care providers, such as:
— A drug knowledge database (see ISO/TS 22756);
— A decision support system (see ISO/TS 22756 and ISO/TS 22703);
— A complete medical record (EHR);
— A medicinal product dictionary (see ISO/TS 19256);
— Verification of the medicinal product and dose being administered.
— Some concepts from Identification of Medicinal Products are referenced, but not defined, in this
document. See Clause 4 for discussion of the relationship of this document with IDMP.

  • Technical specification
    23 pages
    English language
    sale 10% off
    e-Library read for
    1 day