iTeh StandardsiTeh Standards
EURUSD
Your shopping cart is empty.
CEN

EN ISO 11073-10101:2005

(Main)

Health informatics - Point-of-care medical device communication - Part 10101: Nomenclature (ISO/IEEE 11073-10101:2004)

Health informatics - Point-of-care medical device communication - Part 10101: Nomenclature (ISO/IEEE 11073-10101:2004)

ISO 11073-10101:2004 covers nomenclature architecture for point-of-care (POC) medical device communication (MDC).
It defines the overall architecture of the organization and relationships among nomenclature components and provides specifications of semantics and syntaxes.
ISO 11073-10101:2004 is intended for use within the context of IEEE Std 1073,1 which sets out the relationship between this and other documents in the POC MDC series.

Medizinische Informatik - Kommunikation patientennaher medizinischer Geräte - Teil 10101: Nomenklatur

Informatique de santé - Communication entre dispositifs médicaux sur le site des soins - Partie 10101: Nomenclature (ISO/IEEE 11073-10101:2004)

Zdravstvena informatika – Komunikacija medicinskih naprav na mestu oskrbe – 10101. del: Nomenklatura (ISO/IEEE 11073-10101:2004)

General Information

Status
Withdrawn
Publication Date
30-Aug-2005
Withdrawal Date
22-Sep-2020
ICS
01.040.35 - Information technology (Vocabularies)
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
Completion Date
23-Sep-2020
Ref Project
SIST EN ISO 11073-10101:2005 - Health informatics - Point-of-care medical device communication - Part 10101: Nomenclature (ISO/IEEE 11073-10101:2004)

Relations

Replaced By
EN ISO 11073-10101:2020 - Health informatics - Device interoperability - Part 10101: Point-of-care medical device communication - Nomenclature (ISO/IEEE 11073-10101:2020)
Effective Date
30-Sep-2020
Amended By
EN ISO 11073-10101:2005/A1:2017 - Health informatics - Point-of-care medical device communication - Part 10101: Nomenclature - Amendment 1: Additional definitions (ISO/IEEE 11073-10101:2004/Amd 1:2017)
Effective Date
08-Jun-2022

Buy Standard

EN ISO 11073-10101:2005EN ISO 11073-10101:2005
PreviousNext
Standard
EN ISO 11073-10101:2005
English language
503 pages
sale 10% off
Preview
sale 10% off
Preview
e-Library read for
1 day

Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN ISO 11073-10101:2005
01-november-2005
Zdravstvena informatika – Komunikacija medicinskih naprav na mestu oskrbe –
10101. del: Nomenklatura (ISO/IEEE 11073-10101:2004)
Health informatics - Point-of-care medical device communication - Part 10101:
Nomenclature (ISO/IEEE 11073-10101:2004)
Medizinische Informatik - Kommunikation patientennaher medizinischer Geräte - Teil
10101: Nomenklatur
Informatique de santé - Communication entre dispositifs médicaux sur le site des soins -
Partie 10101: Nomenclature (ISO/IEEE 11073-10101:2004)
Ta slovenski standard je istoveten z: EN ISO 11073-10101:2005
ICS:
35.240.80 Uporabniške rešitve IT v IT applications in health care
zdravstveni tehniki technology
SIST EN ISO 11073-10101:2005 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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

SIST EN ISO 11073-10101:2005

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

SIST EN ISO 11073-10101:2005
EUROPEAN STANDARD
EN ISO 11073-10101
NORME EUROPÉENNE
EUROPÄISCHE NORM
August 2005
ICS 35.240.80; 01.040.35

English Version
Health informatics - Point-of-care medical device communication
- Part 10101: Nomenclature (ISO/IEEE 11073-10101:2004)
Informatique de santé - Communication entre dispositifs Medizinische Informatik - Kommunikation patientennaher
médicaux sur le site des soins - Partie 10101: medizinischer Geräte - Teil 10101: Nomenklatur
Nomenclature (ISO/IEEE 11073-10101:2004)
This European Standard was approved by CEN on 16 August 2005.
CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this European
Standard the status of a national standard without any alteration. Up-to-date lists and bibliographical references concerning such national
standards may be obtained on application to the Central Secretariat or to any CEN member.
This European Standard exists in three official versions (English, French, German). A version in any other language made by translation
under the responsibility of a CEN member into its own language and notified to the Central Secretariat has the same status as the official
versions.
CEN members are the national standards bodies of Austria, Belgium, Cyprus, Czech Republic, Denmark, Estonia, Finland, France,
Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Slovakia,
Slovenia, Spain, Sweden, Switzerland and United Kingdom.
EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION
EUROPÄISCHES KOMITEE FÜR NORMUNG
Management Centre: rue de Stassart, 36  B-1050 Brussels
© 2005 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 11073-10101:2005: E
worldwide for CEN national Members.

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

SIST EN ISO 11073-10101:2005
EN ISO 11073-10101:2005 (E)






Foreword



The text of ISO/IEEE 11073-10101:2004 has been prepared by Technical Committee ISO/TC
215 "Health informatics” of the International Organization for Standardization (ISO) and has
been taken over as EN ISO 11073-10101:2005 by Technical Committee CEN/TC 251 "Health
informatics", the secretariat of which is held by NEN.

This European Standard shall be given the status of a national standard, either by publication of
an identical text or by endorsement, at the latest by February 2006, and conflicting national
standards shall be withdrawn at the latest by February 2006.

According to the CEN/CENELEC Internal Regulations, the national standards organizations of
the following countries are bound to implement this European Standard: Austria, Belgium,
Cyprus, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary,
Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland,
Portugal, Slovakia, Slovenia, Spain, Sweden, Switzerland and United Kingdom.


Endorsement notice

The text of ISO/IEEE 11073-10101:2004 has been approved by CEN as EN ISO 11073-
10101:2005 without any modifications.

2

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

SIST EN ISO 11073-10101:2005
INTERNATIONAL
ISO/IEEE
STANDARD
11073-10101
First edition
2004-12-15
Health informatics — Point-of-care
medical device communication —
Part 10101:
Nomenclature
Informatique de santé — Communication entre dispositifs médicaux sur le
site des soins —
Partie 10101: Nomenclature
Reference number
ISO/IEEE 11073-10101:2004(E)
© ISO/IEEE 2004

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

SIST EN ISO 11073-10101:2005

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

SIST EN ISO 11073-10101:2005
ISO/IEEE 11073-10101:2004(E)
Health informatics — Point-of-care
medical device communication —
Part 10101:
Nomenclature
Sponsor
™
IEEE 1073 Standard Committee
of the
IEEE Engineering in Medicin
...

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 11073-10101:2020(Main)
Health informatics - Device interoperability - Part 10101: Point-of-care medical device communication - Nomenclature (ISO/IEEE 11073-10101:2020)
SIST EN ISO 11073-10101:2021

This document defines a nomenclature for communication of information from point-of-care medical devices. Primary emphasis is placed on acute care medical devices and patient vital signs information. The nomenclature also supports concepts in an object-oriented information model that is for medical device communication.

  • Standard
    1066 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
CEN/TR 15212:2006(Main)
Health informatics - Vocabulary - Maintenance procedure for a web-based terms and concepts database
SIST-TP CEN/TR 15212:2006

This document describes the general requirements on a terms and concepts database. This document also proposes a maintenance procedure for CEN/TC 251, the content, structure and user interface to a web-based terms- and concepts database that will compile the defined concepts with their preferred terms and definitions from the standards developed by
CEN/TC 251. These are terms from the health informatics field and not all terms and concepts used in healthcare.
It also describes an example of an implementation and ends with a proposal for CEN/TC 251 for the establishment and maintenance of such a terms and concepts database.

  • Technical report
    21 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
prEN 13940-2(Main)
Health informatics - System of concepts to support continuity of care - Part 2: Health care process and workflow
oSIST prEN 13940-2:2010

The purpose of this European Standard is to enable communication at the semantic level between information systems in health care. This part standard complements Part 1. Its specific purpose is to define a system of concepts enabling the management, including communication, of the necessary information about the core process of health care provision to an individual subject of care and the corresponding workflow, so as to support its continuity, taking into consideration decision processes, quality control, and resource management. It provides the terminology for planning, delivery and follow-up of those activities that form the overall process.
This part standard applies a process modelling technique to identify the process objects, activities and sub-processes. It also takes into consideration the resource aspects, the responsibilities of health care providers, and means for patients' participation. Whenever continuity of health care delivery implies social interventions as part of, or in support to, the process towards health recovery, these are to be mentioned wherever relevant in the process and workflow; but addressing those social interventions in depth is not part of the scope of this European Standard.

  • Draft
    78 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
EN ISO 11073-10101:2020(Main)
Health informatics - Device interoperability - Part 10101: Point-of-care medical device communication - Nomenclature (ISO/IEEE 11073-10101:2020)
SIST EN ISO 11073-10101:2021

This document defines a nomenclature for communication of information from point-of-care medical devices. Primary emphasis is placed on acute care medical devices and patient vital signs information. The nomenclature also supports concepts in an object-oriented information model that is for medical device communication.

  • Standard
    1066 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
CEN/TR 15212:2006(Main)
Health informatics - Vocabulary - Maintenance procedure for a web-based terms and concepts database
SIST-TP CEN/TR 15212:2006

This document describes the general requirements on a terms and concepts database. This document also proposes a maintenance procedure for CEN/TC 251, the content, structure and user interface to a web-based terms- and concepts database that will compile the defined concepts with their preferred terms and definitions from the standards developed by
CEN/TC 251. These are terms from the health informatics field and not all terms and concepts used in healthcare.
It also describes an example of an implementation and ends with a proposal for CEN/TC 251 for the establishment and maintenance of such a terms and concepts database.

  • Technical report
    21 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
prEN 13940-2(Main)
Health informatics - System of concepts to support continuity of care - Part 2: Health care process and workflow
oSIST prEN 13940-2:2010

The purpose of this European Standard is to enable communication at the semantic level between information systems in health care. This part standard complements Part 1. Its specific purpose is to define a system of concepts enabling the management, including communication, of the necessary information about the core process of health care provision to an individual subject of care and the corresponding workflow, so as to support its continuity, taking into consideration decision processes, quality control, and resource management. It provides the terminology for planning, delivery and follow-up of those activities that form the overall process.
This part standard applies a process modelling technique to identify the process objects, activities and sub-processes. It also takes into consideration the resource aspects, the responsibilities of health care providers, and means for patients' participation. Whenever continuity of health care delivery implies social interventions as part of, or in support to, the process towards health recovery, these are to be mentioned wherever relevant in the process and workflow; but addressing those social interventions in depth is not part of the scope of this European Standard.

  • Draft
    78 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
EN ISO 16739-1:2024(Main)
Industry Foundation Classes (IFC) for data sharing in the construction and facility management industries - Part 1: Data schema (ISO 16739-1:2024)
kSIST FprEN ISO 16739-1:2024

This document represents an open international standard for information used in Building Information Modeling (BIM) that is exchanged and shared among software applications used by the various participants in the construction or facility management industry sector. This document includes definitions that cover information required for buildings and infrastructure works over their life cycle. This edition of the document added coverage of information required for infrastructure facilities including bridges, roads, railways, waterways and port facilities.
This document comprises the publication of a data schema, its documentation, the property and quantity set definitions and the mechanism of an exchange file format structure.
Definitions from this document are used to support different recognized work flows in the construction and facility management industry sector, representing information deliveries. Such information deliveries can be described according to ISO 29481.
Different implementation levels of this document can be defined to better support multiple information deliveries, they are referred to as a Model View Definition (MVD). Each MVD identifies which subset of the definitions of this document imposes requirements for implementation in software applications. Conforming software applications need to identify the model view definition they conform to when applying for software certification.
The following are within the scope of this edition of this document:
BIM exchange format definitions that are required during the life cycle phases of buildings and infrastructure:
demonstrating the need;
conception of need;
outline feasibility;
substantive feasibility study and outline financial authority;
outline conceptual design;
full conceptual design;
coordinated design;
procurement and full financial authority;
production information;
construction;
operation and maintenance.
BIM exchange format definitions that are required by the various disciplines involved within the life cycle phases:
architecture and civil engineering design;
service and utilities engineering;
structural engineering;
procurement;
construction planning;
facility and utility management;
project management;
client requirement management;
industry authorities for permits and approval.
BIM exchange format definitions including:
project structure;
physical components;
spatial components;
analysis items;
processes;
resources;
controls;
actors;
context definition.

  • Draft
    406 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
EN ISO 17294-1:2024(Main)
Water quality - Application of inductively coupled plasma mass spectrometry (ICP-MS) - Part 1: General requirements (ISO 17294-1:2024)
kSIST FprEN ISO 17294-1:2023

This document specifies the principles of inductively coupled plasma mass spectrometry (ICP-MS) and provides general requirements for the use of this technique to determine elements in water, digests of sludges and sediments (e.g. digests of water as described in ISO 15587-1 or ISO 15587-2). Generally, the measurement is carried out in water, but gases, vapours or fine particulate matter can be introduced too. This document applies to the use of ICP-MS for aqueous solution analysis.
The ultimate determination of the elements is described in a separate International Standard for each series of elements and matrix. The individual clauses of this document refer the user to these guidelines for the basic principles of the method and the configuration of the instrument.

  • Draft
    43 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
EN ISO 22435:2024(Main)
Gas cylinders - Cylinder valves with integrated pressure regulators - Specification and type testing (ISO 22435:2024)
kSIST FprEN ISO 22435:2024

This document specifies design, type test methods, marking and instruction requirements for cylinder valves with integrated pressure regulators (VIPRs) intended to be fitted to gas cylinders, pressure drums or tubes or used as a main valve for bundles of cylinders that convey compressed, liquefied or dissolved gases.
These are requirements for VIPRs that are in addition to those given in the relevant closure standard, for example, in ISO 10297 for cylinder valves, in ISO 17871 for quick-release cylinder valves, in ISO 17879 for self-closing cylinder valves or in ISO 23826 for ball valves. For ISO 17871, these requirements are only applicable to quick-release cylinder valves types B, C, D and E.
NOTE 1        If the pressure regulating system of a VIPR is acting as the primary valve operating mechanism, it is covered by the relevant closure standard, e.g. ISO 10297, ISO 17871, ISO 17879 and ISO 23826. This also includes designs where closure of the primary valve operating mechanism of a VIPR is obtained by closing the seat of the pressure regulating system.
NOTE 2        If the primary valve operating mechanism of a VIPR is located at the low-pressure side of the pressure regulating system, it is covered by the relevant closure standard, e.g. ISO 10297, ISO 17871, ISO 17879 and ISO 23826.
NOTE 3        The term “pressure receptacle” is used within this document to cover instances where no differentiation is necessary between gas cylinders, bundles of cylinders, pressure drums and tubes.
This document does not apply to VIPRs for
a)       medical applications (see ISO 10524-3);
b)       liquefied petroleum gas (LPG);
c)        cryogenic applications.
NOTE 4        Additional requirements for a VIPR with a residual pressure device (RPD) are specified in ISO 15996.
NOTE 5        Additional requirements for pressure relief valves can exist in international/regional regulations/ standards.

  • Draft
    39 pages
    English language
    sale 10% off
    e-Library read for
    1 day
CEN
EN 683-2:2024(Main)
Aluminium and aluminium alloys - Finstock - Part 2: Mechanical properties
kSIST FprEN 683-2:2024

This document specifies the mechanical properties of wrought aluminium and wrought aluminium alloy finstock.
The chemical composition limits of these materials are specified in EN 573 3, unless otherwise agreed between supplier and purchaser.
The designations of wrought aluminium and wrought aluminium alloys and the temper designations used in this document are specified in EN 573 3, and the temper designations are defined in EN 515.

  • Draft
    12 pages
    English language
    sale 10% off
    e-Library read for
    1 day