CEN TR 15133-2005 Nomenclature Collective terms and codes for groups of medical devices《术语 医用器械类集合名称和法典》.pdf
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1、PUBLISHED DOCUMENTPD CEN/TR 15133:2005Nomenclature Collective terms and codes for groups of medical devicesICS 01.040.11; 11.040.01g49g50g3g38g50g51g60g44g49g42g3g58g44g55g43g50g56g55g3g37g54g44g3g51g40g53g48g44g54g54g44g50g49g3g40g59g38g40g51g55g3g36g54g3g51g40g53g48g44g55g55g40g39g3g37g60g3g38g50g
2、51g60g53g44g42g43g55g3g47g36g58PD CEN/TR 15133:2005This Published Document was published under the authority of the Standards Policy and Strategy Committee on 12 December 2005 BSI 12 December 2005ISBN 0 580 46535 7National forewordThis Published Document is the official English language version of C
3、EN/TR 15133:2005.The UK participation in its preparation was entrusted by Technical Committee CH/210, Quality management and corresponding general aspects for medical devices, to Subcommittee CH/210/3, General terminology and symbols, which has the responsibility to: aid enquirers to understand the
4、text; present to the responsible international/European committee any enquiries on the interpretation, or proposals for change, and keep UK interests informed; monitor related international and European developments and promulgate them in the UK.A list of organizations represented on this committee
5、can be obtained on request to its secretary.Cross-referencesThe British Standards which implement international or European publications referred to in this document may be found in the BSI Catalogue under the section entitled “International Standards Correspondence Index”, or by using the “Search”
6、facility of the BSI Electronic Catalogue or of British Standards Online.This publication does not purport to include all the necessary provisions of a contract. Users are responsible for its correct application.Compliance with a Published Document does not of itself confer immunity from legal obliga
7、tions.Summary of pagesThis document comprises a front cover, an inside front cover, the CEN/TR title page, pages 2 to 15 and a back cover.The BSI copyright notice displayed in this document indicates when the document was last issued.Amendments issued since publicationAmd. No. Date CommentsTECHNICAL
8、 REPORTRAPPORT TECHNIQUETECHNISCHER BERICHTCEN/TR 15133June 2005ICS 01.040.11; 11.040.01English versionNomenclature - Collective terms and codes for groups ofmedical devicesNomenclature - Termes et codes collectifs pour lesgroupes de dispositifs mdicauxNomenklatur - Sammelbegriffe und Kodes fr Grupp
9、en vonMedizinproduktenThis Technical Report was approved by CEN on 6 May 2005. It has been drawn up by the Technical Committee CEN/TC 257.CEN members are the national standards bodies of Austria, Belgium, Cyprus, Czech Republic, Denmark, Estonia, Finland, France,Germany, Greece, Hungary, Iceland, Ir
10、eland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Slovakia,Slovenia, Spain, Sweden, Switzerland and United Kingdom.EUROPEAN COMMITTEE FOR STANDARDIZATIONCOMIT EUROPEN DE NORMALISATIONEUROPISCHES KOMITEE FR NORMUNGManagement Centre: rue de Stassart, 36 B-1050
11、Brussels 2005 CEN All rights of exploitation in any form and by any means reservedworldwide for CEN national Members.Ref. No. CEN/TR 15133:2005: E2 Contents Page Foreword 3 Introduction4 1 Scope .5 2 Lists of collective terms .5 2.1 Application of Common Technology.5 2.2 Using similar manufacturing
12、procedures .11 2.3 For similar medical procedures .12 2.4 Using common materials13 2.5 Specific risk-associated considerations .14 Bibliography.15 CEN/TR 15133:20053 Foreword This document (CEN/TR 15133:2005) has been prepared by Technical Committee CEN/TC 257 “Symbols and information provided with
13、medical devices and nomenclature for regulatory data exchange”, the secretariat of which is held by SFS. This CEN report has been prepared under the mandate (M321) given to CEN by the European Commission and the European Free Trade Association. This CEN Report is intended to complement the specific
14、requirements of the EU regulations on medical devices relating to information exchanged between parties communicating in conformity with requirements of the Directives. According to the CEN/CENELEC Internal Regulations, the national standards organizations of the following countries are bound to ann
15、ounce this CEN Technical Report: 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 King
16、dom. CEN/TR 15133:20054 Introduction This Technical Report contains collective terms for those medical devices which share common features and are identified in the Global Medical device Nomenclature (GMDN), published as CR 14230:2001 Global medical device nomenclature for the purpose of regulatory
17、data exchange (identical to ISO/TS 20225:2001 Whereas the GMDN is designed and was developed for regulatory data exchange in areas such as vigilance reporting and tracking of medical device safety, there is a need for a set of terms that are more refined than the GMDN category terms, yet broader tha
18、n the GMDN generic device group terms, to be used in the application of the medical device directives where the use of collective terms provides adequate identification. These collective terms are intended to be used for example: to illustrate the scope of certificates issued by Notified Bodies when
19、 assessing which groups, families or types of medical devices are covered within a manufacturers quality system, to be used to identify the range of skills and general technological abilities for which a Notified Body has been approved, and is so appointed by the relevant Competent Authority, for th
20、e exchanges of information between Competent Authorities when general information on individual manufacturers capabilities is notified for inclusion in the European Database for Medical Devices (EUDAMED). These terms, named “collective terms“, are appropriate for providing general groupings to meet,
21、 in particular, the above identified requirements. In the preparation of this CEN REPORT a number of principles were identified which were used in grouping together generic device group terms of the GMDN within the proposed “collective terms”. These were: Devices covered by the application of common
22、 technology Devices manufactured using similar manufacturing procedures, and with common technical features. Devices manufactured for the application of similar Medical Procedures Devices manufactured using common materials requiring special skills. Devices developed to meet specific risk-associated
23、 considerations. For ease of electronic transmission of data, and to eliminate the possibility of confusion with other coding systems having a three-digit code used for information concerning Medical Devices, each collective term is assigned a three-digit random code with the prefix “CT” (Collective
24、 Term), which identifies the code source. It is expected that as the collective terms are brought into use, they will be assigned to the generic device group terms of the GMDN. The Maintenance Agency (MA) of the GMDN will make these links available. Details of progress in this area will be posted on
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