1、BS EN 1640:2009ICS 11.060.20NO COPYING WITHOUT BSI PERMISSION EXCEPT AS PERMITTED BY COPYRIGHT LAWBRITISH STANDARDDentistry Medicaldevices for dentistry EquipmentThis British Standardwas published underthe authority of theStandards Policy andStrategy Committee on 30November 2009 BSI 2009ISBN 978 0 5
2、80 63626 4Amendments/corrigenda issued since publicationDate CommentsBS EN 1640:2009National forewordThis British Standard is the UK implementation of EN 1640:2009. Itsupersedes BS EN 1640:2004 which is withdrawn.The UK participation in its preparation was entrusted to TechnicalCommittee CH/106/4, D
3、ental Instruments and Equipment.A list of organizations represented on this committee can be obtained onrequest to its secretary.This publication does not purport to include all the necessary provisionsof a contract. Users are responsible for its correct application.Compliance with a British Standar
4、d cannot confer immunityfrom legal obligations.BS EN 1640:2009EUROPEAN STANDARD NORME EUROPENNE EUROPISCHE NORM EN 1640 October 2009 ICS 11.060.20 Supersedes EN 1640:2004English Version Dentistry - Medical devices for dentistry - Equipment Art dentaire - Dispositifs mdicaux pour lart dentaire - Matr
5、iel Zahnheilkunde - Medizinprodukte fr die Zahnheilkunde - Ausrstung This European Standard was approved by CEN on 19 September 2009. 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 st
6、andard without any alteration. Up-to-date lists and bibliographical references concerning such national standards may be obtained on application to the CEN Management Centre or to any CEN member. This European Standard exists in three official versions (English, French, German). A version in any oth
7、er language made by translation under the responsibility of a CEN member into its own language and notified to the CEN Management Centre has the same status as the official versions. CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Cyprus, Czech Republic, Denmark, Estonia
8、, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland and United Kingdom. EUROPEAN COMMITTEE FOR STANDARDIZATION COMIT EUROPEN DE NORMALISATION EUROPIS
9、CHES KOMITEE FR NORMUNG Management Centre: Avenue Marnix 17, B-1000 Brussels 2009 CEN All rights of exploitation in any form and by any means reserved worldwide for CEN national Members. Ref. No. EN 1640:2009: EBS EN 1640:2009EN 1640:2009 (E) 2 Contents page Foreword 3Introduction . 41 Scope 52 Norm
10、ative references 53 Terms and definitions . 64 Requirements . 64.1 General 64.2 Chemical and physical properties . 64.2.1 Materials . 64.2.2 Contaminants and residues 74.2.3 Contact with substances 74.2.4 Ingress and leaking of substances 74.3 Control of contamination 74.4 Construction and environme
11、ntal properties . 74.5 Protection against radiation . 74.6 Equipment connected to or equipped with an energy source 84.7 Programmable electronic subsystems (software programmes) 84.8 Protection against electrical risks . 84.9 Protection against mechanical and thermal risks 84.9.1 Mechanical stabilit
12、y . 84.9.2 Vibration . 84.9.3 Noise . 84.9.4 Electricity, gas, hydraulic and pneumatic energy 84.9.5 Surface temperature 94.10 Controls and indicators 94.11 Clinical evaluation . 94.12 Marking, labelling and information supplied by the manufacturer 94.12.1 General 94.12.2 Symbols 94.12.3 Marking . 9
13、4.12.4 Label 104.12.5 Detachable components . 104.12.6 Instructions for use . 10Annex ZA (informative) Relationship between this European Standard and the Essential Requirements of EU Directive 93/42/EEC . 11Bibliography 12BS EN 1640:2009EN 1640:2009 (E) 3 Foreword This document (EN 1640:2009) has b
14、een prepared by Technical Committee CEN/TC 55 “Dentistry”, the secretariat of which is held by DIN. 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 April 2010, and conflicting national standards s
15、hall be withdrawn at the latest by April 2010. Attention is drawn to the possibility that some of the elements of this document may be the subject of patent rights. CEN and/or CENELEC shall not be held responsible for identifying any or all such patent rights. This document supersedes EN 1640:2004.
16、This document has been prepared under a mandate given to CEN by the European Commission and the European Free Trade Association, and supports essential requirements of EU Directive 93/42/EEC. For the relationship with EU Directive 93/42/EEC, see informative Annex ZA, which is an integral part of thi
17、s document. The following changes were made: a) Normative references: 1) Addition of new relevant product standards, issued after 2004: EN 60601-1-4, EN 62304, EN ISO 7494-1, EN ISO 10650-1, EN ISO 10650-2, EN ISO 14155-1, EN ISO 14155-2, EN ISO 14971, EN ISO 17664, EN ISO 21530; 2) Deletion of the
18、following withdrawn standard: EN ISO 7494. b) 4.11 Clinical evaluation: Clarification of requirement for a clinical evaluation; c) 4.12.6 Instructions for use: Clarification of requirement that information may be provided in an electronic format; d) Annex ZA: Actualisation of correspondence between
19、this European Standard and Directive 93/42/EEC, as amended by Directive 2007/47/EC. According to the CEN/CENELEC Internal Regulations, the national standards organizations of the following countries are bound to implement this European Standard: Austria, Belgium, Bulgaria, Cyprus, Czech Republic, De
20、nmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland and the United Kingdom. BS EN 1640:2009EN 1640:2009 (E) 4 Introduction There are th
21、ree levels of European Standards dealing with medical devices used in dentistry. These are as follows: Level 1: General requirements for medical devices; Level 2: Requirements for families of medical devices used in dentistry; Level 3: Specific requirements for types of medical devices used in denti
22、stry. There are no level 1 standards written exclusively in respect of medical devices used in dentistry. This European Standard is a level 2 standard and details requirements that apply to those items of dental equipment which are medical devices. For energy sources to be connected to dental instru
23、ments, this European Standard should be used in conjunction with EN 1639, which is applicable for dental instruments. This European Standard also indicates that there are additional requirements in the level 3 standards. Where available, these are included as normative references. To cover all the r
24、equirements for a particular product, it is necessary to use a standard of the lowest available level. In the Bibliography a reference for guidance on the classification of dental devices and accessories 3 is given. BS EN 1640:2009EN 1640:2009 (E) 5 1 Scope This European Standard specifies general r
25、equirements for dental equipment used in the practice of dentistry and which are medical devices. It includes requirements for intended performance, design attributes, components, packaging, marking, labelling, and information supplied by the manufacturer. This European Standard does not apply to de
26、ntal X-ray equipment. This European Standard does not apply to any dental instruments connected to an item of dental equipment. These instruments are covered by EN 1639. Tests for demonstrating compliance with this standard are contained in the level 3 standards, if appropriate. 2 Normative referenc
27、es The following referenced documents are indispensable for the application of this document. For dated references, only the edition cited applies. For undated references, the latest edition of the referenced document (including any amendments) applies. EN 980, Symbols for use in the labelling of me
28、dical devices EN 1041, Information supplied by the manufacturer of medical devices EN 1639, Dentistry Medical devices for dentistry Instruments EN 21942-1:1991, Dental vocabulary Part 1: General and clinical terms EN 21942-4:1993, Dental vocabulary Part 4: Dental equipment (ISO 1942-4:1989) EN 60601
29、-1, Medical electrical equipment Part 1: General requirements for basic safety and essential performance (IEC 60601-1:2005) EN 60601-2-22, Medical Electrical Equipment Part 2-22: Particular requirements for the safety of diagnostic and therapeutic laser equipment (IEC 60601-2-22:1995) EN 60601-1-4,
30、Medical electrical equipment Part 1: General requirements for safety 4. Collateral standard: Programmable electrical medical systems(IEC 60601-1-4:1996) EN 60825-1, Safety of laser products Part 1: Equipment classification and requirements (IEC 60825-1:2007) EN 62304. Medical device software Softwar
31、e life-cycle processes (IEC 62304:2006) EN ISO 6875, Dental equipment Dental patient chair (ISO 6875:1995) EN ISO 7488, Dental amalgamators (ISO 7488:1991) EN ISO 7494-1, Dentistry Dental units Part 1: General requirements and test methods (ISO 7494-1:2004) EN ISO 7494-2, Dentistry Dental units Part
32、 2: Water and air supply (ISO 7494-2:2003) EN ISO 9680, Dentistry Operating lights (ISO 9680:2007) EN ISO 9687, Dental equipment Graphical symbols (ISO 9687:1993) EN ISO 10637, Dental equipment High- and medium-volume suction systems (ISO 10637:1999) EN ISO 10650-1, Dentistry Powered polymerization
33、activators Part 1: Quartz tungsten halogen lamps (ISO 10650-1:2004) BS EN 1640:2009EN 1640:2009 (E) 6 EN ISO 10650-2, Dentistry Powered polymerization activators Part 2: Light-emitting diode (LED) lamps (ISO 10650-2:2007) EN ISO 11143, Dentistry Amalgam separators (ISO 11143:2008) EN ISO 11498, Dent
34、al handpieces Dental low-voltage electrical motors (ISO 11498:1997) EN ISO 13294, Dental handpieces Dental air-motors (ISO 13294:1997) EN ISO 14155-1, Clinical investigation of medical devices for human subjects Part 1: General requirements (ISO 14155-1:2003) EN ISO 14155-2, Clinical investigation o
35、f medical devices for human subjects Part 2: Clinical investigation plans (ISO 14155-2:2003) EN ISO 14971, Medical devices Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01) EN ISO 17664, Sterilization of medical devices Information to be provided by the
36、 manufacturer for the processing of resterilizable medical devices (ISO 17664:2004) EN ISO 21530, Dentistry Materials used for dental equipment surfaces Determination of resistance to chemical disinfectants (ISO 21530:2004) 3 Terms and definitions For the purposes of this European Standard, the term
37、s and definitions given in EN 21942-1:1991, EN 21942-4:1993 and the following apply. 3.1 dental equipment furniture, machines, apparatus and accessories thereto, specially made and/or presented for the use of authorized persons in the practice of dentistry and/or its associated procedures 4 Requirem
38、ents 4.1 General 4.1.1 Dental equipment shall comply with the requirements which are applicable to them bearing in mind the intended purpose of the equipment concerned. Conformity with these requirements shall be considered to be met by demonstrating compliance with the requirements of the following
39、 subclauses, if appropriate. 4.1.2 For those items of dental equipment intended to be used in connection with dental instruments, this standard and EN 1639 shall apply, if appropriate. 4.1.3 Dental equipment used in accordance with the instructions for use shall be safe for its intended purpose in t
40、he practice of dentistry. 4.1.4 Risk management shall be carried out and documented. This shall include a risk analysis in accordance with EN ISO 14971. 4.2 Chemical and physical properties 4.2.1 Materials Dental equipment shall comply with the material requirements as specified in the following pro
41、duct standards, if appropriate: EN ISO 6875, EN ISO 7494-1, EN ISO 7494-2, EN ISO 9680, EN ISO 10637, EN ISO 11143; EN ISO 21530. BS EN 1640:2009EN 1640:2009 (E) 7 NOTE Amalgam separators are considered to be medical devices only when incorporated as an integral part of the dental unit. 4.2.2 Contam
42、inants and residues Dental equipment shall be designed and manufactured so that the transfer of contaminants and residues does not compromise the clinical condition or the safety of patients, or the safety and health of users. Design specifications are given in the product standards. The following s
43、tandards shall apply, if appropriate: EN ISO 6875, EN ISO 7494-1, EN ISO 7494-2, EN ISO 10637, EN ISO 11143, EN ISO 11498, EN ISO 13294, EN ISO 21530. NOTE For plant area equipment further information is given in ISO/TS 22595-1 and 22595-2. 4.2.3 Contact with substances Dental equipment shall satisf
44、y the performance requirements for safe use with water, gases, oil, and other substances with which they enter into contact during normal use. The following standards shall apply, if appropriate: EN ISO 6875, EN ISO 7494-1, EN ISO 7494-2, EN ISO 9680, EN ISO 10637, EN ISO 11143, EN ISO 11498, EN ISO
45、 13294. 4.2.4 Ingress and leaking of substances Dental equipment shall be safe in regard to any risks due to ingress or leakage or both of water, gases, oil, and other substances during normal use. The following standards shall apply, if appropriate: EN 60601-1, EN ISO 6875, EN ISO 7488, EN ISO 7494
46、-1, EN ISO 7494-2, EN ISO 9680, EN ISO 10637, EN ISO 11143, EN ISO 21530. 4.3 Control of contamination Dental equipment shall be designed and manufactured so as to facilitate infection control. The following standards shall apply, if applicable: EN ISO 7494-1, EN ISO 7494-2, EN ISO 17664, EN ISO 215
47、30. 4.4 Construction and environmental properties 4.4.1 Dental equipment shall be designed and manufactured so that its physical and dimensional characteristics are suitable for its intended use and its use in combination according to the instructions for use. Connections to other devices shall be s
48、afe and create no risk due to physical features such as pressure or temperature or by accidental disconnection. The following standards shall apply, if appropriate: EN 60601-1, EN 60601-2-22, EN 60825-1, EN ISO 6875, EN ISO 7494-1, EN ISO 7494-2, EN ISO 9680, EN ISO 10637, EN ISO 10650-1, EN ISO 106
49、50-2, EN ISO 11143, EN ISO 11498, EN ISO 13294. 4.4.2 Dental equipment shall be designed and manufactured so that fire or explosion due to the use of any other substance shall be avoided. The following standards shall apply, if appropriate: EN ISO 6875, EN ISO 7494-1, EN ISO 9680, EN ISO 10637, EN ISO 11143. 4.5 Protection against radiation 4.5.1 Dental equipment emitting radi
