Commission Implementing Decision (EU) 2020/437 of 24 March 2020 on the harmonised standards for medical devices drafted in support of Council Directive 93/42/EEC
Date: 2020-03-24
Institutions: Directorate-General for Health and Food Safety, European Commission
Subjects: Cenelec, European Committee for Standardisation, European standard, harmonisation of standards, medical device








LI2020090EN.01000101.xml










25.3.2020   


EN


Official Journal of the European Union


LI 90/1








            COMMISSION IMPLEMENTING DECISION (EU) 2020/437
of 24 March 2020
         
on the harmonised standards for medical devices drafted in support of Council Directive 93/42/EEC


THE EUROPEAN COMMISSION,

Having regard to the Treaty on the Functioning of the European Union,


Having regard to Regulation (EU) No 1025/2012 of the European Parliament and of the Council of 25 October 2012 on European standardisation, amending Council Directives 89/686/EEC and 93/15/EEC and Directives 94/9/EC, 94/25/EC, 95/16/EC, 97/23/EC, 98/34/EC, 2004/22/EC, 2007/23/EC, 2009/23/EC and 2009/105/EC of the European Parliament and of the Council and repealing Council Decision 87/95/EEC and Decision No 1673/2006/EC of the European Parliament and of the Council (1), and in particular Article 10(6) thereof,

Whereas:







(1)


In accordance with Article 5(1) of Council Directive 93/42/EEC (2), Member States are to presume compliance with the essential requirements referred to in Article 3 of that Directive in respect of medical devices which are in conformity with the relevant national standards adopted pursuant to the harmonized standards the references of which have been published in the Official Journal of the European Union.












(2)


By letters BC/CEN/CENELEC/09/89 of 19 December 1991, M/023 - BC/CEN/03/023/93-08 of 5 August 1993 and M/295 of 9 September 1999, the Commission made requests to the European Committee for Standardisation (CEN) and the European Committee for Electrotechnical Standardisation (Cenelec) for the drafting of new harmonised standards and the revision of existing harmonised standards in support of Directive 93/42/EEC.












(3)


On the basis of the request M/295 of 9 September 1999, CEN revised the harmonised standards EN ISO 10993-11:2009, EN 14683:2005 and EN ISO 15747:2011, the references of which have been published in the Official Journal of the European Union (3), in order to include the latest technical and scientific progress. This resulted in the adoption of the harmonised standards EN ISO 10993-11:2018, EN 14683:2019+AC:2019 and EN ISO 15747:2019.












(4)


The Commission together with CEN has assessed whether standards EN ISO 10993-11:2018, EN 14683:2019+AC:2019 and EN ISO 15747:2019 comply with the request.












(5)


The harmonised standards EN ISO 10993-11:2018, EN 14683:2019+AC:2019 and EN ISO 15747:2019 satisfy the requirements which they aim to cover and which are set out in Directive 93/42/EEC. It is therefore appropriate to publish the references of those standards in the Official Journal of the European Union.












(6)


The harmonised standards EN ISO 10993-11:2018, EN 14683:2019+AC:2019 and EN ISO 15747:2019 replace the harmonised standards EN ISO 10993-11:2009, EN 14683:2005 and EN ISO 15747:2011 respectively. It is therefore necessary to withdraw the references of standards EN ISO 10993-11:2009, EN 14683:2005 and EN ISO 15747:2011 from the Official Journal of the European Union.












(7)


On the basis of the request BC/CEN/CENELEC/09/89 of 19 December 1991, CEN revised the harmonised standards EN ISO 11137-1:2015, EN ISO 13408-2:2011 and EN ISO 13485:2016, the references of which have been published in the Official Journal of the European Union (4), in order to include the latest technical and scientific progress. This resulted in the adoption of the harmonised standards EN ISO 11137-1:2015/A2:2019 and EN ISO 13408-2:2018 and the corrigendum EN ISO 13485:2016/AC:2018.












(8)


The Commission together with CEN has assessed whether standards EN ISO 11137-1:2015/A2:2019 and EN ISO 13408-2:2018 and the corrigendum EN ISO 13485:2016/AC:2018 comply with the request.












(9)


The harmonised standards EN ISO 11137-1:2015/A2:2019 and EN ISO 13408-2:2018 and the corrigendum EN ISO 13485:2016/AC:2018 satisfy the requirements which they aim to cover and which are set out in Directive 93/42/EEC. It is therefore appropriate to publish the references of those standards and of the corrigendum in the Official Journal of the European Union.












(10)


The harmonised standard EN ISO 13408-2:2018 and the corrigendum EN ISO 13485:2016/AC:2018 replace the harmonised standard EN ISO 13408-2:2011 and the corrigendum EN ISO 13485:2016/AC:2016 respectively. It is therefore necessary to withdraw the reference of standard EN ISO 13408-2:2011 and of corrigendum EN ISO 13485:2016/AC:2016 from the Official Journal of the European Union.












(11)


On the basis of the request M/023 - BC/CEN/03/023/93-08 of 5 August 1993, CEN revised the harmonised standards EN ISO 11990-1:2004, EN ISO 11990-2:2004, EN 13976-2:2011, EN ISO 15883-4:2009, EN ISO 17664:2004 and EN ISO 21987:2009, the references of which have been published in the Official Journal of the European Union (5), in order to include the latest technical and scientific progress. This resulted in the adoption of the harmonised standards EN ISO 11990:2018, EN 13976-2:2018, EN ISO 15883-4:2018, EN ISO 17664:2017 and EN ISO 21987:2017.












(12)


The Commission together with CEN has assessed whether standards EN ISO 11990:2018, EN 13976-2:2018, EN ISO 15883-4:2018, EN ISO 17664:2017 and EN ISO 21987:2017 comply with the request.












(13)


The harmonised standards EN ISO 11990:2018, EN 13976-2:2018, EN ISO 15883-4:2018, EN ISO 17664:2017 and EN ISO 21987:2017 satisfy the requirements which they aim to cover and which are set out in Directive 93/42/EEC. It is therefore appropriate to publish the references of those standards in the Official Journal of the European Union.












(14)


The harmonised standards EN ISO 11990:2018, EN 13976-2:2018, EN ISO 15883-4:2018, EN ISO 17664:2017 and EN ISO 21987:2017 replace the harmonised standards EN ISO 11990-1:2004, EN ISO 11990-2:2004, EN 13976-2:2011, EN ISO 15883-4:2009, EN ISO 17664:2004 and EN ISO 21987:2009 respectively. It is therefore necessary to withdraw the references of standards EN ISO 11990-1:2004, EN ISO 11990-2:2004, EN 13976-2:2011, EN ISO 15883-4:2009, EN ISO 17664:2004 and EN ISO 21987:2009 from the Official Journal of the European Union.












(15)


On the basis of the request M/295 of 9 September 1999, CEN drafted the new harmonised standards EN 11608-7:2017, EN 13795-1:2019, EN 13795-2:2019 and EN ISO 81060-2:2019. The Commission together with CEN has assessed whether those standards comply with the request.












(16)


The harmonised standards EN 11608-7:2017, EN 13795-1:2019, EN 13795-2:2019 and EN ISO 81060-2:2019 satisfy the requirements which they aim to cover and which are set out in Directive 93/42/EEC. It is therefore appropriate to publish the references of those standards in the Official Journal of the European Union.












(17)


On the basis of the request BC/CEN/CENELEC/09/89 of 19 December 1991, CEN drafted the new harmonised standard EN ISO 25424:2019. The Commission together with CEN has assessed whether that standard complies with the request.












(18)


The harmonised standard EN ISO 25424:2019 satisfies the requirements, which it aims to cover and which are set out in Directive 93/42/EEC. It is therefore appropriate to publish the reference of that standard in the Official Journal of the European Union.












(19)


In order to give manufacturers sufficient time to adapt their products to the revised specifications in standards and the corrigendum published by this Decision, it is necessary to defer the withdrawal of the reference of the standards and the corrigendum that are replaced.












(20)


In the interests of clarity and legal certainty, a complete list of references of harmonised standards drafted in support of Directive 93/42/EEC and satisfying the essential requirements they aim to cover should be published in one act. The other references of standards published in the Commission communication 2017/C 389/03 (6) should therefore also be included in this Decision. That Communication should therefore be repealed from the date of entry into force of this Decision. However, it should continue to apply in respect of the references of the standards that are withdrawn by this Decision, given that it is necessary to defer withdrawal of those references.












(21)


In accordance with the second subparagraph of Article 120(2) of Regulation (EU) 2017/745 of the European Parliament and of the Council (7), certificates issued by notified bodies in accordance with Directive 93/42/EEC from 25 May 2017 are to remain valid until the end of the period indicated on the certificate, which is not to exceed five years from its issuance. They are to however become void at the latest on 27 May 2024. In accordance with the first subparagraph of Article 120(3) of Regulation (EU) 2017/745 a device which is a class I device pursuant to Directive 93/42/EEC, for which the declaration of conformity was drawn up prior to 26 May 2020 and for which the conformity assessment procedure pursuant to this Regulation requires the involvement of a notified body, or which has a certificate that was issued in accordance with Directive 93/42/EEC and that is valid by virtue of Article 120(2), may be placed on the market or put into service until 26 May 2024, provided that from 26 May 2020 it continues to comply with Directive 93/42/EEC, and provided there are no significant changes in the design and intended purpose. This Decision should therefore apply only until 26 May 2024.












(22)


The requirements for medical devices laid down in Directive 93/42/EEC are different from those laid down in Regulation (EU) 2017/745. The standards drafted in support of Directive 93/42/EEC should therefore not be used to demonstrate conformity with requirements of Regulation (EU) 2017/745.












(23)


Compliance with a harmonised standard confers a presumption of conformity with the corresponding essential requirements set out in Union harmonisation legislation from the date of publication of the reference of such standard in the Official Journal of the European Union. This Decision should therefore enter into force on the date of its publication,





HAS ADOPTED THIS DECISION:



Article 1
The references of the harmonised standards for medical devices drafted in support of Directive 93/42/EEC and listed in Annex I to this Decision are hereby published in the Official Journal of the European Union.


Article 2
Commission communication 2017/C 389/03 is repealed. It shall continue to apply until 30 September 2021 in respect of the references of the standards listed in Annex II to this Decision.


Article 3
The harmonised standards for medical devices drafted in support of Directive 93/42/EEC and listed in Annexes I and II to this Decision may not be used to confer presumption of conformity with the requirements of Regulation (EU) 2017/745.


Article 4
This Decision shall enter into force on the day of its publication in the Official Journal of the European Union.
It shall apply until 26 May 2024.




Done at Brussels, 24 March 2020.


For the Commission


The President

Ursula VON DER LEYEN
            





(1)  
            OJ L 316, 14.11.2012, p. 12.

(2)  Council Directive 93/42/EEC of 14 June 1993 concerning medical devices (OJ L 169, 12.7.1993, p. 1).

(3)  
            OJ C 389, 17.11.2017, p. 29.

(4)  
            OJ C 389, 17.11.2017, p. 29.

(5)  
            OJ C 389, 17.11.2017, p. 29.

(6)  Commission communication in the framework of the implementation of Council Directive 93/42/EEC concerning medical devices (2017/C 389/03) (OJ C 389, 17.11.2017, p. 29).

(7)  Regulation (EU) 2017/745 of the European Parliament and of the Council of 5 April 2017 on medical devices, amending Directive 2001/83/EC, Regulation (EC) No 178/2002 and Regulation (EC) No 1223/2009 and repealing Council Directives 90/385/EEC and 93/42/EEC (OJ L 117, 5.5.2017, p. 1).




ANNEX I






No


Reference of the standard




1.


EN 285:2006+A2:2009
Sterilization - Steam sterilizers - Large sterilizers




2.


EN 455-1:2000
Medical gloves for single use - Part 1: Requirements and testing for freedom from holes




3.


EN 455-2:2009+A2:2013
Medical gloves for single use - Part 2: Requirements and testing for physical properties




4.


EN 455-3:2006
Medical gloves for single use - Part 3: Requirements and testing for biological evaluation




5.


EN 455-4:2009
Medical gloves for single use - Part 4: Requirements and testing for shelf life determination




6.


EN 556-1:2001
Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices
EN 556-1:2001/AC:2006




7.


EN 556-2:2015
Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices




8.


EN 794-3:1998+A2:2009
Lung ventilators - Part 3: Particular requirements for emergency and transport ventilators




9.


EN 1041:2008
Information supplied by the manufacturer of medical devices




10.


EN 1060-3:1997+A2:2009
Non-invasive sphygmomanometers - Part 3: Supplementary requirements for electro-mechanical blood pressure measuring systems




11.


EN 1060-4:2004
Non-invasive sphygmomanometers - Part 4: Test procedures to determine the overall system accuracy of automated non-invasive sphygmomanometers




12.


EN ISO 1135-4:2011
Transfusion equipment for medical use - Part 4: Transfusion sets for single use (ISO 1135-4:2010)




13.


EN 1282-2:2005+A1:2009
Tracheostomy tubes - Part 2: Paediatric tubes (ISO 5366-3:2001, modified)




14.


EN 1422:1997+A1:2009
Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods




15.


EN 1618:1997
Catheters other than intravascular catheters - Test methods for common properties




16.


EN 1639:2009
Dentistry - Medical devices for dentistry - Instruments




17.


EN 1640:2009
Dentistry - Medical devices for dentistry - Equipment




18.


EN 1641:2009
Dentistry - Medical devices for dentistry - Materials




19.


EN 1642:2011
Dentistry - Medical devices for dentistry - Dental implants




20.


EN 1707:1996
Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment - Lock fittings




21.


EN 1782:1998+A1:2009
Tracheal tubes and connectors




22.


EN 1789:2007+A1:2010
Medical vehicles and their equipment - Road ambulances




23.


EN 1820:2005+A1:2009
Anaesthetic reservoir bags (ISO 5362:2000, modified)




24.


EN 1865-1:2010+A1:2015
Patient handling equipment used in road ambulances - Part 1: General stretcher systems and patient handling equipment




25.


EN 1865-2:2010+A1:2015
Patient handling equipment used in road ambulances - Part 2: Power assisted stretcher




26.


EN 1865-3:2012
Patient handling equipment used in road ambulances - Part 3: Heavy duty stretcher




27.


EN 1865-4:2012
Patient handling equipment used in road ambulances - Part 4: Foldable patient transfer chair




28.


EN 1865-5:2012
Patient handling equipment used in road ambulances - Part 5: Stretcher support




29.


EN 1985:1998
Walking aids - General requirements and test methods
Notice: This standard still needs to be amended to take into account the requirements introduced by Directive 2007/47/EC. The amended standard will be published by CEN as soon as possible. Manufacturers are advised to check whether all relevant essential requirements of the amended directive are appropriately covered.




30.


EN ISO 3826-2:2008
Plastics collapsible containers for human blood and blood components - Part 2: Graphical symbols for use on labels and instruction leaflets (ISO 3826-2:2008)




31.


EN ISO 3826-3:2007
Plastics collapsible containers for human blood and blood components - Part 3: Blood bag systems with integrated features (ISO 3826- 3:2006)




32.


EN ISO 3826-4:2015
Plastics collapsible containers for human blood and blood components - Part 4: Aphaeresis blood bag systems with integrated features (ISO 3826-4:2015)




33.


EN ISO 4074:2002
Natural latex rubber condoms - Requirements and test methods (ISO 4074:2002)




34.


EN ISO 4135:2001
Anaesthetic and respiratory equipment - Vocabulary (ISO 4135:2001)




35.


EN ISO 5359:2008
Low-pressure hose assemblies for use with medical gases (ISO 5359:2008)
EN ISO 5359:2008/A1:2011




36.


EN ISO 5360:2009
Anaesthetic vaporizers - Agent-specific filling systems (ISO 5360:2006)




37.


EN ISO 5366-1:2009
Anaesthetic and respiratory equipment - Tracheostomy tubes - Part 1: Tubes and connectors for use in adults (ISO 5366-1:2000)




38.


EN ISO 5840:2009
Cardiovascular implants - Cardiac valve prostheses (ISO 5840:2005)




39.


EN ISO 7197:2009
Neurosurgical implants - Sterile, single-use hydrocephalus shunts and components (ISO 7197:2006, including Cor 1:2007)




40.


EN ISO 7376:2009
Anaesthetic and respiratory equipment - Laryngoscopes for tracheal intubation (ISO 7376:2009)




41.


EN ISO 7396-1:2007
Medical gas pipeline systems - Part 1: Pipeline systems for compressed medical gases and vacuum (ISO 7396-1:2007)
EN ISO 7396-1:2007/A1:2010
EN ISO 7396-1:2007/A2:2010




42.


EN ISO 7396-2:2007
Medical gas pipeline systems - Part 2: Anaesthetic gas scavenging disposal systems (ISO 7396-2:2007)




43.


EN ISO 7886-3:2009
Sterile hypodermic syringes for single use - Part 3: Auto-disable syringes for fixed-dose immunization (ISO 7886-3:2005)




44.


EN ISO 7886-4:2009
Sterile hypodermic syringes for single use - Part 4: Syringes with reuse prevention feature (ISO 7886-4:2006)




45.


EN ISO 8185:2009
Respiratory tract humidifiers for medical use - Particular requirements for respiratory humidification systems (ISO 8185:2007)




46.


EN ISO 8359:2009
Oxygen concentrators for medical use - Safety requirements (ISO 8359:1996)
EN ISO 8359:2009/A1:2012




47.


EN ISO 8835-2:2009
Inhalational anaesthesia systems - Part 2: Anaesthetic breathing systems (ISO 8835- 2:2007)




48.


EN ISO 8835-3:2009
Inhalational anaesthesia systems - Part 3: Transfer and receiving systems of active anaesthetic gas scavenging systems (ISO 8835-3:2007)
EN ISO 8835-3:2009/A1:2010




49.


EN ISO 8835-4:2009
Inhalational anaesthesia systems - Part 4: Anaesthetic vapour delivery devices (ISO 8835- 4:2004)




50.


EN ISO 8835-5:2009
Inhalational anaesthesia systems - Part 5: Anaesthetic ventilators (ISO 8835-5:2004)




51.


EN ISO 9170-1:2008
Terminal units for medical gas pipeline systems - Part 1: Terminal units for use with compressed medical gases and vacuum (ISO 9170-1:2008)




52.


EN ISO 9170-2:2008
Terminal units for medical gas pipeline systems - Part 2: Terminal units for anaesthetic gas scavenging systems (ISO 9170-2:2008)




53.


EN ISO 9360-1:2009
Anaesthetic and respiratory equipment - Heat and moisture exchangers (HMEs) for humidifying respired gases in humans - Part 1: HMEs for use with minimum tidal volumes of 250 ml (ISO 9360-1:2000)




54.


EN ISO 9360-2:2009
Anaesthetic and respiratory equipment - Heat and moisture exchangers (HMEs) for humidifying respired gases in humans - Part 2: HMEs for use with tracheostomized patients having minimum tidal volumes of 250 ml (ISO 9360-2:2001)




55.


EN ISO 9713:2009
Neurosurgical implants - Self-closing intracranial aneurysm clips (ISO 9713:2002)




56.


EN ISO 10079-1:2009
Medical suction equipment - Part 1: Electrically powered suction equipment - Safety requirements (ISO 10079-1:1999)




57.


EN ISO 10079-2:2009
Medical suction equipment - Part 2: Manually powered suction equipment (ISO 10079-2:1999)




58.


EN ISO 10079-3:2009
Medical suction equipment - Part 3: Suction equipment powered from a vacuum or pressure source (ISO 10079-3:1999)




59.


EN ISO 10328:2016
Prosthetics - Structural testing of lower-limb prostheses - Requirements and test methods (ISO 10328:2016)




60.


EN ISO 10524-1:2006
Pressure regulators for use with medical gases - Part 1: Pressure regulators and pressure regulators with flow-metering devices (ISO 10524- 1:2006)




61.


EN ISO 10524-2:2006
Pressure regulators for use with medical gases - Part 2: Manifold and line pressure regulators (ISO 10524-2:2005)




62.


EN ISO 10524-3:2006
Pressure regulators for use with medical gases - Part 3: Pressure regulators integrated with cylinder valves (ISO 10524-3:2005)




63.


EN ISO 10524-4:2008
Pressure regulators for use with medical gases - Part 4: Low-pressure regulators (ISO 10524- 4:2008)




64.


EN ISO 10535:2006
Hoists for the transfer of disabled persons - Requirements and test methods (ISO 10535:2006)
Notice: This standard still needs to be amended to take into account the requirements introduced by Directive 2007/47/EC. The amended standard will be published by CEN as soon as possible. Manufacturers are advised to check whether all relevant essential requirements of the amended directive are appropriately covered.




65.


EN ISO 10555-1:2009
Sterile, single-use intravascular catheters - Part 1: General requirements (ISO 10555-1:1995, including Amd 1:1999 and Amd 2:2004)




66.


EN ISO 10651-2:2009
Lung ventilators for medical use - Particular requirements for basic safety and essential performance - Part 2: Home care ventilators for ventilator-dependent patients (ISO 10651- 2:2004)




67.


EN ISO 10651-4:2009
Lung ventilators - Part 4: Particular requirements for operator-powered resuscitators (ISO 10651-4:2002)




68.


EN ISO 10651-6:2009
Lung ventilators for medical use - Particular requirements for basic safety and essential performance - Part 6: Home-care ventilatory support devices (ISO 10651-6:2004)




69.


EN ISO 10993-1:2009
Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2009)
EN ISO 10993-1:2009/AC:2010




70.


EN ISO 10993-3:2014
Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2014)




71.


EN ISO 10993-4:2009
Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002, including Amd 1:2006)




72.


EN ISO 10993-5:2009
Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)




73.


EN ISO 10993-6:2009
Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007)




74.


EN ISO 10993-7:2008
Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008)
EN ISO 10993-7:2008/AC:2009




75.


EN ISO 10993-9:2009
Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2009)




76.


EN ISO 10993-11:2018
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2017)




77.


EN ISO 10993-12:2012
Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012)




78.


EN ISO 10993-13:2010
Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010)




79.


EN ISO 10993-14:2009
Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)




80.


EN ISO 10993-15:2009
Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000)




81.


EN ISO 10993-16:2010
Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2010)




82.


EN ISO 10993-17:2009
Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)




83.


EN ISO 10993-18:2009
Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005)




84.


EN ISO 11135-1:2007
Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11135-1:2007)




85.


EN ISO 11137-1:2015
Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006, including Amd 1:2013)
EN ISO 11137-1:2015/A2:2019




86.


EN ISO 11137-2:2015
Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2013)




87.


EN ISO 11138-2:2009
Sterilization of health care products - Biological indicators - Part 2: Biological indicators for ethylene oxide sterilization processes (ISO 11138-2:2006)




88.


EN ISO 11138-3:2009
Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes (ISO 11138-3:2006)




89.


EN ISO 11140-1:2009
Sterilization of health care products - Chemical indicators - Part 1: General requirements (ISO 11140-1:2005)




90.


EN ISO 11140-3:2009
Sterilization of health care products - Chemical indicators - Part 3: Class 2 indicator systems for use in the Bowie and Dick-type steam penetration test (ISO 11140-3:2007, including Cor 1:2007)




91.


EN ISO 11197:2009
Medical supply units (ISO 11197:2004)




92.


EN ISO 11607-1:2009
Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2006)




93.


EN ISO 11607-2:2006
Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006)




94.


EN ISO 11608-7:2017
Needle-based injection systems for medical use - Requirements and test methods - Part 7: Accessibility for persons with visual impairment (ISO 11608-7:2016)




95.


EN ISO 11737-1:2006
Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms on products (ISO 11737-1:2006)
EN ISO 11737-1:2006/AC:2009




96.


EN ISO 11737-2:2009
Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO 11737-2:2009)




97.


EN ISO 11810-1:2009
Lasers and laser-related equipment - Test method and classification for the laser resistance of surgical drapes and/or patient protective covers - Part 1: Primary ignition and penetration (ISO 11810-1:2005)




98.


EN ISO 11810-2:2009
Lasers and laser-related equipment - Test method and classification for the laser-resistance of surgical drapes and/or patient-protective covers - Part 2: Secondary ignition (ISO 11810-2:2007)




99.


EN ISO 11979-8:2009
Ophthalmic implants - Intraocular lenses - Part 8: Fundamental requirements (ISO 11979- 8:2006)




100.


EN ISO 11990:2018
Lasers and laser-related equipment - Determination of laser resistance of tracheal tube shaft and tracheal cuffs (ISO 11990:2018)




101.


EN 12006-2:1998+A1:2009
Non active surgical implants - Particular requirements for cardiac and vascular implants - Part 2: Vascular prostheses including cardiac valve conduits




102.


EN 12006-3:1998+A1:2009
Non active surgical implants - Particular requirements for cardiac and vascular implants - Part 3: Endovascular devices




103.


EN 12183:2009
Manual wheelchairs - Requirements and test methods




104.


EN 12184:2009
Electrically powered wheelchairs, scooters and their chargers - Requirements and test methods




105.


EN 12342:1998+A1:2009
Breathing tubes intended for use with anaesthetic apparatus and ventilators




106.


EN 12470-1:2000+A1:2009
Clinical thermometers - Part 1: Metallic liquid- in-glass thermometers with maximum device




107.


EN 12470-2:2000+A1:2009
Clinical thermometers - Part 2: Phase change type (dot matrix) thermometers




108.


EN 12470-3:2000+A1:2009
Clinical thermometers - Part 3: Performance of compact electrical thermometers (non-predictive and predictive) with maximum device




109.


EN 12470-4:2000+A1:2009
Clinical thermometers - Part 4: Performance of electrical thermometers for continuous measurement




110.


EN 12470-5:2003
Clinical thermometers - Part 5: Performance of infra-red ear thermometers (with maximum device)
Notice: This standard still needs to be amended to take into account the requirements introduced by Directive 2007/47/EC. The amended standard will be published by CEN as soon as possible. Manufacturers are advised to check whether all relevant essential requirements of the amended directive are appropriately covered.




111.


EN ISO 12870:2009
Ophthalmic optics - Spectacle frames - Requirements and test methods (ISO 12870:2004)




112.


EN 13060:2014
Small steam sterilizers




113.


EN ISO 13408-1:2015
Aseptic processing of health care products - Part 1: General requirements (ISO 13408-1:2008, including Amd 1:2013)




114.


EN ISO 13408-2:2018
Aseptic processing of health care products - Part 2: Sterilizing filtration (ISO 13408-2:2018)




115.


EN ISO 13408-3:2011
Aseptic processing of health care products - Part 3: Lyophilization (ISO 13408-3:2006)




116.


EN ISO 13408-4:2011
Aseptic processing of health care products - Part 4: Clean-in-place technologies (ISO 13408-4:2005)




117.


EN ISO 13408-5:2011
Aseptic processing of health care products - Part 5: Sterilization in place (ISO 13408-5:2006)




118.


EN ISO 13408-6:2011
Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005)




119.


EN ISO 13408-7:2015
Aseptic processing of health care products - Part 7: Alternative processes for medical devices and combination products (ISO 13408-7:2012)




120.


EN ISO 13485:2016
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
EN ISO 13485:2016/AC:2018




121.


EN 13544-1:2007+A1:2009
Respiratory therapy equipment - Part 1: Nebulizing systems and their component




122.


EN 13544-2:2002+A1:2009
Respiratory therapy equipment - Part 2: Tubing and connectors




123.


EN 13544-3:2001+A1:2009
Respiratory therapy equipment - Part 3: Air entrainment devices




124.


EN 13624:2003
Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal activity of chemical disinfectants for instruments used in the medical area - Test method and requirements (phase 2, step 1)




125.


EN 13718-1:2008
Medical vehicles and their equipment - Air ambulances - Part 1: Requirements for medical devices used in air ambulances




126.


EN 13718-2:2015
Medical vehicles and their equipment - Air ambulances - Part 2: Operational and technical requirements for air ambulances




127.


EN 13726-1:2002
Test methods for primary wound dressings - Part 1: Aspects of absorbency
EN 13726-1:2002/AC:2003




128.


EN 13726-2:2002
Test methods for primary wound dressings - Part 2: Moisture vapour transmission rate of permeable film dressings




129.


EN 13727:2012
Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity in the medical area - Test method and requirements (phase 2, step 1)




130.


EN 13795-1:2019
Surgical clothing and drapes - Requirements and test methods - Part 1: Surgical drapes and gowns




131.


EN 13795-2:2019
Surgical clothing and drapes - Requirements and test methods - Part 2: Clean air suits




132.


EN 13867:2002+A1:2009
Concentrates for haemodialysis and related therapies




133.


EN 13976-1:2011
Rescue systems - Transportation of incubators - Part 1: Interface conditions




134.


EN 13976-2:2018
Rescue systems - Transportation of incubators - Part 2: System requirements




135.


EN 14079:2003
Non-active medical devices - Performance requirements and test methods for absorbent cotton gauze and absorbent cotton and viscose gauze




136.


EN 14139:2010
Ophthalmic optics - Specifications for ready-to- wear spectacles




137.


EN ISO 14155:2011
Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)
EN ISO 14155:2011/AC:2011




138.


EN 14180:2003+A2:2009
Sterilizers for medical purposes - Low temperature steam and formaldehyde sterilizers - Requirements and testing




139.


EN 14348:2005
Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of mycobactericidal activity of chemical disinfectants in the medical area including instrument disinfectants - Test methods and requirements (phase 2, step 1)




140.


EN ISO 14408:2009
Tracheal tubes designed for laser surgery - Requirements for marking and accompanying information (ISO 14408:2005)




141.


EN 14561:2006
Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of bactericidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)




142.


EN 14562:2006
Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of fungicidal or yeasticidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)




143.


EN 14563:2008
Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of mycobactericidal or tuberculocidal activity of chemical disinfectants used for instruments in the medical area - Test method and requirements (phase 2, step 2)




144.


EN ISO 14602:2011
Non-active surgical implants - Implants for osteosynthesis - Particular requirements (ISO 14602:2010)




145.


EN ISO 14607:2009
Non-active surgical implants - Mammary implants - Particular requirements (ISO 14607:2007)




146.


EN ISO 14630:2009
Non-active surgical implants - General requirements (ISO 14630:2008)




147.


EN 14683:2019+AC:2019
Medical face masks - Requirements and test methods




148.


EN ISO 14889:2009
Ophthalmic optics - Spectacle lenses - Fundamental requirements for uncut finished lenses (ISO 14889:2003)




149.


EN 14931:2006
Pressure vessels for human occupancy (PVHO) - Multi-place pressure chamber systems for hyperbaric therapy - Performance, safety requirements and testing




150.


EN ISO 14937:2009
Sterilization of health care products - General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices (ISO 14937:2009)




151.


EN ISO 14971:2012
Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01)




152.


EN ISO 15001:2011
Anaesthetic and respiratory equipment - Compatibility with oxygen (ISO 15001:2010)




153.


EN ISO 15002:2008
Flow-metering devices for connection to terminal units of medical gas pipeline systems (ISO 15002:2008)




154.


EN ISO 15004-1:2009
Ophthalmic instruments - Fundamental requirements and test methods - Part 1: General requirements applicable to all ophthalmic instruments (ISO 15004-1:2006)




155.


EN ISO 15223-1:2016
Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements (ISO 15223-1:2016, Corrected version 2017-03)




156.


EN ISO 15747:2019
Plastic containers for intravenous injections (ISO 15747:2018)




157.


EN ISO 15798:2010
Ophthalmic implants - Ophthalmic viscosurgical devices (ISO 15798:2010)




158.


EN ISO 15883-1:2009
Washer-disinfectors - Part 1: General requirements, terms and definitions and tests (ISO 15883-1:2006)




159.


EN ISO 15883-2:2009
Washer-disinfectors - Part 2: Requirements and tests for washer-disinfectors employing thermal disinfection for surgical instruments, anaesthetic equipment, bowls, dishes, receivers, utensils, glassware, etc. (ISO 15883-2:2006)




160.


EN ISO 15883-3:2009
Washer-disinfectors - Part 3: Requirements and tests for washer-disinfectors employing thermal disinfection for human waste containers (ISO 15883-3:2006)




161.


EN ISO 15883-4:2018
Washer-disinfectors - Part 4: Requirements and tests for washer-disinfectors employing chemical disinfection for thermolabile endoscopes (ISO 15883-4:2018)




162.


EN 15986:2011
Symbol for use in the labelling of medical devices - Requirements for labelling of medical devices containing phthalate




163.


EN ISO 16061:2009
Instrumentation for use in association with non- active surgical implants - General requirements (ISO 16061:2008, Corrected version 2009-03- 15)




164.


EN ISO 16201:2006
Technical aids for disabled persons - Environmental control systems for daily living (ISO 16201:2006)




165.


EN ISO 17510-1:2009
Sleep apnoea breathing therapy - Part 1: Sleep apnoea breathing therapy equipment (ISO 17510-1:2007)




166.


EN ISO 17510-2:2009
Sleep apnoea breathing therapy - Part 2: Masks and application accessories (ISO 17510-2:2007)




167.


EN ISO 17664:2017
Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices (ISO 17664:2017)




168.


EN ISO 17665-1:2006
Sterilization of health care products - Moist heat - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 17665-1:2006)




169.


EN ISO 18777:2009
Transportable liquid oxygen systems for medical use - Particular requirements (ISO 18777:2005)




170.


EN ISO 18778:2009
Respiratory equipment - Infant monitors - Particular requirements (ISO 18778:2005)




171.


EN ISO 18779:2005
Medical devices for conserving oxygen and oxygen mixtures - Particular requirements (ISO 18779:2005)




172.


EN ISO 19054:2006
Rail systems for supporting medical equipment (ISO 19054:2005)




173.


EN 20594-1:1993
Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment - Part 1: General requirements (ISO 594-1:1986)
EN 20594-1:1993/A1:1997
EN 20594-1:1993/AC:1996




174.


EN ISO 21534:2009
Non-active surgical implants - Joint replacement implants - Particular requirements (ISO 21534:2007)




175.


EN ISO 21535:2009
Non-active surgical implants - Joint replacement implants - Specific requirements for hip- joint replacement implants (ISO 21535:2007)




176.


EN ISO 21536:2009
Non-active surgical implants - Joint replacement implants - Specific requirements for knee- joint replacement implants (ISO 21536:2007)




177.


EN ISO 21649:2009
Needle-free injectors for medical use - Requirements and test methods (ISO 21649:2006)




178.


EN ISO 21969:2009
High-pressure flexible connections for use with medical gas systems (ISO 21969:2009)




179.


EN ISO 21987:2017
Ophthalmic optics - Mounted spectacle lenses (ISO 21987:2017)




180.


EN ISO 22442-1:2007
Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO 22442-1:2007)




181.


EN ISO 22442-2:2007
Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO 22442-2:2007)




182.


EN ISO 22442-3:2007
Medical devices utilizing animal tissues and their derivatives - Part 3: Validation of the elimination and/or inactivation of viruses and transmissible spongiform encephalopathy (TSE) agents (ISO 22442-3:2007)




183.


EN ISO 22523:2006
External limb prostheses and external orthoses - Requirements and test methods (ISO 22523:2006)
Notice: This standard still needs to be amended to take into account the requirements introduced by Directive 2007/47/EC. The amended standard will be published by CEN as soon as possible. Manufacturers are advised to check whether all relevant essential requirements of the amended directive are appropriately covered.




184.


EN ISO 22675:2016
Prosthetics - Testing of ankle-foot devices and foot units - Requirements and test methods (ISO 22675:2016)




185.


EN ISO 23328-1:2008
Breathing system filters for anaesthetic and respiratory use - Part 1: Salt test method to assess filtration performance (ISO 23328- 1:2003)




186.


EN ISO 23328-2:2009
Breathing system filters for anaesthetic and respiratory use - Part 2: Non-filtration aspects (ISO 23328-2:2002)




187.


EN ISO 23747:2009
Anaesthetic and respiratory equipment - Peak expiratory flow meters for the assessment of pulmonary function in spontaneously breathing humans (ISO 23747:2007)




188.


EN ISO 25424:2019
Sterilization of health care products - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 25424:2018)




189.


EN ISO 25539-1:2009
Cardiovascular implants - Endovascular devices - Part 1: Endovascular prostheses (ISO 25539-1:2003 including Amd 1:2005)
EN ISO 25539-1:2009/AC:2011




190.


EN ISO 25539-2:2009
Cardiovascular implants - Endovascular devices - Part 2: Vascular stents (ISO 25539- 2:2008)
EN ISO 25539-2:2009/AC:2011




191.


EN ISO 26782:2009
Anaesthetic and respiratory equipment - Spirometers intended for the measurement of time forced expired volumes in humans (ISO 26782:2009)
EN ISO 26782:2009/AC:2009




192.


EN 27740:1992
Instruments for surgery, scalpels with detachable blades, fitting dimensions (ISO 7740:1985)
EN 27740:1992/A1:1997
EN 27740:1992/AC:1996




193.


EN 60118-13:2005
Electroacoustics - Hearing aids - Part 13: Electromagnetic compatibility (EMC) (IEC 60118-13:2004)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




194.


EN 60522:1999
Determination of the permanent filtration of X- ray tube assemblies (IEC 60522:1999)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




195.


EN 60580:2000
Medical electrical equipment - Dose area product meters (IEC 60580:2000)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




196.


EN 60601-1:2006
Medical electrical equipment - Part 1: General requirements for basic safety and essential performance (IEC 60601-1:2005)
EN 60601-1:2006/AC:2010
EN 60601-1:2006/A1:2013 (IEC 60601-1:2005/A1:2012)




197.


EN 60601-1-1:2001
Medical electrical equipment - Part 1-1: General requirements for safety - Collateral standard: Safety requirements for medical electrical systems (IEC 60601-1-1:2000)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




198.


EN 60601-1-2:2015
Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests (IEC 60601-1-2:2014)




199.


EN 60601-1-3:2008
Medical electrical equipment - Part 1-3: General requirements for basic safety and essential performance - Collateral Standard: Radiation protection in diagnostic X-ray equipment (IEC 60601-1-3:2008)
EN 60601-1-3:2008/AC:2010
EN 60601-1-3:2008/A11:2016
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




200.


EN 60601-1-4:1996
Medical electrical equipment - Part 1-4: General requirements for safety - Collateral standard: Programmable electrical medical systems (IEC 60601-1-4:1996)
EN 60601-1-4:1996/A1:1999 (IEC 60601-1-4:1996/A1:1999)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




201.


EN 60601-1-6:2010
Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability (IEC 60601-1-6:2010)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




202.


EN 60601-1-8:2007
Medical electrical equipment - Part 1-8: General requirements for basic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems in medical electrical equipment and medical electrical systems (IEC 60601-1-8:2006)
EN 60601-1-8:2007/AC:2010
EN 60601-1-8:2007/A11:2017
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




203.


EN 60601-1-10:2008
Medical electrical equipment - Part 1-10: General requirements for basic safety and essential performance - Collateral Standard: Requirements for the development of physiologic closed-loop controllers (IEC 60601-1-10:2007)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




204.


EN 60601-1-11:2010
Medical electrical equipment - Part 1-11: General requirements for basic safety and essential performance - Collateral standard: Requirements for medical electrical equipment and medical electrical systems used in the home healthcare environment (IEC 60601-1-11:2010)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




205.


EN 60601-2-1:1998
Medical electrical equipment - Part 2-1: Particular requirements for the safety of electron accelerators in the range of 1 MeV to 50 MeV (IEC 60601-2-1:1998)
EN 60601-2-1:1998/A1:2002 (IEC 60601-2-1:1998/A1:2002)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




206.


EN 60601-2-2:2009
Medical electrical equipment - Part 2-2: Particular requirements for the basic safety and essential performance of high frequency surgical equipment and high frequency surgical accessories (IEC 60601-2-2:2009)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




207.


EN 60601-2-3:1993
Medical electrical equipment - Part 2: Particular requirements for the safety of short-wave therapy equipment (IEC 60601-2-3:1991)
EN 60601-2-3:1993/A1:1998 (IEC 60601-2-3:1991/A1:1998)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




208.


EN 60601-2-4:2003
Medical electrical equipment - Part 2-4: Particular requirements for the safety of cardiac defibrillators (IEC 60601-2-4:2002)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




209.


EN 60601-2-5:2000
Medical electrical equipment - Part 2-5: Particular requirements for the safety of ultrasonic physiotherapy equipment (IEC 60601-2-5:2000)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




210.


EN 60601-2-8:1997
Medical electrical equipment - Part 2: Particular requirements for the safety of therapeutic X-ray equipment operating in the range 10 kV to 1 MV (IEC 60601-2-8:1987)
EN 60601-2-8:1997/A1:1997 (IEC 60601-2-8:1987/A1:1997)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




211.


EN 60601-2-10:2000
Medical electrical equipment - Part 2-10: Particular requirements for the safety of nerve and muscle stimulators (IEC 60601-2-10:1987)
EN 60601-2-10:2000/A1:2001 (IEC 60601-2-10:1987/A1:2001)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




212.


EN 60601-2-11:1997
Medical electrical equipment - Part 2-11: Particular requirements for the safety of gamma beam therapy equipment (IEC 60601-2-11:1997)
EN 60601-2-11:1997/A1:2004 (IEC 60601-2-11:1997/A1:2004)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




213.


EN 60601-2-12:2006
Medical electrical equipment - Part 2-12: Particular requirements for the safety of lung ventilators - Critical care ventilators (IEC 60601-2-12:2001)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




214.


EN 60601-2-13:2006
Medical electrical equipment - Part 2-13: Particular requirements for the safety and essential performance of anaesthetic systems (IEC 60601-2-13:2003)
EN 60601-2-13:2006/A1:2007 (IEC 60601-2-13:2003/A1:2006)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




215.


EN 60601-2-16:1998
Medical electrical equipment - Part 2-16: Particular requirements for the safety of haemodialysis, haemodiafiltration and haemofiltration equipment (IEC 60601-2-16:1998)
EN 60601-2-16:1998/AC:1999
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




216.


EN 60601-2-17:2004
Medical electrical equipment - Part 2-17: Particular requirements for the safety of automatically-controlled brachytherapy afterloading equipment (IEC 60601-2-17:2004)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




217.


EN 60601-2-18:1996
Medical electrical equipment - Part 2-18: Particular requirements for the safety of endoscopic equipment (IEC 60601-2-18:1996)
EN 60601-2-18:1996/A1:2000 (IEC 60601-2-18:1996/A1:2000)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




218.


EN 60601-2-19:2009
Medical electrical equipment - Part 2-19: Particular requirements for the basic safety and essential performance of infant incubators (IEC 60601-2-19:2009)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




219.


EN 60601-2-20:2009
Medical electrical equipment - Part 2-20: Particular requirements for the basic safety and essential performance of infant transport incubators (IEC 60601-2-20:2009)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




220.


EN 60601-2-21:2009
Medical electrical equipment - Part 2-21: Particular requirements for the basic safety and essential performance of infant radiant warmers (IEC 60601-2-21:2009)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




221.


EN 60601-2-22:1996
Medical electrical equipment - Part 2: Particular requirements for the safety of diagnostic and therapeutic laser equipment (IEC 60601-2-22:1995)
Notice: This European Standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




222.


EN 60601-2-23:2000
Medical electrical equipment - Part 2-23: Particular requirements for the safety, including essential performance, of transcutaneous partial pressure monitoring equipment (IEC 60601-2-23:1999)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




223.


EN 60601-2-24:1998
Medical electrical equipment - Part 2-24: Particular requirements for the safety of infusion pumps and controllers (IEC 60601-2-24:1998)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




224.


EN 60601-2-25:1995
Medical electrical equipment - Part 2-25: Particular requirements for the safety of electrocardiographs (IEC 60601-2-25:1993)
EN 60601-2-25:1995/A1:1999 (IEC 60601-2-25:1993/A1:1999)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




225.


EN 60601-2-26:2003
Medical electrical equipment - Part 2-26: Particular requirements for the safety of electroencephalographs (IEC 60601-2-26:2002)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




226.


EN 60601-2-27:2006
Medical electrical equipment - Part 2-27: Particular requirements for the safety, including essential performance, of electrocardiographic monitoring equipment (IEC 60601-2-27:2005)
EN 60601-2-27:2006/AC:2006
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




227.


EN 60601-2-28:2010
Medical electrical equipment - Part 2-28: Particular requirements for the basic safety and essential performance of X-ray tube assemblies for medical diagnosis (IEC 60601-2-28:2010)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




228.


EN 60601-2-29:2008
Medical electrical equipment - Part 2-29: Particular requirements for the basic safety and essential performance of radiotherapy simulators (IEC 60601-2-29:2008)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




229.


EN 60601-2-30:2000
Medical electrical equipment - Part 2-30: Particular requirements for the safety, including essential performance, of automatic cycling non- invasive blood pressure monitoring equipment (IEC 60601-2-30:1999)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




230.


EN 60601-2-33:2010
Medical electrical equipment - Part 2-33: Particular requirements for the basic safety and essential performance of magnetic resonance equipment for medical diagnosis (IEC 60601-2-33:2010)
EN 60601-2-33:2010/A1:2015 (IEC 60601-2-33:2010/A1:2013)
EN 60601-2-33:2010/A2:2015 (IEC 60601-2-33:2010/A2:2015)
EN 60601-2-33:2010/AC:2016-03
EN 60601-2-33:2010/A12:2016




231.


EN 60601-2-34:2000
Medical electrical equipment - Part 2-34: Particular requirements for the safety, including essential performance, of invasive blood pressure monitoring equipment (IEC 60601-2-34:2000)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




232.


EN 60601-2-36:1997
Medical electrical equipment - Part 2: Particular requirements for the safety of equipment for extracorporeally induced lithotripsy (IEC 60601-2-36:1997)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




233.


EN 60601-2-37:2008
Medical electrical equipment - Part 2-37: Particular requirements for the basic safety and essential performance of ultrasonic medical diagnostic and monitoring equipment (IEC 60601-2-37:2007)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




234.


EN 60601-2-39:2008
Medical electrical equipment - Part 2-39: Particular requirements for basic safety and essential performance of peritoneal dialysis equipment (IEC 60601-2-39:2007)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




235.


EN 60601-2-40:1998
Medical electrical equipment - Part 2-40: Particular requirements for the safety of electromyographs and evoked response equipment (IEC 60601-2-40:1998)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




236.


EN 60601-2-41:2009
Medical electrical equipment - Part 2-41: Particular requirements for basic safety and essential performance of surgical luminaires and luminaires for diagnosis (IEC 60601-2-41:2009)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




237.


EN 60601-2-43:2010
Medical electrical equipment - Part 2-43: Particular requirements for basic safety and essential performance of X-ray equipment for interventional procedures (IEC 60601-2-43:2010)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




238.


EN 60601-2-44:2009
Medical electrical equipment - Part 2-44: Particular requirements for the basic safety and essential performance of X-ray equipment for computed tomography (IEC 60601-2-44:2009)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




239.


EN 60601-2-45:2001
Medical electrical equipment - Part 2-45: Particular requirements for the safety of mammographic X-ray equipment and mammographic stereotactic devices (IEC 60601-2-45:2001)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




240.


EN 60601-2-46:1998
Medical electrical equipment - Part 2-46: Particular requirements for the safety of operating tables (IEC 60601-2-46:1998)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




241.


EN 60601-2-47:2001
Medical electrical equipment - Part 2-47: Particular requirements for the safety, including essential performance, of ambulatory electrocardiographic systems (IEC 60601-2-47:2001)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




242.


EN 60601-2-49:2001
Medical electrical equipment - Part 2-49: Particular requirements for the safety of multifunction patient monitoring equipment (IEC 60601-2-49:2001)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




243.


EN 60601-2-50:2009
Medical electrical equipment - Part 2-50: Particular requirements for the basic safety and essential performance of infant phototherapy equipment (IEC 60601-2-50:2009)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




244.


EN 60601-2-51:2003
Medical electrical equipment - Part 2-51: Particular requirements for safety, including essential performance, of recording and analysing single channel and multichannel electrocardiographs (IEC 60601-2-51:2003)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




245.


EN 60601-2-52:2010
Medical electrical equipment - Part 2-52: Particular requirements for basic safety and essential performance of medical beds (IEC 60601-2-52:2009)
EN 60601-2-52:2010/AC:2011
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




246.


EN 60601-2-54:2009
Medical electrical equipment - Part 2-54: Particular requirements for the basic safety and essential performance of X-ray equipment for radiography and radioscopy (IEC 60601-2-54:2009)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




247.


EN 60627:2001
Diagnostic X-ray imaging equipment - Characteristics of general purpose and mammographic anti-scatter grids (IEC 60627:2001)
EN 60627:2001/AC:2002
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




248.


EN 60645-1:2001
Electroacoustics - Audiological equipment - Part 1: Pure-tone audiometers (IEC 60645-1:2001)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




249.


EN 60645-2:1997
Audiometers - Part 2: Equipment for speech audiometry (IEC 60645-2:1993)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




250.


EN 60645-3:2007
Electroacoustics - Audiometric equipment - Part 3: Test signals of short duration (IEC 60645-3:2007)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




251.


EN 60645-4:1995
Audiometers - Part 4: Equipment for extended high-frequency audiometry (IEC 60645-4:1994)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




252.


EN 61217:2012
Radiotherapy equipment - Coordinates, movements and scales (IEC 61217:2011)




253.


EN 61676:2002
Medical electrical equipment - Dosimetric instruments used for non-invasive measurement of X-ray tube voltage in diagnostic radiology (IEC 61676:2002)
EN 61676:2002/A1:2009 (IEC 61676:2002/A1:2008)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




254.


EN 62083:2009
Medical electrical equipment - Requirements for the safety of radiotherapy treatment planning systems (IEC 62083:2009)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




255.


EN 62220-1:2004
Medical electrical equipment - Characteristics of digital X-ray imaging devices - Part 1: Determination of the detective quantum efficiency (IEC 62220-1:2003)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




256.


EN 62220-1-2:2007
Medical electrical equipment - Characteristics of digital X-ray imaging devices - Part 1-2: Determination of the detective quantum efficiency - Detectors used in mammography (IEC 62220-1-2:2007)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




257.


EN 62220-1-3:2008
Medical electrical equipment - Characteristics of digital X-ray imaging devices - Part 1-3: Determination of the detective quantum efficiency - Detectors used in dynamic imaging (IEC 62220-1-3:2008)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




258.


EN 62304:2006
Medical device software - Software life-cycle processes (IEC 62304:2006)
EN 62304:2006/AC:2008
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




259.


EN 62366:2008
Medical devices - Application of usability engineering to medical devices (IEC 62366:2007)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




260.


EN 80601-2-35:2009
Medical electrical equipment - Part 2-35: Particular requirements for the basic safety and essential performance of heating devices using blankets, pads and mattresses and intended for heating in medical use (IEC 80601-2-35:2009)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




261.


EN 80601-2-58:2009
Medical electrical equipment - Part 2-58: Particular requirements for the basic safety and essential performance of lens removal devices and vitrectomy devices for ophthalmic surgery (IEC 80601-2-58:2008)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




262.


EN 80601-2-59:2009
Medical electrical equipment - Part 2-59: Particular requirements for the basic safety and essential performance of screening thermographs for human febrile temperature screening (IEC 80601-2-59:2008)
Notice: This European standard does not necessarily cover the requirements introduced by Directive 2007/47/EC.




263.


EN ISO 81060-1:2012
Non-invasive sphygmomanometers - Part 1: Requirements and test methods for non-automated measurement type (ISO 81060-1:2007)




264.


EN ISO 81060-2:2019
Non-invasive sphygmomanometers - Part 2: Clinical investigation of intermittent automated measurement type (ISO 81060-2:2018)









ANNEX II






No


Reference of the standard




1.


EN ISO 10993-11:2009
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006)




2.


EN ISO 11137-1:2015
Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006, including Amd 1:2013)




3.


EN ISO 11990-1:2014
Lasers and laser-related equipment - Determination of laser resistance of tracheal tubes - Part 1: Tracheal tube shaft (ISO 11990-1:2011)




4.


EN ISO 11990-2:2014
Lasers and laser-related equipment - Determination of laser resistance of tracheal tubes - Part 2: Tracheal tube cuffs (ISO 11990-2:2010)




5.


EN ISO 13408-2:2011
Aseptic processing of health care products - Part 2: Filtration (ISO 13408-2:2003)




6.


EN ISO 13485:2016
Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2016)
EN ISO 13485:2016/AC:2016




7.


EN 13976-2:2011
Rescue systems - Transportation of incubators - Part 2: System requirements




8.


EN 14683:2005
Surgical masks - Requirements and test methods




9.


EN ISO 15747:2011
Plastic containers for intravenous injections (ISO 15747:2010)




10.


EN ISO 15883-4:2009
Washer-disinfectors - Part 4: Requirements and tests for washer-disinfectors employing chemical disinfection for thermolabile endoscopes (ISO 15883-4:2008)




11.


EN ISO 17664:2004
Sterilization of medical devices - Information to be provided by the manufacturer for the processing of resterilizable medical devices (ISO 17664:2004)




12.


EN ISO 21987:2009
Ophthalmic optics - Mounted spectacle lenses (ISO 21987:2009)