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Committee

Committee:

CTN 111 - Surgical and medical devices

Secretary:
FENIN - FEDERACIÓN ESPAÑOLA DE EMPRESAS DE TECNOLOGÍA SANITARIA
Field of Activity:
Standardization of:

- Transfusion, infusion, and injection equipment and accessories for medical use, in their aspects of terms and definitions, general characteristics, test methods and function suitability as well as standardization of containers and primary and secondary packaging (such as elastomeric and metallic closures);

- Surgical instruments and medical equipment in their aspects of terms and definitions, general characteristics, test methods and function suitability;

- Sterilization: Characteristics, validation and control methods of sterilizers and sterilization processes;

- Content, safety requirements and test methods for first aid kits;

- Sterile and disposable medical devices, concerning terminology, general characteristics, test methods and appropriate performance

Excluding:

- Anaesthetic and respiratory equipment;

- Aspects concerning safety of the electrical and electronic equipment;

- Aspects related to quality of the materials which are within the scope of other technical committees.
Structure:

SC 1 Terminology

SC 2 Disposable material

SC 3 Sistemas de gestión

SC 7 Sterilization

SC 9 Equipment for emergency services

SC 11 Surgical instruments

SC 13 Infusion, injection and transfusion equipments and devices

SC 14 Antiseptics and disinfectants

SC 15 Mechanical contraceptives

GT 1 Sistemas cerrados

International Relations:

ISO/TC 76  Transfusion, infusion and injection, and blood processing equipment for medical and pharmaceutical use

ISO/TC 84  Devices for administration of medicinal products and catheters

ISO/TC 157  Non-systemic contraceptives and STI barrier prophylactics

ISO/TC 170  Surgical instruments

ISO/TC 194  Biological and clinical evaluation of medical devices

ISO/TC 198  Sterilization of health care products

ISO/TC 210  Quality management and corresponding general aspects for products with a health purpose including medical devices

CEN/CLC/JTC 3  Quality management and corresponding general aspects for medical devices

CEN/CLC/SAG Action Plan on Climate change  Healthcare Standards

CEN/CLC/SAG Healthcare Standards  Healthcare Standards

CEN/ABHS  Advisory Board for Health Standards

CEN/SS S02  Transfusion equipment

CEN/SS S03  Syringes

CEN/SS S99  Health, environment and medical equipment - Undetermined

CEN/TC 102  Sterilizers and associated equipment for processing of medical devices

CEN/TC 204  Sterilization of medical devices

CEN/TC 205  Non-active medical devices

CEN/TC 206  Biological and clinical evaluation of medical devices

CEN/TC 216  Chemical disinfectants and antiseptics

CEN/TC 239  Rescue systems

* Some activities of this TC correspond to other AEN/CTN.

Standards developed by the committee: CTN 111: 832

UNE-EN ISO 13485:2016/AC:2017

Status: ANULADA2018-07-25

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

UNE-EN ISO 17664:2004

Status: ANULADA2018-06-20

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

UNE-EN ISO 11137-3:2007

Status: ANULADA2018-05-16

Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects (ISO 11137-3:2006)

UNE-EN ISO 10993-16:2010

Status: ANULADA2018-05-16

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

UNE-EN 1060-3:1997+A2:2010

Status: ANULADA2018-05-03

Non-invasive sphygmomanometers - Part 3: Supplementary requirements for electro-mechanical blood pressure measuring systems

UNE-EN ISO 15225:2016

Status: ANULADA2018-02-08

Medical devices - Quality management - Medical device nomenclature data structure (ISO 15225:2016)

UNE-EN 12791:2016

Status: ANULADA2018-01-24

Chemical disinfectants and antiseptics - Surgical hand disinfection - Test method and requirements (phase 2, step 2)

UNE-EN ISO 10993-4:2017

Status: ANULADA2018-01-24

Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2017)

UNE-EN ISO 4074:2002

Status: ANULADA2017-12-01

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

UNE-EN ISO 4074:2002/AC:2008

Status: ANULADA2017-12-01

Natural latex rubber condoms - Requirements and test methods (ISO 4074:2002/Cor 2:2008)

UNE-EN ISO 4074/AC:2004

Status: ANULADA2017-12-01

Natural latex rubber condoms - Requirements and test methods (ISO 4074:2002/Cor.1:2003)

UNE-EN ISO 10993-4:2009

Status: ANULADA2017-11-15

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

UNE-EN ISO 11138-1:2007

Status: ANULADA2017-11-08

Sterilization of health care products - Biological indicators - Part 1: General requirements (ISO 11138-1:2006)

UNE-EN ISO 11138-2:2009

Status: ANULADA2017-11-08

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

UNE-EN 868-2:2009

Status: ANULADA2017-11-02

Packaging for terminally sterilized medical devices - Part 2: Sterilization wrap - Requirements and test methods

UNE-EN 868-3:2009

Status: ANULADA2017-11-02

Packaging for terminally sterilized medical devices - Part 3: Paper for use in the manufacture of paper bags (specified in EN 868-4) and in the manufacture of pouches and reels (specified in EN 868-5) - Requirements and test methods

UNE-EN 868-4:2009

Status: ANULADA2017-11-02

Packaging for terminally sterilized medical devices - Part 4: Paper bags - Requirements and test methods

UNE-EN 868-6:2009

Status: ANULADA2017-11-02

Packaging for terminally sterilized medical devices - Part 6: Paper for low temperature sterilization processes - Requirements and test methods

UNE-EN 868-7:2009

Status: ANULADA2017-11-02

Packaging for terminally sterilized medical devices - Part 7: Adhesive coated paper for low temperature sterilization processes - Requirements and test methods

UNE-EN ISO 10993-6:2009

Status: ANULADA2017-10-25

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