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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: 830

UNE-EN ISO 10993-11:2018

Status: VIGENTE2018-12-26

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

UNE-EN ISO 11070:2015/A1:2018

Status: VIGENTE2018-12-26

Sterile single-use intravascular introducers, dilators and guidewires - Amendment 1 (ISO 11070:2014/Amd 1:2018)

UNE-EN ISO 8536-14:2018

Status: VIGENTE2018-11-21

Infusion equipment for medical use - Part 14: Clamps and flow regulators for transfusion and infusion equipment without fluid contact (ISO 8536-14:2016)

UNE-EN ISO 15378:2018

Status: VIGENTE2018-10-24

Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP) (ISO 15378:2017)

UNE-EN ISO 13408-2:2018

Status: VIGENTE2018-10-24

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

UNE-EN ISO 80601-2-56:2018

Status: VIGENTE2018-09-19

Medical electrical equipment - Part 2-56: Particular requirements for basic safety and essential performance of clinical thermometers for body temperature measurement (ISO 80601-2-56:2017)

UNE-EN ISO 13485:2018

Status: VIGENTE2018-07-25

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

UNE-EN ISO 11140-1:2015

Status: VIGENTE2018-06-20

Sterilization of health care products - Chemical indicators - Part 1: General requirements (ISO 11140-1:2014)

UNE-EN ISO 10555-6:2018

Status: VIGENTE2018-05-16

Intravascular catheters - Sterile and single-use catheters - Part 6: Subcutaneous implanted ports (ISO 10555-6:2015)

UNE-EN ISO 11137-3:2018

Status: VIGENTE2018-05-16

Sterilization of health care products - Radiation - Part 3: Guidance on dosimetric aspects of development, validation and routine control (ISO 11137-3:2017)

UNE-EN ISO 10993-16:2018

Status: VIGENTE2018-05-16

Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2017)

UNE-EN 13727:2012+A2:2015

Status: VIGENTE2018-01-31

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)

UNE-EN ISO 10993-4:2018

Status: VIGENTE2018-01-24

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

UNE-EN ISO 11608-7:2018

Status: VIGENTE2018-01-24

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

UNE-EN ISO 11138-1:2017

Status: VIGENTE2017-11-08

Sterilization of health care products - Biological indicators - Part 1: General requirements (ISO 11138-1:2017)

UNE-EN ISO 11138-2:2017

Status: VIGENTE2017-11-08

Sterilization of health care products - Biological indicators - Part 2: Biological indicators for ethylene oxide sterilization processes (ISO 11138-2:2017)

UNE-EN ISO 1135-3:2017

Status: VIGENTE2017-11-02

Transfusion equipment for medical use - Part 3: Blood-taking sets for single use (ISO 1135-3:2016)

UNE-EN 868-2:2017

Status: VIGENTE2017-11-02

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

UNE-EN 868-3:2017

Status: VIGENTE2017-11-02

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 868-4:2017

Status: VIGENTE2017-11-02

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