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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 11607-1:2020/A11:2022

Status: VIGENTE / 2022-12-21

Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2019)

UNE-EN ISO 11607-2:2020/A11:2022

Status: VIGENTE / 2022-12-21

Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019)

UNE-EN ISO 25424:2020/A1:2022

Status: VIGENTE / 2022-12-21

Sterilization of health care products - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices - Amendment 1 (ISO 25424:2018/Amd 1:2022)

UNE-EN ISO 8536-15:2022

Status: VIGENTE / 2022-11-02

Infusion equipment for medical use - Part 15: Light-protective infusion sets for single use (ISO 8536-15:2022)

UNE-CEN/TR 17825:2022 (Ratificada)

Status: VIGENTE / 2022-10-01

Chemical disinfectants and antiseptics - Interpretation of water controls in EN 16615:2015 (Endorsed by Asociación Española de Normalización in October of 2022.)

UNE-EN ISO 13485:2018/A11:2022

Status: VIGENTE / 2022-09-21

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

UNE-EN 12353:2022

Status: VIGENTE / 2022-07-27

Chemical disinfectants and antiseptics - Preservation of test organisms used for the determination of bactericidal (including Legionella), mycobactericidal, sporicidal, fungicidal and virucidal (including bacteriophages) activity

UNE-EN ISO 10993-7:2009/A1:2022

Status: VIGENTE / 2022-07-27

Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals - Amendment 1: Applicability of allowable limits for neonates and infants (ISO 10993-7:2008/Amd 1:2019)

UNE-EN ISO 11608-1:2022 (Ratificada)

Status: VIGENTE / 2022-07-01

Needle-based injection systems for medical use - Requirements and test methods - Part 1: Needle-based injection systems (ISO 11608-1:2022) (Endorsed by Asociación Española de Normalización in July of 2022.)

UNE-EN ISO 11608-2:2022 (Ratificada)

Status: VIGENTE / 2022-07-01

Needle-based injection systems for medical use - Requirements and test methods - Part 2: Double-ended pen needles (ISO 11608-2:2022) (Endorsed by Asociación Española de Normalización in July of 2022.)

UNE-EN ISO 14971:2020/A11:2022

Status: VIGENTE / 2022-06-22

Medical devices - Application of risk management to medical devices (ISO 14971:2019)

UNE-EN 14931:2007

Status: VIGENTE / 2022-06-15

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

UNE-EN ISO 15883-5:2022

Status: VIGENTE / 2022-06-01

Washer-disinfectors - Part 5: Performance requirements and test method criteria for demonstrating cleaning efficacy (ISO 15883-5:2021)

UNE-EN ISO 17664-1:2022

Status: VIGENTE / 2022-06-01

Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 1: Critical and semi-critical medical devices (ISO 17664-1:2021)

UNE-EN ISO 10993-9:2022

Status: VIGENTE / 2022-05-25

Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2019)

UNE-EN 14347:2005

Status: VIGENTE / 2022-04-11

Chemical disinfectants and antiseptics - Basic sporicidal activity - Test method and requirements (phase 1, step 1)

UNE-EN 12791:2016+A1:2018

Status: VIGENTE / 2022-04-11

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

UNE-EN 13610:2003

Status: VIGENTE / 2022-04-11

Chemical disinfectants - Quantitative suspension test for the evaluation of virucidal activity against bacteriophages of chemical disinfectants used in food and industrial areas - Test method and requirements (phase 2, step 1)

UNE-EN 14683:2019+AC:2019

Status: VIGENTE / 2022-04-06

Medical face masks - Requirements and test methods

UNE-EN 17387:2022

Status: VIGENTE / 2022-03-16

Chemical disinfectants and antiseptics - Quantitative test for the evaluation of bactericidal and yeasticidal and/or fungicidal activity of chemical disinfectants in the medical area on non-porous surfaces without mechanical action - Test method and requirements (phase 2, step 2)