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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 11139:2020/A1:2024

Status: VIGENTE / 2024-11-06

Sterilization of health care products - Vocabulary of terms used in sterilization and related equipment and process standards - Amendment 1: Amended and additional terms and definitions (ISO 11139:2018/Amd 1:2024)

UNE-EN ISO 17664-2:2024

Status: VIGENTE / 2024-11-06

Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - Part 2: Non-critical medical devices (ISO 17664-2:2021)

UNE-EN ISO 8362-2:2024

Status: VIGENTE / 2024-11-06

Injection containers and accessories - Part 2: Closures for injection vials (ISO 8362-2:2024)

UNE-EN ISO 8536-13:2024 (Ratificada)

Status: VIGENTE / 2024-11-01

Infusion equipment for medical use - Part 13: Graduated flow regulators for single use with fluid contact (ISO 8536-13:2024) (Endorsed by Asociación Española de Normalización in November of 2024.)

UNE-EN ISO 7199:2024 (Ratificada)

Status: VIGENTE / 2024-10-01

Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators) (ISO 7199:2024) (Endorsed by Asociación Española de Normalización in October of 2024.)

UNE-EN ISO 15378:2018/A1:2024

Status: VIGENTE / 2024-09-25

Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2015, with reference to good manufacturing practice (GMP) - Amendment 1: Climate action changes (ISO 15378:2017/Amd 1:2024)

UNE-EN ISO 10555-1:2024

Status: VIGENTE / 2024-09-11

Intravascular catheters - Sterile and single-use catheters - Part 1: General requirements (ISO 10555-1:2023)

UNE-EN ISO 10555-4:2024

Status: VIGENTE / 2024-07-17

Intravascular catheters - Sterile and single-use catheters - Part 4: Balloon dilatation catheters (ISO 10555-4:2023)

UNE-EN 1789:2021+A1:2024

Status: VIGENTE / 2024-07-17

Medical vehicles and their equipment - Road ambulances

UNE-EN 455-3:2024

Status: VIGENTE / 2024-06-19

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

UNE-EN 13697:2024

Status: VIGENTE / 2024-06-05

Chemical disinfectants and antiseptics - Quantitative non-porous surface test for the evaluation of bactericidal and yeasticidal and/or fungicidal activity of chemical disinfectants used in food, industrial, domestic and institutional areas without mechanical action - Test method and requirements without mechanical action (phase 2, step 2)

UNE-EN 17846:2024

Status: VIGENTE / 2024-06-05

Chemical disinfectants and antiseptics - Quantitative test method for the evaluation of sporicidal activity against Clostridioides difficile on non-porous surfaces with mechanical action employing wipes in the medical area (4-field test) - Test method and requirements (phase 2, step 2)

UNE-EN ISO 8637-2:2024 (Ratificada)

Status: VIGENTE / 2024-06-01

Extracorporeal systems for blood purification - Part 2: Extracorporeal blood and fluid circuits for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637-2:2024) (Endorsed by Asociación Española de Normalización in June of 2024.)

UNE-EN ISO 11607-1:2020/A1:2024

Status: VIGENTE / 2024-05-22

Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems - Amendment 1: Application of risk management (ISO 11607-1:2019/Amd 1:2023)

UNE-EN ISO 11607-2:2020/A1:2024

Status: VIGENTE / 2024-05-22

Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes - Amendment 1: Application of risk management (ISO 11607-2:2019/Amd 1:2023)

UNE-EN ISO 10993-17:2024

Status: VIGENTE / 2024-05-22

Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents (ISO 10993-17:2023)

UNE-EN ISO 10993-18:2021/A1:2024

Status: VIGENTE / 2024-05-22

Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process - Amendment 1: Determination of the uncertainty factor (ISO 10993-18:2020/Amd 1:2022)

UNE-EN 13726:2024

Status: VIGENTE / 2024-04-24

Test methods for wound dressings - Aspects of absorption, moisture vapour transmission, waterproofness and extensibility

UNE-EN 13976-1:2019

Status: VIGENTE / 2024-03-01

Rescue systems - Transportation of incubators - Part 1: Interface requirements

UNE-EN 13976-2:2019

Status: VIGENTE / 2024-03-01

Rescue systems - Transportation of incubators - Part 2: System requirements