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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 22413:2022

Status: VIGENTE2022-03-16

Transfer sets for pharmaceutical preparations - Requirements and test methods (ISO 22413:2021)

UNE-EN ISO 11138-8:2022

Status: VIGENTE2022-03-16

Sterilization of health care products - Biological indicators - Part 8: Method for validation of a reduced incubation time for a biological indicator (ISO 11138-8:2021)

UNE-EN ISO 15223-1:2022

Status: VIGENTE2022-03-16

Medical devices - Symbols to be used with information to be supplied by the manufacturer - Part 1: General requirements (ISO 15223-1:2021)

UNE-EN ISO 11737-1:2018/A1:2022

Status: VIGENTE2022-02-16

Sterilization of health care products - Microbiological methods - Part 1: Determination of a population of microorganisms on products - Amendment 1 (ISO 11737-1:2018/Amd 1:2021)

UNE-EN ISO 10993-12:2022

Status: VIGENTE2022-02-16

Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2021)

UNE-EN ISO 13408-6:2022

Status: VIGENTE2022-02-16

Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2021)

UNE-EN ISO 22442-1:2022

Status: VIGENTE2022-01-19

Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO 22442-1:2020)

UNE-EN ISO 22442-2:2022

Status: VIGENTE2022-01-19

Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO 22442-2:2020)

UNE-EN ISO 20417:2021

Status: VIGENTE2022-01-05

Medical devices - Information to be supplied by the manufacturer (ISO 20417:2021, Corrected version 2021-12)

UNE-CEN ISO/TS 16775:2021 (Ratificada)

Status: VIGENTE2022-01-01

Packaging for terminally sterilized medical devices - Guidance on the application of ISO 11607-1 and ISO 11607-2 (ISO/TS 16775:2021) (Endorsed by Asociación Española de Normalización in January of 2022.)

UNE-EN ISO 10993-23:2021

Status: VIGENTE2021-10-13

Biological evaluation of medical devices - Part 23: Tests for irritation (ISO 10993-23:2021)

UNE-EN ISO 8536-12:2021

Status: VIGENTE2021-10-06

Infusion equipment for medical use - Part 12: Check valves for single use (ISO 8536-12:2021)

UNE-EN ISO 10993-1:2021

Status: VIGENTE2021-10-06

Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2018, including corrected version 2018-10)

UNE-EN ISO 14155:2021

Status: VIGENTE2021-09-22

Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2020)

UNE-EN 13623:2021

Status: VIGENTE2021-09-01

Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity against Legionella of chemical disinfectants for aqueous systems - Test method and requirements (phase 2, step 1)

UNE-EN 80369-5:2017/AC:2021-06

Status: VIGENTE2021-09-01

Small-bore connectors for liquids and gases in healthcare applications - Part 5: Connectors for limb cuff inflation applications

UNE-EN ISO 14160:2021 (Ratificada)

Status: VIGENTE2021-09-01

Sterilization of health care products - Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - Requirements for characterization, development, validation and routine control of a sterilization process for medical devices (ISO 14160:2020) (Endorsed by Asociación Española de Normalización in September of 2021.)

UNE-EN ISO 7886-1:2018

Status: VIGENTE2021-07-28

Sterile hypodermic syringes for single use - Part 1: Syringes for manual use (ISO 7886-1:2017, Corrected version 2019-08)

UNE-EN ISO 81060-2:2020/A1:2021

Status: VIGENTE2021-04-28

Non-invasive sphygmomanometers - Part 2: Clinical investigation of intermittent automated measurement type - Amendment 1 (ISO 81060-2:2018/Amd 1:2020)

UNE-EN ISO 10993-18:2021

Status: VIGENTE2021-01-20

Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)