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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 13408-6:2011/A1:2013

Status: ANULADA2022-02-16

Aseptic processing of health care products - Part 6: Isolator systems (ISO 13408-6:2005/Amd 1:2013)

UNE-EN ISO 22442-1:2016

Status: ANULADA2022-01-19

Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO 22442-1:2015)

UNE-EN ISO 22442-2:2016

Status: ANULADA2022-01-19

Medical devices utilizing animal tissues and their derivatives - Part 2: Controls on sourcing, collection and handling (ISO 22442-2:2015)

UNE-EN ISO 10993-1:2010

Status: ANULADA2021-10-06

Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2009)

UNE-EN ISO 10993-1:2010/AC:2010

Status: ANULADA2021-10-06

Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process - Technical Corrigendum 1 (ISO 10993-1:2009/Cor 1:2010)

UNE-EN ISO 14155:2012

Status: ANULADA2021-09-22

Clinical investigation of medical devices for human subjects - Good clinical practice (ISO 14155:2011)

UNE-EN 13623:2011

Status: ANULADA2021-09-01

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 ISO 14160:2012

Status: ANULADA2021-09-01

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 14160:2011)

UNE-EN ISO 8638:2014

Status: ANULADA2021-09-01

Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (ISO 8638:2010)

UNE-EN 28871:1994

Status: ANULADA2021-04-08

ELASTOMERIC PARTS FOR AQUEOUS PARENTERAL PREPARATIONS. (ISO 8871:1990).

UNE-EN ISO 10993-18:2009

Status: ANULADA2021-01-20

Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005)

UNE-EN ISO 8871-2:2005

Status: ANULADA2020-12-23

Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization (ISO 8871-2:2003)

UNE-EN ISO 8871-2:2005/A1:2014

Status: ANULADA2020-12-23

Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization - Amendment 1 (ISO 8871-2:2003/Amd 1:2005)

UNE-EN ISO 7886-3:2010

Status: ANULADA2020-12-23

Sterile hypodermic syringes for single use - Part 3: Auto-disable syringes for fixed-dose immunization (ISO 7886-3:2005)

UNE-EN ISO 7886-2:1998

Status: ANULADA2020-12-23

Sterile hypodermic syringes for single use - Part 2: Syringes for use with power-driven syringe pumps (ISO 7886-2:1996)

UNE-EN ISO 11737-2:2010

Status: ANULADA2020-12-16

Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO 11737-2:2009)

UNE-EN 455-1:2001

Status: ANULADA2020-11-11

MEDICAL GLOVES FOR SINGLE USE. PART 1: REQUIREMENTS AND TESTING FOR FREEDOM FROM HOLES.

UNE-EN 13718-1:2015

Status: ANULADA2020-11-11

Medical vehicles and their equipment - Air ambulances - Part 1: Requirements for medical devices used in air ambulances

UNE-EN 13718-2:2015

Status: ANULADA2020-11-11

Medical vehicles and their equipment - Air ambulances - Part 2: Operational and technical requirements for air ambulances

UNE-EN ISO 25424:2011

Status: ANULADA2020-10-14

Sterilization of medical devices - Low temperature steam and formaldehyde - Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 25424:2009)