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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 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: 851

UNE-EN ISO 10555-1/A2:2004

Status: ANULADA2010-03-22

Sterile, single-use intravascular catheters - Part 1: General requirements (ISO 10555-1:1996/AM 2:2004)

UNE-EN ISO 10555-1/A1:2000

Status: ANULADA2010-03-22

STERILE, SINGLE-USE INTRAVASCULAR CATHETERS. PART 1: GENERAL REQUIREMENTS (ISO 10555-1:1996/AM1:1999)

UNE-EN 13867:2003

Status: ANULADA2010-03-22

Concentrates for haemodialysis and related therapies.

UNE-EN ISO 11607-1:2007

Status: ANULADA2010-03-22

Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2006)

UNE-EN ISO 11138-2:2007

Status: ANULADA2010-03-22

Sterilization of health care products - Biological indicators - Part 2: Biological indicators for ethylene oxide sterilization processes (ISO 11138-2:2006)

UNE-EN ISO 11138-3:2007

Status: ANULADA2010-03-22

Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes (ISO 11138-3:2006)

UNE-EN ISO 11140-1:2006

Status: ANULADA2010-03-22

Sterilization of health care products - Chemical indicators - Part 1: General requirements (ISO 11140-1:2005)

UNE-EN ISO 11140-3:2007

Status: ANULADA2010-03-22

Sterilization of health care products - Chemical indicators - Part 3: Class 2 indicator systems for use in the Bowie and Dick-type steam penetration test (ISO 11140-3:2007)

UNE-EN ISO 11140-3:2007/AC:2008

Status: ANULADA2010-03-22

Sterilization of health care products - Chemical indicators - Part 3: Class 2 indicator systems for use in the Bowie and Dick-type steam penetration test (ISO 11140-3:2007/Cor 1:2007)

UNE-EN 285:2007+A1:2008

Status: ANULADA2010-03-22

Sterilization - Steam sterilizers - Large sterilizers

UNE-EN 13060:2005

Status: ANULADA2010-03-22

Small steam sterilizers

UNE-EN 14180:2004

Status: ANULADA2010-03-22

Sterilizers for medical purposes - Low temperature steam and formaldehyde sterilizers - Requirements and testing

UNE-EN 14180:2004+A1:2009

Status: ANULADA2010-03-22

Sterilizers for medical purposes - Low temperature steam and formaldehyde sterilizers - Requirements and testing

UNE-EN 1422:1998

Status: ANULADA2010-03-22

STERILIZERS FOR MEDICAL PURPOSES. ETHYLENE OXIDE STERILIZERS. REQUIREMENTS AND TEST METHODS.

UNE-EN 1422/AC:2002

Status: ANULADA2010-03-22

Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods.

UNE-EN ISO 10993-3:2004

Status: ANULADA2010-03-22

Biological evaluation of medical devices. Part 3: Tests for genotoxicity, carcinogenicty and reproductive toxicity (ISO10993-3:2003)

UNE-EN ISO 10993-10:2003

Status: ANULADA2010-03-22

Biological evaluation of medical devices. Part 10: Tests for irritation and delayed-type hypersensitivity. (ISO 10993-10:2002)

UNE-EN ISO 10993-10:2003/A1:2007

Status: ANULADA2010-03-22

Biological evaluation of medical devices - Part 10: Tests for irritation and delayed-type hypersensitivity - Amendment 1 (ISO 10993-10:2002/Amd 1:2006)

UNE-EN ISO 10993-11:2007

Status: ANULADA2010-03-22

Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006)

UNE-EN ISO 10993-12:2008

Status: ANULADA2010-03-22

Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2007)