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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 20594-1/AC:1996

Status: ANULADA / 2020-06-01

Conical fittings with 6 % (Luer) taper for syringes, needles and certain other medical equipment - Part 1: General requirements (ISO 594-1:1986)

UNE-EN 20594-1/A1:1998

Status: ANULADA / 2020-06-01

Conical fittings with a 6% (Luer) taper for syringes, needles and certain other medical equipment - Part 1: General requirements (ISO 594-1:1986)

UNE-EN 20594-1:1994

Status: ANULADA / 2020-06-01

Conical fittings with a 6% (Luer) taper for syringes, needles and certain other medical equipment - Part 1: General requirements (ISO 594-1:1986)

UNE-EN ISO 18472:2007

Status: ANULADA / 2020-04-01

Sterilization of health care products - Biological and chemical indicators - Test equipment (ISO 18472:2006)

UNE-EN 13726-6:2003

Status: ANULADA / 2020-03-05

Non-active medical devices - Test methods for primary wound dressing - Part 6: Odour control

UNE-EN ISO 23907:2013

Status: ANULADA / 2020-03-01

Sharps injury protection - Requirements and test methods - Sharps containers (ISO 23907:2012)

UNE-EN ISO 14161:2010

Status: ANULADA / 2020-02-12

Sterilization of health care products - Biological indicators - Guidance for the selection, use and interpretation of results (ISO 14161:2009)

UNE-EN 13795:2011+A1:2013

Status: ANULADA / 2020-01-08

Surgical drapes, gowns and clean air suits, used as medical devices for patients, clinical staff and equipment - General requirements for manufacturers, processors and products, test methods, performance requirements and performance levels

UNE-EN 13976-1:2011

Status: ANULADA / 2020-01-01

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

UNE-EN 13976-2:2011

Status: ANULADA / 2020-01-01

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

UNE-EN 14683:2014

Status: ANULADA / 2019-12-04

Medical face masks - Requirements and test methods

UNE-EN ISO 13959:2016

Status: ANULADA / 2019-11-13

Water for haemodialysis and related therapies (ISO 13959:2014)

UNE-EN ISO 11663:2016

Status: ANULADA / 2019-11-13

Quality of dialysis fluid for haemodialysis and related therapies (ISO 11663:2014)

UNE-EN ISO 13958:2016

Status: ANULADA / 2019-11-13

Concentrates for haemodialysis and related therapies (ISO 13958:2014)

UNE-EN ISO 26722:2016

Status: ANULADA / 2019-11-13

Water treatment equipment for haemodialysis applications and related therapies (ISO 26722:2014)

UNE-EN ISO 23500:2016

Status: ANULADA / 2019-10-30

Guidance for the preparation and quality management of fluids for haemodialysis and related therapies (ISO 23500:2014)

UNE-EN 868-10:2009

Status: ANULADA / 2019-10-09

Packaging for terminally sterilized medical devices - Part 10: Adhesive coated nonwoven materials of polyolefines - Requirements and test methods

UNE-EN 868-5:2009

Status: ANULADA / 2019-10-09

Packaging for terminally sterilized medical devices - Part 5: Sealable pouches and reels of porous materials and plastic film construction - Requirements and test methods

UNE-EN 868-8:2009

Status: ANULADA / 2019-10-09

Packaging for terminally sterilized medical devices - Part 8: Re-usable sterilization containers for steam sterilizers conforming to EN 285 - Requirements and test methods

UNE-EN 868-9:2009

Status: ANULADA / 2019-10-09

Packaging for terminally sterilized medical devices - Part 9: Uncoated nonwoven materials of polyolefines - Requirements and test methods