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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 14349:2008

Status: ANULADA2013-06-12

Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in veterinary area on non-porous surfaces without mechanical action - Test method and requirements (phase 2, step 2)

UNE-EN ISO 13485:2012

Status: ANULADA2013-05-29

Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003)

UNE-EN 13795:2011

Status: ANULADA2013-04-10

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 ISO 22413:2011

Status: ANULADA2013-04-03

Transfer sets for pharmaceutical preparations - Requirements and test methods (ISO 22413:2010)

UNE-EN ISO 8536-4:2011

Status: ANULADA2013-04-03

Infusion equipment for medical use - Part 4: Infusion sets for single use, gravity feed (ISO 8536-4:2010)

UNE-EN ISO 8536-5:2012

Status: ANULADA2013-04-03

Infusion equipment for medical use - Part 5: Burette infusion sets for single use, gravity feed (ISO 8536-5:2004)

UNE-EN 455-2:2010+A1:2011

Status: ANULADA2013-04-03

Medical gloves for single use - Part 2: Requirements and testing for physical properties

UNE-EN ISO 23908:2011

Status: ANULADA2013-04-03

Sharps injury protection - Requirements and test methods - Sharps protection features for single-use hypodermic needles, introducers for catheters and needles used for blood sampling (ISO 23908:2011)

UNE-EN ISO 20072:2011

Status: ANULADA2013-04-03

Aerosol drug delivery device design verification - Requirements and test methods (ISO 20072:2009)

UNE-EN ISO 11608-3:2001

Status: ANULADA2013-03-20

Pen-injectors for medical use - Part 3: Finished cartridges - Requirements and test methods. (ISO 11608-3:2000)

UNE-EN ISO 10993-12:2009

Status: ANULADA2013-02-27

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

UNE-EN 1865:2000

Status: ANULADA2012-11-28

SPECIFICATIONS FOR STRETCHERS AND OTHER PATIENT HANDLING EQUIPMENT USED IN ROAD AMBULANCES

UNE-EN ISO 14971:2009

Status: ANULADA2012-11-28

Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01)

UNE-EN 13727:2004

Status: ANULADA2012-10-31

Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity of chemical disinfectants for instruments used in the medical area - Test method and requirements (phase 2, step 1)

UNE-EN ISO 11137-2:2007 ERRATUM:2010

Status: ANULADA2012-10-03

Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2006, corrected version 2006-08-01)

UNE-EN ISO 11137-2:2007

Status: ANULADA2012-10-03

Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2006, corrected version 2006-08-01)

UNE-EN ISO 1135-4:2011

Status: ANULADA2012-05-23

Transfusion equipment for medical use - Part 4: Transfusion sets for single use (ISO 1135-4:2010)

UNE-EN ISO 13485:2004

Status: ANULADA2012-05-23

Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003)

UNE-EN ISO 13485:2004 ERRATUM:2009

Status: ANULADA2012-05-23

Medical devices - Quality management systems - Requirements for regulatory purposes (ISO 13485:2003/Cor 1:2009)

UNE-EN ISO 15378:2008

Status: ANULADA2012-03-21

Primary packaging materials for medicinal products - Particular requirements for the application of ISO 9001:2000, with reference to Good Manufacturing Practice (GMP) (ISO 15378:2006)