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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 13795-2:2005

Status: ANULADA2010-03-22

Surgical drapes, gowns and clean air suits, used as medical devices for patients, clinical staff and equipment - Part 2: Test methods

UNE-EN 13795-3:2007

Status: ANULADA2010-03-22

Surgical drapes, gowns and clean air suits, used as medical devices for patients, clinical staff and equipment - Part 3: Performance requirements and performance levels

UNE-EN ISO 14971:2007

Status: ANULADA2010-03-22

Medical devices - Application of risk management to medical devices (ISO 14971:2007)

UNE-EN 12470-1:2000

Status: ANULADA2010-03-22

CLINICAL THERMOMETERS. PART 1: METALLIC LIQUID-IN-GLASS THERMOMETERS WITH MAXIMUM DEVICE.

UNE-EN 12470-2:2001

Status: ANULADA2010-03-22

Clinical thermometers - Part 2: Phase change type (dot matrix) thermometers.

UNE-EN 12470-3:2000

Status: ANULADA2010-03-22

CLINICAL THERMOMETERS. PART 3: PERFORMANCE OF COMPACT ELECTRICAL THERMOMETERS (NON-PREDICTIVE AND PREDICTIVE) WITH MAXIMUM DEVICE

UNE-EN 12470-4:2001

Status: ANULADA2010-03-22

Clinical thermometers - Part 4: Performance of electrical thermometers for continuous measurement.

UNE-EN ISO 14971:2001

Status: ANULADA2010-03-10

Medical devices - Application of risk management to medical devices. (ISO 14971:2000)

UNE-EN ISO 14971/AC:2002

Status: ANULADA2010-03-10

Medical devices - Application of risk management to medical devices. (ISO 14971:2000)

UNE-EN ISO 14971/A1:2003

Status: ANULADA2010-03-10

Medical devices - Application of risk management to medical devices - Amendment 1: Rationale for requirements (ISO 14971:2000/AM1:2003)

UNE-ENV 12718:2002

Status: ANULADA2010-01-13

Medical compression hosiery.

UNE-ENV 12719:2002

Status: ANULADA2010-01-13

Medical thrombosis prophylaxis hosiery.

UNE-EN ISO 8536-3:2000

Status: ANULADA2009-12-16

INFUSION EQUIPMENT FOR MEDICAL USE. PART 3: ALUMINIUM CAPS FOR INFUSION BOTTLES (ISO 8536-3:1992)

UNE-EN ISO 10993-5:2002 ERRATUM

Status: ANULADA2009-12-09

Biological evaluation of medical devices. Part 5: Tests for in vitro cytotoxicity. (ISO 10993-5:1999)

UNE-EN ISO 10993-5:2000

Status: ANULADA2009-12-09

BIOLOGICAL EVALUATION OF MEDICAL DEVICES. PART 5: TESTS FOR IN VITRO CYTOTOXICITY (ISO 10993-5:1999)

UNE-EN 868-10:2000

Status: ANULADA2009-12-02

PACKAGING MATERIALS AND SYSTEMS FOR MEDICAL DEVICES WHICH ARE TO BE STERILIZED. PART 10: ADHESIVE COATED NONWOVEN MATERIALS OF POLYOLEFINES FOR USE IN THE MANUFACTURE OF HEAT SEALABLE POUCHES, REELS AND LIDS. REQUIREMENTS AND TEST METHODS

UNE-EN 868-2:2000

Status: ANULADA2009-12-02

PACKAGING MATERIALS AND SYSTEMS FOR MEDICAL DEVICES WHICH ARE TO BE STERILIZED. PART 2: STERILIZATION WRAP. REQUIREMENTS AND TEST METHODS.

UNE-EN 868-3:2000

Status: ANULADA2009-12-02

PACKAGING MATERIALS AND SYSTEMS FOR MEDICAL DEVICES WHICH ARE TO BE STERILIZED. PART 3: PAPER FOR USE IN THE MANUFACTURE OF PAPER BAGS (SPECIFIED IN EN 868-4) AND IN THE MANUFACTURE OF POUCHES AND REELS (SPECIFIED IN EN 868-5). REQUIREMENTS AND TEST METHODS.

UNE-EN 868-4:2000

Status: ANULADA2009-12-02

PACKAGING MATERIALS AND SYSTEMS FOR MEDICAL DEVICES WHICH ARE TO BE STERILIZED. PART 4: PAPER BAGS. REQUIREMENTS AND TEST METHODS.

UNE-EN 868-5:2000

Status: ANULADA2009-12-02

PACKAGING MATERIALS AND SYSTEMS FOR MEDICAL DEVICES WHICH ARE TO BE STERILIZED. PART 5: HEAT AND SELF-SEALABLE POUCHES AND REELS OF PAPER AND PLASTIC FILM CONSTRUCTION. REQUIREMENTS AND TEST METHODS.