Key Benefits:
In compliance with the provisions of Article 11 (f) of the Infrastructure Regulation for Industrial Quality and Safety, approved by Royal Decree 2200/1995 of 28 December 1995 ("BOE" of 6 February 1996), and the case for annulment of the rules submitted by the Spanish Association for Standardisation and Certification (AENOR), an entity designated by the Order of the Ministry of Industry and Energy of 26 February 1986, in accordance with Royal Decree 1614/1985 of 1 in August, and recognised by the additional provision of Royal Decree 2200/1995, of 28 December,
This Directorate-General has decided to publish, in the "Official State Gazette", the relationship of Spanish rules UNE cancelled during the month of March 2010, identified by its title and numerical code, which is listed as an annex to the Resolution.
Madrid, April 8, 2010. -Director General of Industry, Jesus Candil Gonzalo.
ANNEX
Rules cancelled in March 2010
Title | ||
---|---|---|
20317 /1M: 1993 |
Magnetic magnetothermic switches, for power control, 1.5 to 63 A. | |
20317:1988 | Switches Magnetothermic automatic, for power control, from 1.5 to 63 A. | |
UNE 20319:1978 | Electrical Material for Explosive Atmospheres. Internal overpressure wrappers | |
20321:1971 | Electrical material for explosive atmospheres with insulation filled with insulation pulverent. | |
20323:1978 | Electrical material for explosive atmospheres. Marks | |
UNE 20325 /1C: 1981 | Electrical Material for explosive atmospheres. Test method for the determination of the inflammation temperature | |
20325:1977 | Electrical material for explosive atmospheres. Test method for the determination of the inflammation temperature | |
20326:1970 | Electrical material immersed in oil for its use in explosive atmospheres | |
20543-5:1980 | Fixed condensers for electronic equipment. Mica capacitors for continuous current of nominal voltage not exceeding 3 000 V. Test methods and general requirements | |
20543-7:1982 | Fixed Condensers for Electronic Equipment. Polystyrene condensers for continuous current | |
20543-10:1984 | Fixed condensers for electronic equipment. Multi-layer ceramic dielectric chip capacitors. Test methods and general rules | |
20543-12:1982 | Fixed Condensers for Electronic Equipment. Polycarbonate capacitors, with metal armor, for continuous current | |
83609:1994 | Projected concrete and mortar. Determination of in situ compressive strength. Penetration/extraction test | |
UNE-CLC/TS 50354:2004 | Electrical arc test methods for materials and garments used by workers at risk of exposure to an electric arc | |
UNE-EN 285:2007 + A1:2008 | Sterilization. Steam sterilizers. Large sterilizers | |
UNE-EN 1422/AC: 2002 | Sterilizers for medical use. Sterilizers by ethylene oxide. Testing requirements and methods. | |
UNE-EN 1422:1998 | Sterilizers for medical use. Sterilizers by ethylene oxide. Testing requirements and methods | |
UNE-EN 12006-2:1998 | Non-active surgical implants. Particular requirements for cardiac and vascular implants. Part 2: Vascular protesis including heart valve ducts | |
UNE-EN 12006-3:1999 | Non-active surgical implants. Particular requirements for cardiac and vascular implants. Part 3: Endovascular products | |
UNE-EN 12470-1:2000 | Clinical thermometers. Part 1: Metal liquid dilation glass thermometers with maximum device | |
UNE-EN 12470-2:2001 | Clinical thermometers. Part 2: Phase-change thermometers (dot matrix). | |
UNE-EN 12470-3:2000 | Clinical thermometers. Part 3: Compact (comparison and extrapolation) electrical thermometers with maximum device | |
UNE-EN 12470-4:2001 | Termometers clinical. Part 4: Operation of electrical thermometers for continuous measurement | |
UNE-EN 13060:2005 | Water vapor sterilizers small. | |
UNE-EN 13795-1:2003 | Panos, gowns and suits for clean air of surgical use as sanitary products, for patients, clinical staff and equipment. Part 1: General requirements for manufacturers, processors, and products | |
UNE-EN 13795-2:2005 | Pans, gowns and suits for clean air surgical use as medical devices, for patients, clinical staff and equipment. Part 2: Test | |
UNE-EN 13795-3:2007 | Pans, gowns and suits for clean air of surgical use as medical devices, for patients, clinical staff and equipment. Part 3: Requirements and operating level | |
UNE-EN 13867:2003 | Concentric for hemodialysis and related therapies. | |
UNE-EN 14180:2004 | Sterilizers for medical use. Low temperature steam sterilizers and formaldehyde. Requirements and | |
UNE-EN 14180:2004 + A1:2009 | Sterilizers for medical use. Low temperature steam sterilizers and formaldehyde. Requirements and essays. | |
UNE-EN 14342:2006 | Wood flooring. Features, compliance assessment, and marking. | |
UNE-EN 14342 :2006/AC: 2007 | Wood flooring. Features, compliance assessment, and marking. | |
Railway applications. Electronic equipment used on rolling stock | ||
UNE-EN 50155/A1:2004 | Railway applications. Electronic equipment used on rolling stock | |
UNE-EN 50155:2002 | Railway applications. Electronic equipment used on rolling stock | |
UNE-EN 60269-1 CORR: 2004 | Low voltage fuses. Part 1: General requirements | |
UNE-EN 60269-1:2000 | Low voltage fuses. Part 1: General rules | |
Low-voltage fuses. Part 1: General | ||
UNE-EN 60335-2-34:2002/A11:2004 | Security of appliances and analogues. Part 2-34: Particular requirements for motor compressors | |
UNE-EN 60570 CORR: 1999 | Electrical Power Systems by Lane for luminaries. | |
UNE-EN 60570/A1:1999 | Electrical power systems per lane for luminaries. | |
UNE-EN 60570/A2:2001 | Power Systems electrical rail for luminaires. | |
UNE-EN 60570:1998 | Electrical power systems by rail for luminaires. | |
UNE-EN 60570-2-1/A1:1997 | Electrical power systems per lane for luminaries. Part 2: Mixed power systems. Section 1: Classes I and III | |
UNE-EN 60570-2-1:1996 | Electrical power systems per lane for luminaries. Part 2: Mixed power systems. Section 1: Classes I and III | |
UNE-EN 60684-3-246:2003 | Specifications for insulating flexible tubes. Part 3: Specific specifications for specific types of tubes. Sheet 246: Double-walled, non-flame-retarded polyolefin termorretractile tubes | |
UNE-EN 61181:1996 | Insulating Materials impregnated. Application of dissolved gas analysis (DGA) to electrical equipment factory testing | |
UNE-EN 61223-2-6:1996 | Evaluation trials and individual in medical imaging departments. Part 2-6: Constancy tests. X-ray equipment for computed tomography. | |
UNE-EN 61300-3-6:2004 | Optical fiber interconnect devices and passive components. Basic tests and measurement procedures. Part 3-6: Inspections and measures. Return loss. | |
UNE-EN 61557-1:1998 | Electrical security in low voltage distribution networks up to 1 000 V in c.a. and 1 500 V in c.c. Equipment for testing, measuring or monitoring protective measures. Part 1: General requirements | |
UNE-EN 61557-2:1998 | Electrical safety in low voltage distribution networks up to 1 000 V in c.a. and 1 500 V in c.c. Equipment for testing, measuring or monitoring protective measures. Part 2: Isolation resistance | |
UNE-EN 61557-2:1999 ERRATUM | Electrical safety in low voltage distribution networks up to 1 000 V in c.a. and 1 500 in c.c. Equipment for testing, measuring or monitoring protective measures. Part 2: Isolation resistance | |
UNE-EN 61557-3:1998 | Electrical safety in low voltage distribution networks up to 1 000 V in c.a. and 1 500 V in c.c. Equipment for testing, measuring or monitoring protective measures. Part 3: Loop impedance | |
UNE-EN 61557-4:1998 | Electrical security in low voltage distribution networks up to 1 000 V in c.a. and 1 500 V in c.c. Equipment for testing, measuring or monitoring protective measures. Part 4: Resistance of grounding conductors and equipotential connections | |
UNE-EN 61557-5:1998 | Electrical safety in networks low voltage distribution of up to 1 000 V in c.a. and 1 500 V in c.c. Equipment for testing, measuring or monitoring of protective measures. Part 5: Ground resistance | |
UNE-EN 61557-7:1998 | Electrical safety in low voltage distribution networks up to 1 000 V in c.a. and 1 500 V in c.c. Equipment for testing, measuring or monitoring protective measures. Part 7: Sequence of phases. | |
UNE-EN 62086-1:2006 | Electrical equipment for explosive gas atmospheres. Heaters for tracing by electrical resistance. Part 1: General and test requirements (IEC 62086-1:2001 + Corrigendum 1:2003) | |
UNE-EN 62086-2:2007 | Electrical material for atmospheres explosive gas. Heaters for tracing by electrical resistance. Part 2: Application Guide for Design, Installation and Maintenance. (IEC 62086-2:2001). | |
UNE-EN ISO 5360:2008 | anesthetic Vaporizers. Agent-specific filling systems (ISO 5360:2006) | |
UNE-EN ISO 5366-1:2005 | Respiratory and anesthesia equipment. Tracheostomy tubes. Part 1: Tubes and connectors for use in adults (ISO 5366-1:2000) | |
UNE-EN ISO 5840:2007 | Cardiovascular implants. Prosthetic heart valves. (ISO 5840:2005) | |
UNE-EN ISO 7197:2007 | Neurosurgical implants. Sterile, non-reusable bypass systems and components for hydrocephalus. (ISO 7197:2006) | |
UNE-EN ISO 7197 :2007/AC: 2008 | Neurosurgical implants. Sterile, non-reusable bypass systems and components for hydrocephalus. (ISO 7197 :2007/Cor 1:2007) | |
UNE-EN ISO 7376:2004 | Respiratory and anesthesia equipment. Laryngoscopes for tracheal intubation (ISO 7376:2003) | |
UNE-EN ISO 7439:2002 | Contractive intrauterine devices containing copper. Requirements, tests. (ISO 7439:2002) | |
UNE-EN ISO 7886-3:2005 | sterile single-use hypodermic syringes. Part 3: Self-blocking syringes for fixed-dose immunization (ISO 7886-3:2005) | |
UNE-EN ISO 7886-4:2007 | hypodermic syringes Single-use sterile. Part 4: syringes with devices that prevent reuse. (ISO7886-4:2006) | |
UNE-EN ISO 8185:2008 | Respiratory tract humidifiers for medical use. Particular requirements for respiratory humidification systems. (ISO 8185:2007) | |
UNE-EN ISO 8359:1998 | Oxygen concentrators for medical use. Security requirements. (ISO 8359:1996). | |
UNE-EN ISO 8835-2:2008 | Inhalation Anesthesia Systems. Part 2: Systems of anesthesia by respiration. (ISO 8835-2:2007) | |
UNE-EN ISO 8835-3:2008 | Inhalation Anesthesia Systems. Part 3: Systems for the transfer and reception of systems for the evacuation of anesthetic gases. (ISO 8835-3:2007) | |
UNE-EN ISO 8835-4:2005 | Inhalation Anesthesia Systems. Part 4: anesthetic vapor supply devices (ISO 8835-4:2004) | |
UNE-EN ISO 8835-4:2005/AC: 2006 | Inhalation anesthesia systems. Part 4: anesthetic vapor supply devices (ISO 8835-4:2004) | |
UNE-EN ISO 8835-5:2004 | Inhalation anesthesia systems. Part 5: Anesthetic Ventilators (ISO 8835-5:2004) | |
UNE-EN ISO 8835-5:2004/AC: 2006 | Inhalation Anesthesia Systems. Part 5: Anesthetic Ventilators (ISO 8835-5:2004) | |
UNE-EN ISO 8836:2008 | Aspiration probes for use in the airways. (ISO 8836:2007) | |
UNE-EN ISO 9360-1:2000 | Respiratory and anesthesia equipment. Heat and moisture exchangers (ICH) to humidify human-breathed gases. Part 1: ICH for use with minimum breathing volumes of 250 ml. (ISO 9360-1:2000). | |
UNE-EN ISO 9360-2:2003 | Respiratory and anesthesia equipment. Heat and moisture exchangers (ICH) to humidify human-breathed gases. Part 2: ICH for use with tracheostomized patients with minimum breathing volumes of 250 ml. (ISO 9360-2:2001). | |
UNE-EN ISO 9713:2004 | Neurosurgical implants. Self-enclosed clips for intracranial aneurysm. (ISO 9713:2002) | |
UNE-EN ISO 9919:2006 | Electromedical Equipment. Particular requirements for basic safety and essential performance characteristics of pulsioximeters for medical use (ISO 9919:2005) | |
UNE-EN ISO 9919:2006 ERRATUM: 2006 | Electromedical equipment. Particular requirements for basic safety and essential performance characteristics of pulsioximeters for medical use (ISO 9919:2005) | |
UNE-EN ISO 10079-1:2000 |
Aspiration medical equipment. Part 1: Electrical suction equipment. Security requirements. (ISO 10079-1:1999) | |
UNE-EN ISO 10079-2:2000 | Aspiration Medical Equipment. Part 2: Manual aspiration equipment. (ISO 10079-2:1999). | |
UNE-EN ISO 10079-3:2000 | Aspiration Medical Equipment. Part 3: suction equipment fed by a source of vacuum or pressure. (ISO 10079-3:1999). | |
UNE-EN ISO 10555-1/A1:2000 | sterile intravascular catheters for single use. Part 1: General requirements. (ISO 10555-1:1996/A1:1999). | |
UNE-EN ISO 10555-1/A2:2004 | sterile intravascular catheters, for single use. Part 1: General requirements. (ISO 10555-1:1996/AM 2:2004) | |
UNE-EN ISO 10555-1:1997 | sterile intravascular catheters, for single use. Part 1: General requirements. (ISO 10555-1:1995). | |
UNE-EN ISO 10651-2:2005 | Lung respirators for medical use. Particular requirements for basic safety and essential operating characteristics. Part 2: Home-use respirators for dependent patients. (ISO 10651-2:2004) | |
UNE-EN ISO 10651-4:2002 | Lung Respirators. Part 4: Particular requirements for operator-driven resuscitators. (ISO 10651-4:2002) | |
UNE-EN ISO 10651-4:2002/AC: 2006 | Lung Respirators. Part 4: Particular requirements for operator-driven resuscitators. (ISO 10651-4:2002) | |
UNE-EN ISO 10651-6:2005 | Lung respirators for medical use. Particular requirements for basic safety and essential operating characteristics. Part 6: Home respiratory assistance devices (ISO 10651-6:2004) | |
UNE-EN ISO 10993-3:2004 | Biological assessment of products health. Part 3: Genotoxicity assays, carcinogenicity and reproductive toxicity (ISO 10993-3:2003) | |
UNE-EN ISO 10993-4:2003 | Evaluation biological products. Part 4: Selection of trials for blood interactions. (ISO 10993-4:2002) | |
UNE-EN ISO 10993-4:2003/A1:2007 | Biological assessment of medical devices. Part 4: Selection of trials for blood interactions. Modification 1 (ISO 10993-4:2002/Amd 1:2006) | |
UNE-EN ISO 10993-6:2007 | Biological assessment of medical devices. Part 6: Tests relating to local effects after implantation. (ISO 10993-6:2007) | |
UNE-EN ISO 10993-9:2000 | Biological assessment of medical devices. Part 9: Framework for the identification and quantification of potential degradation products. (ISO 10993-9:1999). | |
UNE-EN ISO 10993-10:2003 | Biological assessment of medical devices. Part 10: Tests of irritation and delayed hypersensitivity. (ISO 10993-10:2002) | |
UNE-EN ISO 10993-10:2003/A1:2007 | Biological assessment of medical devices. Part 10: Tests of irritation and delayed hypersensitivity. (ISO 10993-10:2002/Amd 1:2006) | |
UNE-EN ISO 10993-11:2007 | Biological assessment of medical devices. Part 11: Trials of systemic toxicity. (ISO 10993-11:2006) | |
UNE-EN ISO 10993-12:2008 | Biologic assessment of healthcare products. Part 12: Preparation of samples and reference materials. (ISO 10993-12:2007) | |
UNE-EN ISO 10993-13:2000 | Biologic assessment of healthcare products. Part 13: Identification and quantification of the degradation products of polymeric sanitary products. (ISO 10993-13:1998). | |
UNE-EN ISO 10993-14:2002 | Biological assessment of medical devices. Part 14: Identification and quantification of ceramic materials degradation products. (ISO 10993-14:2001) | |
UNE-EN ISO 10993-15:2001 | Biological assessment of medical devices. Part 15: Identification and quantification of metal and alloy degradation products. (ISO 10993-15:2000) | |
UNE-EN ISO 10993-16:1998 | Biological assessment of medical devices. Part 16: Design of the toxicocytic study of degradation products and leaching substances. (ISO 10993-16:1997). | |
UNE-EN ISO 10993-17:2003 | Biological assessment of medical devices. Part 17: Establishment of permissible limits for leachable substances. (ISO 10993-17:2002) | |
UNE-EN ISO 10993-18:2006 | Biological assessment of medical devices. Part 18: Chemical characterization of materials. (ISO 10993-18:2005). | |
UNE-EN ISO 11138-2:2007 | Sterilization of Healthcare Products. Biological indicators. Part 2: Biological indicators for ethylene oxide sterilization processes. (ISO 11138-2:2006) | |
UNE-EN ISO 11138-3:2007 | Sterilization of Healthcare Products. Biological indicators. Part 3: Biological indicators for water vapor sterilization processes. (ISO 11138-3:2006) | |
UNE-EN ISO 11140-1:2006 | Sterilization of Healthcare Products. Chemical indicators. Part 1: General requirements (ISO 11140-1:2005) | |
UNE-EN ISO 11140-3:2007 | sterilisation of medical devices. Chemical indicators. Part 3: Class 2 indicator systems for use in the Bowie and Dick vapor penetration assay. (ISO 11140-3:2007) | |
UNE-EN ISO 11140-3:2007/AC: 2008 | sterilisation of medical devices. Chemical indicators. Part 3: Class 2 indicator systems for use in the Bowie and Dick vapor penetration assay. (ISO 11140-3:2007/Cor 1:2007) | |
UNE-EN ISO 11197:2005 | Medical supply units. (ISO 11197:2004) | |
UNE-EN ISO 11607-1:2007 | Packaging for terminally sterilized sanitary products. Part 1: Requirements for materials, sterile barrier systems and packaging systems. (ISO 11607-1:2006) | |
UNE-EN ISO 11810-1:2006 | lasers and equipment related to lasers. Method of testing and classification for laser resistance of surgical wipes and/or protective covers of the patient. Part 1: Primary Ignition and Penetration. (ISO 11810-1:2005) | |
UNE-EN ISO 11810-2:2008 | lasers and equipment related to lasers. Method of testing and classification for laser resistance of surgical wipes and/or protective covers of patients. Part 2: Secondary Ignition. (ISO 11810-2:2007) | |
UNE-EN ISO 11979-8:2007 | ophthalmic implants. Intraocular lenses. Part 8: Fundamental requirements. (ISO 11979-8:2006) | |
UNE-EN ISO 12870:2005 | ophthalmic Optical. Eyewear mounts. General requirements and test methods. (ISO 12870:2004). | |
UNE-EN ISO 14155-1:2003 | Clinical research of human health products. Part 1: General requirements. (ISO 14155-1:2003) | |
UNE-EN ISO 14155-1:2003 ERRATUM: 2005 | Clinical research of human health products. Part 1: General requirements. (ISO 14155-1:2003) | |
UNE-EN ISO 14155-2:2004 | Clinical research of human health products. Part 2: Clinical research plans (ISO 14155-2:2003) | |
UNE-EN ISO 14408:2006 | tracheal tubes for laser surgery-Requirements for the marking and information accompanying the product (ISO 14408:2005) | |
UNE-EN ISO 14602:1999 | Non-active surgical implants. Implants for osteosynthesis. Special requirements. (ISO 14602:1998). | |
UNE-EN ISO 14607:2007 | Non-active surgical implants. Breast implants. Special requirements. (ISO 14607:2007) | |
UNE-EN ISO 14630:2008 | Non-active surgical implants. General requirements. (ISO 14630:2008) | |
UNE-EN ISO 14889:2004 | ophthalmic Optical. Glasses for glasses. Essential requirements for finished lenses without beveling. (ISO 14889:2003) | |
UNE-EN ISO 14971/AC: 2002 | Healthcare products. Application of risk management to medical devices. (ISO 14971:2000) | |
UNE-EN ISO 14971/A1:2003 | Healthcare products. Application of risk management to medical devices. Modification 1: Requirements Justification (ISO 14971:2000/AM1:2003) | |
UNE-EN ISO 14971:2001 | Healthcare products. Application of risk management to medical devices. (ISO 14971:2000) | |
UNE-EN ISO 14971:2007 | Healthcare products. Application of risk management to medical devices. (ISO 14971:2007) | |
UNE-EN ISO 15004-1:2007 | ophthalmic instruments. Key requirements and test methods. Part 1: General requirements applicable to all ophthalmic instruments (ISO 15004-1:2006) | |
UNE-EN ISO 15883-1:2007 | Washing machines Disinfectants. Part 1: General requirements, definitions and tests. (ISO 15883-1:2006) | |
UNE-EN ISO 15883-2:2007 | Disinfecting Washers. Part 2: Requirements and testing of disinfecting washing machines using thermal disinfection for surgical instruments, anesthesia equipment, bowls, plates, containers, utensils, glass containers, etc. (ISO 15883-2:2006) | |
UNE-EN ISO 15883-3:2007 | Disinfecting Washers. Part 3: Requirements and testing of disinfecting washing machines using thermal disinfection for human waste containers (ISO 15883-3:2006) | |
UNE-EN ISO 15883-4:2008 |
Sanitizer washers. Part 4: Requirements and tests for washing machines designed for the chemical disinfection of termolabile endoscopes. (ISO 15883-4:2008) | |
UNE-EN ISO 17510-1:2008 | Respiratory therapy for sleep apnea. Part 1: Respiratory therapy equipment for sleep apnea. (ISO 17510-1:2007) | |
UNE-EN ISO 17510-2:2008 | Respiratory therapy for sleep apnea. Part 2: Face masks and application accessories. (ISO 17510-2:2007) | |
UNE-EN ISO 18777:2005 | Liquid oxygen transportable systems for medical use. Particular Requirements (ISO 18777:2005) | |
UNE-EN ISO 18778:2005 | Respiratory equipment. Monitors for children. Special requirements. (ISO 18778:2005) | |
UNE-EN ISO 21534:2008 | Non-active surgical implants. Joint replacement implants. Particular Requirements (ISO 21534:2007) | |
UNE-EN ISO 21535:2008 | Non-active surgical implants. Joint replacement implants. Specific requirements for hip joint replacement implants. (ISO 21535:2007) | |
UNE-EN ISO 21536:2008 | Non-active surgical implants. Joint replacement implants. Specific requirements for knee joint replacement implants. (ISO 21536:2007) | |
UNE-EN ISO 21647:2005 | Electromedical Equipment. Particular requirements for the basic safety and essential performance characteristics of the respiratory gas monitors. (ISO 21647:2004) | |
UNE-EN ISO 21647 :2005/AC: 2006 | Electromedical Equipment. Particular requirements for the basic safety and essential performance characteristics of the respiratory gas monitors. (ISO 21647 :2004/Cor.1:2005 | |
UNE-EN ISO 21649:2007 | Non-needle-free injectors for medical use. Requirements and test methods. (ISO 21649:2006) | |
UNE-EN ISO 23328-2:2008 | Respiratory system filters for anesthetic and respiratory use. Part 2: Different aspects of filtration. (ISO 23328-2:2002). | |
UNE-EN ISO 23747:2008 | Respiratory and anesthetic equipment. Spirometers for peak expiratory flow for the evaluation of lung function in spontaneously breathing human beings. (ISO 23747:2007) |