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MDD協(xié)調(diào)標(biāo)準(zhǔn)清單

ESO	Reference and title of the harmonised standard (and reference document)	First publication OJ	Reference of superseded standard	Date of cessation of presumption of conformity of superseded standard
CEN	EN 285:2006+A2:2009 Sterilization - Steam sterilizers - Large sterilizers	02/12/2009	EN 285:2006+A1:2008	Date expired (21/03/2010)
CEN	EN 455-1:2000 Medical gloves for single use - Part 1: Requirements and testing for freedom from holes	30/09/2005	EN 455-1:1993	Date expired (30/04/2001)
CEN	EN 455-3:2006 Medical gloves for single use - Part 3: Requirements and testing for biological evaluation	09/08/2007	EN 455-3:1999	Date expired (30/06/2007)
CEN	EN 455-4:2009 Medical gloves for single use - Part 4: Requirements and testing for shelf life determination	07/07/2010
CEN	EN 556-1:2001 Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 1: Requirements for terminally sterilized medical devices	31/07/2002	EN 556:1994 + A1:1998	Date expired (30/04/2002)
CEN	EN 556-1:2001/AC:2006	15/11/2006
CEN	EN 556-2:2003 Sterilization of medical devices - Requirements for medical devices to be designated "STERILE" - Part 2: Requirements for aseptically processed medical devices	09/08/2007
CEN	EN 794-3:1998+A2:2009 Lung ventilators - Part 3: Particular requirements for emergency and transport ventilators	07/07/2010	EN 794-3:1998	Date expired (21/03/2010)
CEN	EN 1041:2008 Information supplied by the manufacturer of medical devices	19/02/2009	EN 1041:1998	Date expired (31/08/2011)
CEN	EN 1060-3:1997+A2:2009 Non-invasive sphygmomanometers - Part 3: Supplementary requirements for electro-mechanical blood pressure measuring systems	07/07/2010	EN 1060-3:1997	Date expired (31/05/2010)
CEN	EN 1060-4:2004 Non-invasive sphygmomanometers - Part 4: Test procedures to determine the overall system accuracy of automated non-invasive sphygmomanometers	30/09/2005
CEN	EN 1282-2:2005+A1:2009 Tracheostomy tubes - Part 2: Paediatric tubes (ISO 5366-3:2001, modified)	07/07/2010	EN 1282-2:2005	Date expired (21/03/2010)
CEN	EN 1422:1997+A1:2009 Sterilizers for medical purposes - Ethylene oxide sterilizers - Requirements and test methods	02/12/2009	EN 1422:1997	Date expired (21/03/2010)
CEN	EN 1618:1997 Catheters other than intravascular catheters - Test methods for common properties	09/05/1998
CEN	EN 1639:2009 Dentistry - Medical devices for dentistry - Instruments	07/07/2010	EN 1639:2004	Date expired (30/04/2010)
CEN	EN 1640:2009 Dentistry - Medical devices for dentistry - Equipment	07/07/2010	EN 1640:2004	Date expired (30/04/2010)
CEN	EN 1641:2009 Dentistry - Medical devices for dentistry - Materials	07/07/2010	EN 1641:2004	Date expired (30/04/2010)
CEN	EN 1642:2011 Dentistry - Medical devices for dentistry - Dental implants	27/04/2012	EN 1642:2009	Date expired (30/04/2012)
CEN	EN 1707:1996 Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment - Lock fittings	17/05/1997
CEN	EN 1782:1998+A1:2009 Tracheal tubes and connectors	07/07/2010	EN 1782:1998	Date expired (21/03/2010)
CEN	EN 1789:2007+A1:2010 Medical vehicles and their equipment - Road ambulances	18/01/2011
CEN	EN 1820:2005+A1:2009 Anaesthetic reservoir bags (ISO 5362:2000, modified)	07/07/2010	EN 1820:2005	Date expired (21/03/2010)
CEN	EN 1865-3:2012 Patient handling equipment used in road ambulances - Part 3: Heavy duty stretcher	30/08/2012	EN 1865:1999	31/12/2012
CEN	EN 1865-4:2012 Patient handling equipment used in road ambulances - Part 4: Foldable patient transfer chair	30/08/2012	EN 1865:1999	Date expired (31/10/2012)
CEN	EN 1865-5:2012 Patient handling equipment used in road ambulances - Part 5: Stretcher support	30/08/2012	EN 1865:1999	31/12/2012
CEN	EN 1985:1998 Walking aids - General requirements and test methods	10/08/1999
This standard still needs to be amended to take into account the requirements introduced by Directive 2007/47/EC. The amended standard will be published by CEN as soon as possible. Manufacturers are advised to check whether all relevant Essential Requirements of the amended directive are appropriately covered.
CEN	EN ISO 3826-2:2008 Plastics collapsible containers for human blood and blood components - Part 2: Graphical symbols for use on labels and instruction leaflets (ISO 3826-2:2008)	19/02/2009
CEN	EN ISO 3826-3:2007 Plastics collapsible containers for human blood and blood components - Part 3: Blood bag systems with integrated features (ISO 3826-3:2006)	27/02/2008
CEN	EN ISO 4074:2002 Natural latex rubber condoms - Requirements and test methods (ISO 4074:2002)	31/07/2002	EN 600:1996	Date expired (31/08/2005)
CEN	EN ISO 4074:2002/AC:2008	02/12/2009
CEN	EN ISO 4135:2001 Anaesthetic and respiratory equipment - Vocabulary (ISO 4135:2001)	31/07/2002	EN ISO 4135:1996	Date expired (28/02/2002)
CEN	EN ISO 5356-1:2004 Anaesthetic and respiratory equipment - Conical connectors - Part 1: Cones and sockets (ISO 5356-1:2004)	30/09/2005	EN 1281-1:1997	Date expired (30/11/2004)
CEN	EN ISO 5356-2:2007 Anaesthetic and respiratory equipment - Conical connectors - Part 2: Screw-threaded weight-bearing connectors (ISO 5356-2:2006)	09/11/2007	EN 1281-2:1995	Date expired (29/02/2008)
CEN	EN ISO 5359:2008 Low-pressure hose assemblies for use with medical gases (ISO 5359:2008)	23/07/2008	EN 739:1998	Date expired (30/06/2010)
CEN	EN ISO 5359:2008/A1:2011	30/08/2012		Date expired (30/06/2012)
CEN	EN ISO 5360:2009 Anaesthetic vaporizers - Agent-specific filling systems (ISO 5360:2006)	02/12/2009	EN ISO 5360:2007	Date expired (21/03/2010)
CEN	EN ISO 5366-1:2009 Anaesthetic and respiratory equipment - Tracheostomy tubes - Part 1: Tubes and connectors for use in adults (ISO 5366-1:2000)	02/12/2009	EN ISO 5366-1:2004	Date expired (21/03/2010)
CEN	EN ISO 5840:2009 Cardiovascular implants - Cardiac valve prostheses (ISO 5840:2005)	02/12/2009	EN ISO 5840:2005	Date expired (21/03/2010)
CEN	EN ISO 7197:2009 Neurosurgical implants - Sterile, single-use hydrocephalus shunts and components (ISO 7197:2006, including Cor 1:2007)	02/12/2009	EN ISO 7197:2006	Date expired (21/03/2010)
CEN	EN ISO 7376:2009 Anaesthetic and respiratory equipment - Laryngoscopes for tracheal intubation (ISO 7376:2009)	02/12/2009	EN ISO 7376:2009	Date expired (21/03/2010)
CEN	EN ISO 7396-1:2007 Medical gas pipeline systems - Part 1: Pipeline systems for compressed medical gases and vacuum (ISO 7396-1:2007)	09/08/2007	EN 737-3:1998	Date expired (30/04/2009)
	EN ISO 7396-1:2007/A1:2010	07/07/2010		Date expired (31/07/2010)
	EN ISO 7396-1:2007/A2:2010	07/07/2010		Date expired (31/08/2010)
CEN	EN ISO 7396-2:2007 Medical gas pipeline systems - Part 2: Anaesthetic gas scavenging disposal systems (ISO 7396-2:2007)	09/08/2007	EN 737-2:1998	Date expired (30/04/2009)
CEN	EN ISO 7886-3:2009 Sterile hypodermic syringes for single use - Part 3: Auto-disable syringes for fixed-dose immunization (ISO 7886-3:2005)	07/07/2010	EN ISO 7886-3:2005	Date expired (21/03/2010)
CEN	EN ISO 7886-4:2009 Sterile hypodermic syringes for single use - Part 4: Syringes with re-use prevention feature (ISO 7886-4:2006)	07/07/2010	EN ISO 7886-4:2006	Date expired (21/03/2010)

MDD協(xié)調(diào)標(biāo)準(zhǔn)清單（2）

CEN	EN ISO 8185:2009 Respiratory tract humidifiers for medical use - Particular requirements for respiratory humidification systems (ISO 8185:2007)	02/12/2009	EN ISO 8185:2007	Date expired (21/03/2010)
CEN	EN ISO 8359:2009 Oxygen concentrators for medical use - Safety requirements (ISO 8359:1996)	02/12/2009	EN ISO 8359:1996	Date expired (21/03/2010)
CEN	EN ISO 8835-2:2009 Inhalational anaesthesia systems - Part 2: Anaesthetic breathing systems (ISO 8835-2:2007)	02/12/2009	EN ISO 8835-2:2007	Date expired (21/03/2010)
CEN	EN ISO 8835-3:2009 Inhalational anaesthesia systems - Part 3: Transfer and receiving systems of active anaesthetic gas scavenging systems (ISO 8835-3:2007)	02/12/2009	EN ISO 8835-3:2007	Date expired (21/03/2010)
CEN	EN ISO 8835-3:2009/A1:2010	13/05/2011		Date expired (30/04/2011)
CEN	EN ISO 8835-4:2009 Inhalational anaesthesia systems - Part 4: Anaesthetic vapour delivery devices (ISO 8835-4:2004)	02/12/2009	EN ISO 8835-4:2004	Date expired (21/03/2010)
CEN	EN ISO 8835-5:2009 Inhalational anaesthesia systems - Part 5: Anaesthetic ventilators (ISO 8835-5:2004)	02/12/2009	EN ISO 8835-5:2004	Date expired (21/03/2010)
CEN	EN ISO 9170-1:2008 Terminal units for medical gas pipeline systems - Part 1: Terminal units for use with compressed medical gases and vacuum (ISO 9170-1:2008)	19/02/2009	EN 737-1:1998	Date expired (31/07/2010)
CEN	EN ISO 9170-2:2008 Terminal units for medical gas pipeline systems - Part 2: Terminal units for anaesthetic gas scavenging systems (ISO 9170-2:2008)	19/02/2009	EN 737-4:1998	Date expired (31/07/2010)
CEN	EN ISO 9360-1:2009 Anaesthetic and respiratory equipment - Heat and moisture exchangers (HMEs) for humidifying respired gases in humans - Part 1: HMEs for use with minimum tidal volumes of 250 ml (ISO 9360-1:2000)	02/12/2009	EN ISO 9360-1:2000	Date expired (21/03/2010)
CEN	EN ISO 9360-2:2009 Anaesthetic and respiratory equipment - Heat and moisture exchangers (HMEs) for humidifying respired gases in humans - Part 2: HMEs for use with tracheostomized patients having minimum tidal volumes of 250 ml (ISO 9360-2:2001)	02/12/2009	EN ISO 9360-2:2002	Date expired (21/03/2010)
CEN	EN ISO 9713:2009 Neurosurgical implants - Self-closing intracranial aneurysm clips (ISO 9713:2002)	02/12/2009	EN ISO 9713:2004	Date expired (21/03/2010)
CEN	EN ISO 10079-1:2009 Medical suction equipment - Part 1: Electrically powered suction equipment - Safety requirements (ISO 10079-1:1999)	02/12/2009	EN ISO 10079-1:1999	Date expired (21/03/2010)
CEN	EN ISO 10079-2:2009 Medical suction equipment - Part 2: Manually powered suction equipment (ISO 10079-2:1999)	02/12/2009	EN ISO 10079-2:1999	Date expired (21/03/2010)
CEN	EN ISO 10079-3:2009 Medical suction equipment - Part 3: Suction equipment powered from a vacuum or pressure source (ISO 10079-3:1999)	02/12/2009	EN ISO 10079-3:1999	Date expired (21/03/2010)
CEN	EN ISO 10328:2006 Prosthetics - Structural testing of lower-limb prostheses - Requirements and test methods (ISO 10328:2006)	09/08/2007
This standard still needs to be amended to take into account the requirements introduced by Directive 2007/47/EC. The amended standard will be published by CEN as soon as possible. Manufacturers are advised to check whether all relevant Essential Requirements of the amended directive are appropriately covered.
CEN	EN ISO 10524-1:2006 Pressure regulators for use with medical gases - Part 1: Pressure regulators and pressure regulators with flow-metering devices (ISO 10524-1:2006)	02/06/2006	EN 738-1:1997	Date expired (31/10/2008)
CEN	EN ISO 10524-2:2006 Pressure regulators for use with medical gases - Part 2: Manifold and line pressure regulators (ISO 10524-2:2005)	07/06/2009	EN 738-2:1998	Date expired (31/10/2008)
CEN	EN ISO 10524-3:2006 Pressure regulators for use with medical gases - Part 3: Pressure regulators integrated with cylinder valves (ISO 10524-3:2005)	07/09/2006	EN 738-3:1998	Date expired (31/10/2008)
CEN	EN ISO 10524-4:2008 Pressure regulators for use with medical gases - Part 4: Low-pressure regulators (ISO 10524-4:2008)	23/07/2008	EN 738-4:1998	Date expired (30/06/2010)
CEN	EN ISO 10535:2006 Hoists for the transfer of disabled persons - Requirements and test methods (ISO 10535:2006)	09/08/2007	EN ISO 10535:1998	Date expired (30/06/2007)
This standard still needs to be amended to take into account the requirements introduced by Directive 2007/47/EC. The amended standard will be published by CEN as soon as possible. Manufacturers are advised to check whether all relevant Essential Requirements of the amended directive are appropriately covered.
CEN	EN ISO 10555-1:2009 Sterile, single-use intravascular catheters - Part 1: General requirements (ISO 10555-1:1995, including Amd 1:1999 and Amd 2:2004)	02/12/2009	EN ISO 10555-1:1996	Date expired (21/03/2010)
CEN	EN ISO 10651-2:2009 Lung ventilators for medical use - Particular requirements for basic safety and essential performance - Part 2: Home care ventilators for ventilator-dependent patients (ISO 10651-2:2004)	02/12/2009	EN ISO 10651-2:2004	Date expired (21/03/2010)
CEN	EN ISO 10651-4:2009 Lung ventilators - Part 4: Particular requirements for operator-powered resuscitators (ISO 10651-4:2002)	02/12/2009	EN ISO 10651-4:2002	Date expired (21/03/2010)
CEN	EN ISO 10651-6:2009 Lung ventilators for medical use - Particular requirements for basic safety and essential performance - Part 6: Home-care ventilatory support devices (ISO 10651-6:2004)	02/12/2009	EN ISO 10651-6:2004	Date expired (21/03/2010)
CEN	EN ISO 10993-1:2009 Biological evaluation of medical devices - Part 1: Evaluation and testing within a risk management process (ISO 10993-1:2009)	02/12/2009	EN ISO 10993-1:2009	Date expired (21/03/2010)
CEN	EN ISO 10993-1:2009/AC:2010	18/01/2011
CEN	EN ISO 10993-3:2009 Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity (ISO 10993-3:2003)	02/12/2009	EN ISO 10993-3:2003	Date expired (21/03/2010)
CEN	EN ISO 10993-4:2009 Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002, including Amd 1:2006)	02/12/2009	EN ISO 10993-4:2002	Date expired (21/03/2010)
CEN	EN ISO 10993-5:2009 Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:2009)	02/12/2009	EN ISO 10993-5:1999	Date expired (31/12/2009)
CEN	EN ISO 10993-6:2009 Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007)	02/12/2009	EN ISO 10993-6:2007	Date expired (21/03/2010)
CEN	EN ISO 10993-7:2008 Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008)	19/02/2009
CEN	EN ISO 10993-7:2008/AC:2009	07/07/2010
CEN	EN ISO 10993-9:2009 Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products (ISO 10993-9:2009)	02/12/2009	EN ISO 10993-9:2009	Date expired (21/03/2010)
CEN	EN ISO 10993-11:2009 Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2006)	02/12/2009	EN ISO 10993-11:2006	Date expired (21/03/2010)
CEN	EN ISO 10993-12:2012 (new) Biological evaluation of medical devices - Part 12: Sample preparation and reference materials (ISO 10993-12:2012)	This is the first publication	EN ISO 10993-12:2009	31/01/2013
CEN	EN ISO 10993-13:2010 Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices (ISO 10993-13:2010)	18/01/2011	EN ISO 10993-13:2009	Date expired (31/12/2010)
CEN	EN ISO 10993-14:2009 Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics (ISO 10993-14:2001)	02/12/2009	EN ISO 10993-14:2001	Date expired (21/03/2010)

MDD協(xié)調(diào)標(biāo)準(zhǔn)清單（3）

CEN	EN ISO 10993-15:2009 Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys (ISO 10993-15:2000)	02/12/2009	EN ISO 10993-15:2000	Date expired (21/03/2010)
CEN	EN ISO 10993-16:2010 Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables (ISO 10993-16:2010)	07/07/2010	EN ISO 10993-16:2009	Date expired (31/08/2010)
CEN	EN ISO 10993-17:2009 Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances (ISO 10993-17:2002)	02/12/2009	EN ISO 10993-17:2002	Date expired (21/03/2010)
CEN	EN ISO 10993-18:2009 Biological evaluation of medical devices - Part 18: Chemical characterization of materials (ISO 10993-18:2005)	02/12/2009	EN ISO 10993-18:2005	Date expired (21/03/2010)
CEN	EN ISO 11135-1:2007 Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11135-1:2007)	09/08/2007	EN 550:1994	Date expired (31/05/2010)
CEN	EN ISO 11137-1:2006 Sterilization of health care products - Radiation - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11137-1:2006)	07/09/2006	EN 552:1994	Date expired (30/04/2009)
CEN	EN ISO 11137-2:2012 Sterilization of health care products - Radiation - Part 2: Establishing the sterilization dose (ISO 11137-2:2012)	30/08/2012	EN ISO 11137-2:2007	Date expired (30/09/2012)
CEN	EN ISO 11138-2:2009 Sterilization of health care products - Biological indicators - Part 2: Biological indicators for ethylene oxide sterilization processes (ISO 11138-2:2006)	02/12/2009	EN ISO 11138-2:2006	Date expired (21/03/2010)
CEN	EN ISO 11138-3:2009 Sterilization of health care products - Biological indicators - Part 3: Biological indicators for moist heat sterilization processes (ISO 11138-3:2006)	02/12/2009	EN ISO 11138-3:2006	Date expired (21/03/2010)
CEN	EN ISO 11140-1:2009 Sterilization of health care products - Chemical indicators - Part 1: General requirements (ISO 11140-1:2005)	02/12/2009	EN ISO 11140-1:2005	Date expired (21/03/2010)
CEN	EN ISO 11140-3:2009 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, including Cor 1:2007)	02/12/2009	EN ISO 11140-3:2007	Date expired (21/03/2010)
CEN	EN ISO 11197:2009 Medical supply units (ISO 11197:2004)	02/12/2009	EN ISO 11197:2004	Date expired (21/03/2010)
CEN	EN ISO 11607-1:2009 Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2006)	02/12/2009	EN ISO 11607-1:2006	Date expired (21/03/2010)
CEN	EN ISO 11607-2:2006 Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006)	07/09/2006
CEN	EN ISO 11737-1:2006 Sterilization of medical devices - Microbiological methods - Part 1: Determination of a population of microorganisms on products (ISO 11737-1:2006)	07/09/2006	EN 1174-2:1996 EN 1174-1:1996 EN 1174-3:1996	Date expired (31/10/2006)
CEN	EN ISO 11737-1:2006/AC:2009	02/12/2009
CEN	EN ISO 11737-2:2009 Sterilization of medical devices - Microbiological methods - Part 2: Tests of sterility performed in the definition, validation and maintenance of a sterilization process (ISO 11737-2:2009)	07/07/2010
CEN	EN ISO 11810-1:2009 Lasers and laser-related equipment - Test method and classification for the laser resistance of surgical drapes and/or patient protective covers - Part 1: Primary ignition and penetration (ISO 11810-1:2005)	02/12/2009
CEN	EN ISO 11810-2:2009 Lasers and laser-related equipment - Test method and classification for the laser-resistance of surgical drapes and/or patient-protective covers - Part 2: Secondary ignition (ISO 11810-2:2007)	02/12/2009	EN ISO 11810-2:2007	Date expired (21/03/2010)
CEN	EN ISO 11979-8:2009 Ophthalmic implants - Intraocular lenses - Part 8: Fundamental requirements (ISO 11979-8:2006)	02/12/2009	EN ISO 11979-8:2006	Date expired (21/03/2010)
CEN	EN 12006-2:1998+A1:2009 Non active surgical implants - Particular requirements for cardiac and vascular implants - Part 2: Vascular prostheses including cardiac valve conduits	02/12/2009	EN 12006-2:1998	Date expired (21/03/2010)
CEN	EN 12183:2009 Manual wheelchairs - Requirements and test methods	07/07/2010
CEN	EN 12184:2009 Electrically powered wheelchairs, scooters and their chargers - Requirements and test methods	07/07/2010
CEN	EN 12342:1998+A1:2009 Breathing tubes intended for use with anaesthetic apparatus and ventilators	07/07/2010	EN 12342:1998	Date expired (21/03/2010)
CEN	EN 12470-1:2000+A1:2009 Clinical thermometers - Part 1: Metallic liquid-in-glass thermometers with maximum device	02/12/2009	EN 12470-1:2000	Date expired (21/03/2010)
CEN	EN 12470-2:2000+A1:2009 Clinical thermometers - Part 2: Phase change type (dot matrix) thermometers	02/12/2009	EN 12470-2:2000	Date expired (21/03/2010)
CEN	EN 12470-3:2000+A1:2009 Clinical thermometers - Part 3: Performance of compact electrical thermometers (non-predictive and predictive) with maximum device	02/12/2009	EN 12470-3:2000	Date expired (21/03/2010)
CEN	EN 12470-4:2000+A1:2009 Clinical thermometers - Part 4: Performance of electrical thermometers for continuous measurement	02/12/2009	< 更多收起服務(wù)流程官方收費(fèi) 基礎(chǔ)法規(guī) 時(shí)間分布相關(guān)服務(wù) 服務(wù)流程資料添加中.... 官方收費(fèi)資料添加中.... 基礎(chǔ)法規(guī)資料添加中.... 相關(guān)服務(wù)資料添加中.... 醫(yī)療器械歐盟CE認(rèn)證協(xié)調(diào)標(biāo)準(zhǔn)清單 CB體系醫(yī)療器械電氣設(shè)備標(biāo)準(zhǔn) 醫(yī)療器械認(rèn)證技術(shù)文件資料清單醫(yī)療器械歐盟CE認(rèn)證格慧泰福歐盟醫(yī)療器械MDR認(rèn)證（CE認(rèn)證）技術(shù)服務(wù) MDD產(chǎn)品分類(lèi) 醫(yī)療器械MDR認(rèn)證（CE認(rèn)證）咨詢(xún)服務(wù)概述歐盟CE服務(wù)簡(jiǎn)介全國(guó)服務(wù)熱線(xiàn)： 400-9905-168 關(guān)注我們關(guān)于我們公司簡(jiǎn)介加入我們聯(lián)系我們信息中心不良事件信息通報(bào) 全國(guó)醫(yī)械辦事指南行業(yè)展會(huì)信息發(fā)布信息報(bào)道我們的服務(wù) 醫(yī)療器械注冊(cè) 化妝品體外診斷試劑注冊(cè) 醫(yī)藥包裝服務(wù) 網(wǎng)站地圖丨收藏本站丨免責(zé)聲明丨聯(lián)系我們粵ICP備13059948號(hào) 廣州格慧泰福（GHTF）生物科技有限公司版權(quán)所有 ?? 感谢您访问我们的网站，您可能还对以下资源感兴趣：中文无码精品A∨

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