EN ISO 14801:2016
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DENTISTRY - IMPLANTS - DYNAMIC LOADING TEST FOR ENDOSSEOUS DENTAL IMPLANTS (ISO 14801:2016) |
EN 21942-1 : 1991
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DENTAL VOCABULARY - GENERAL AND CLINICAL TERMS |
EN 21942-2 : 1992
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DENTAL VOCABULARY - DENTAL MATERIALS |
EN ISO 22803:2005
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Dentistry - Membrane materials for guided tissue regeneration in oral and maxillofacial surgery - Contents of a technical file (ISO 22803:2004) |
2007/47/EC : 2007 COR 1 2015
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DIRECTIVE 2007/47/EC OF THE EUROPEAN PARLIAMENT AND OF THE COUNCIL OF 5 SEPTEMBER 2007 AMENDING COUNCIL DIRECTIVE 1990/385/EEC ON THE APPROXIMATION OF THE LAWS OF THE MEMBER STATES RELATING TO ACTIVE IMPLANTABLE MEDICAL DEVICES, COUNCIL DIRECTIVE 1993/42/EEC CONCERNING MEDICAL DEVICES AND DIRECTIVE 1998/8/EC CONCERNING THE PLACING OF BIOCIDAL PRODUCTS ON THE MARKET(TEXT WITH EEA RELEVANCE) |
EN ISO 22794:2009
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Dentistry - Implantable materials for bone filling and augmentation in oral and maxillofacial surgery - Contents of a technical file (ISO 22794:2007, corrected version 2009-01-15) |
EN 1641:2009
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Dentistry - Medical devices for dentistry - Materials |
EN ISO 7405:2008/A1:2013
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DENTISTRY - EVALUATION OF BIOCOMPATIBILITY OF MEDICAL DEVICES USED IN DENTISTRY (ISO 7405:2008) |
CEN/TR 12401:2009
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Dentistry - Guidance on the classification of dental devices and accessories |
EN ISO 22442-1:2015
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Medical devices utilizing animal tissues and their derivatives - Part 1: Application of risk management (ISO 22442-1:2015) |
EN 1041:2008+A1:2013
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Information supplied by the manufacturer of medical devices |
ISO 8601:2004
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Data elements and interchange formats Information interchange Representation of dates and times |
EN ISO 11135-1:2007
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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) |
EN ISO 11137-1:2015
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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, including Amd 1:2013) |
EN ISO 14971:2012
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Medical devices - Application of risk management to medical devices (ISO 14971:2007, Corrected version 2007-10-01) |
EN ISO 14155-2:2009
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Clinical investigation of medical devices for human subjects - Part 2: Clinical investigation plans (ISO 14155-2:2003) |
EN ISO 14155-1:2009
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Clinical investigation of medical devices for human subjects - Part 1: General requirements (ISO 14155-1:2003) |
EN 980:2008
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Symbols for use in the labelling of medical devices |
EN ISO 10451:2010
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Dentistry - Contents of technical file for dental implant systems (ISO 10451:2010) |
EN ISO 10993-1:2009/AC:2010
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BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 1: EVALUATION AND TESTING WITHIN A RISK MANAGEMENT PROCESS (ISO 10993-1:2009/COR 1:2010) |