Development Note
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Indice de classement: S95-186-2-56. PR NF EN ISO 80601-2-56 June 2012. (06/2012) Supersedes NF EN 12470-3, NF EN 12470-4 & NF EN 12470-5. (01/2017) 2012 version is still active. (11/2017) |
Document Type
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Standard |
ISBN
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Pages
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Product Note
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NEW CHILD AMD 1 2020 IS NOW ADDED |
Published
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Publisher
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Association Francaise de Normalisation
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Status
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Current |
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) |
ISO 14937:2009
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Sterilization of health care products General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices |
ISO 14155:2011
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Clinical investigation of medical devices for human subjects Good clinical practice |
ISO 15223-1:2016
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Medical devices Symbols to be used with medical device labels, labelling and information to be supplied Part 1: General requirements |
ISO 17664:2017
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Processing of health care products Information to be provided by the medical device manufacturer for the processing of medical devices |
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