Committee
|
CTN 111 |
Development Note
|
Supersedes UNE EN 980. (07/2015) |
Document Type
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Standard |
ISBN
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|
Pages
|
|
Published
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|
Publisher
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Asociacion Espanola de Normalizacion
|
Status
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Superseded |
Superseded By
|
|
Supersedes
|
|
ISO 7010:2011
|
Graphical symbols Safety colours and safety signs Registered safety signs |
ISO 15223-2:2010
|
Medical devices — Symbols to be used with medical device labels, labelling, and information to be supplied — Part 2: Symbol development, selection and validation |
ISO 18113-1:2009
|
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements |
ISO 18113-4:2009
|
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testing |
EN 1041:2008+A1:2013
|
Information supplied by the manufacturer of medical devices |
ISO 8601:2004
|
Data elements and interchange formats Information interchange Representation of dates and times |
IEC 80416-3:2002+AMD1:2011 CSV
|
Basic principles for graphical symbols for use on equipment - Part 3: Guidelines for the application of graphical symbols |
IEC 80416-1:2008
|
Basic principles for graphical symbols for use on equipment - Part 1: Creation of graphical symbols for registration |
ISO 18113-2:2009
|
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional use |
ISO 3864-1:2011
|
Graphical symbols Safety colours and safety signs Part 1: Design principles for safety signs and safety markings |
ISO 14971:2007
|
Medical devices Application of risk management to medical devices |
ISO 7000:2014
|
Graphical symbols for use on equipment Registered symbols |
ISO 18113-5:2009
|
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testing |
ISO 18113-3:2009
|
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use |
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