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UNE-EN ISO 18113-1
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)
Edition
2012-02-22
UNE-EN ISO 18113-2
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)
Edition
2012-02-22
UNE-EN ISO 18113-3
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009)
Edition
2012-02-22
UNE-EN ISO 18113-4
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009)
Edition
2012-02-22
UNE-EN ISO 18113-5
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)
Edition
2012-02-22
UNE-EN ISO 19001
In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology (ISO 19001:2013)
Edition
2013-11-27
UNE-EN ISO 20417
Medical devices - Information to be supplied by the manufacturer (ISO 20417:2021)
Edition
2021-12-07
UNE-EN 818-6+A1
Short link chain for lifting purposes - Safety - Part 6: Chain slings - Specification for information for use and maintenance to be provided by the manufacturer
Edition
2008-07-30
UNE-EN 3475-703
Aerospace series. Cables, electrical, aircraft use. Test methods. Part 703; Permanence of manufacturer´s marking (Endorsed by AENOR in April of 2002.)
Edition
2002-04-01
UNE-EN 3745-703
Aerospace series - Fibres and cables, optical, aircraft use - Test methods - Part 703: Durability of manufacturer's marking (Endorsed by AENOR in March of 2006.)
Edition
2006-03-01