11.100.10: In vitro diagnostic test systems
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UNE-EN ISO 18113-1:2010
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)
standard by UNE-EN ISO, 06/23/2010.
Languages:
- MULTI-USER
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UNE-EN ISO 18113-2:2010
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)
standard by UNE-EN ISO, 06/16/2010.
Languages:
- MULTI-USER
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UNE-EN ISO 18113-3:2010
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009)
standard by UNE-EN ISO, 07/07/2010.
Languages:
- MULTI-USER
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UNE-EN ISO 18113-4:2010
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2009)
standard by UNE-EN ISO, 07/07/2010.
Languages:
- MULTI-USER
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UNE-EN ISO 18113-5:2010
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)
standard by UNE-EN ISO, 06/09/2010.
Languages:
- MULTI-USER
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UNE-EN 591:2001
Instructions for use for in vitro diagnostic instruments for professional use.
standard by UNE-EN, 10/19/2001.
Languages:
- MULTI-USER
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UNE-EN 592:2002
Instructions for use for in vitro diagnostic instruments for self-testing.
standard by UNE-EN, 06/28/2002.
Languages:
- MULTI-USER
