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ISO 18113-1:2022 Edition 10/2022
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements
TC/SC : ISO/TC 212/WG 3
Status : Standard  -  Active
  •  
  • 171.3
  •  

ISO 17593:2022 Edition 03/2022
Clinical laboratory testing and in vitro medical devices — Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy
TC/SC : ISO/TC 212/WG 3
Status : Standard  -  Active
  •  
  • 171.3
  •  

ISO 18113-2:2022 Edition 10/2022
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional use
TC/SC : ISO/TC 212/WG 3
Status : Standard  -  Active
  •  
  • 55.6
  •  

ISO 18113-4:2022 Edition 10/2022
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testing
TC/SC : ISO/TC 212/WG 3
Status : Standard  -  Active
  •  
  • 55.6
  •  

ISO 18113-5:2022 Edition 10/2022
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testing
TC/SC : ISO/TC 212/WG 3
Status : Standard  -  Active
  •  
  • 55.6
  •  

ISO 18113-3:2022 Edition 10/2022
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use
TC/SC : ISO/TC 212/WG 3
Status : Standard  -  Active
  •  
  • 55.6
  •  

 

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