ISO 18113-3:2009
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use
- Standard No.
- ISO 18113-3:2009
- Release Date
- 2009
- Published By
- International Organization for Standardization (ISO)
- Status
- Replace By
- ISO 18113-3:2022
- Latest
- ISO 18113-3:2022
ISO 18113-3:2009 Referenced Document
- IEC 61010-1:2001 Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 1: General requirements
- IEC 61010-2-101:2002 Safety requirements for electrical equipment for measurement, control and laboratory use - Part 2-101: Particular requirements for in vitro diagnostic (IVD) medical equipment
- IEC 61326-2-6:2005 Electrical equipment for measurement, control and laboratory use, control and laboratory use - EMC requirements - Part 2-6: Particular requirements - In-vitro diagnostic (IVD) medical equipment
- IEC 62366:2007 Medical devices - Application of usability engineering to medical devices
- ISO 14971:2007 Medical devices - Application of risk management to medical devices
- ISO 15223-1:2007 Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part 1: General requirements
- ISO 18113-1:2009 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements
ISO 18113-3:2009 history
- 2022 ISO 18113-3:2022 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use
- 2009 ISO 18113-3:2009 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use
