ISO 18113-1:2009 PDF
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements
Open preview (PDF)In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirementsTitle (English):
ISO 18113-1:2009
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements
- Document status:
- Withdrawn
- Format:
- Electronic (PDF)
- Number of pages:
- 49
- Publication date:
- December 9, 2009
- Edition:
- ISO IS 18113 edition 1 version 1
- ICS:
- 11.100.10
Description (English):
ISO 18113-1:2009 defines concepts, establishes general principles and specifies essential requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) medical devices.
Technical details
- Technical committee
- ISO/TC 212 - Clinical laboratory testing and in vitro diagnostic test systems
- SKU
- ISO 18113-1:2009
