ISO 18113-1:2009 PDF
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements
Название (английский):
ISO 18113-1:2009
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions and general requirements
- Статус документа:
- Отменён
- Формат:
- Электронный (PDF)
- Количество страниц:
- 49
- Дата публикации:
- 9 декабря 2009 г.
- Издание:
- ISO IS 18113 edition 1 version 1
- ICS:
- 11.100.10
Описание (английский):
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.
Технические детали
- Технический комитет
- ISO/TC 212 - Clinical laboratory testing and in vitro diagnostic test systems
- SKU
- ISO 18113-1:2009