ISO/TS 20993:2006 PDF
Biological evaluation of medical devices — Guidance on a risk-management process
Biological evaluation of medical devices — Guidance on a risk-management process
- Статус документа:
- Отменён
- Формат:
- Электронный (PDF)
- Количество страниц:
- 4
- Дата публикации:
- 26 июля 2006 г.
- Издание:
- ISO TS 20993 edition 1 version 1
- ICS:
- 11.100.20
ISO/TS 20993:2006 describes a process by which a manufacturer can identify the biological hazards associated with medical devices, estimate and evaluate the risks, control these risks and monitor the effectiveness of the control.
Технические детали
- Технический комитет
- ISO/TC 194 - Biological and clinical evaluation of medical devices
- SKU
- ISO/TS 20993:2006