BS EN 556-1:2001 PDF
Sterilization of medical devices. Requirements for medical devices to be designated "STERILE" - Part 1. Requirements for terminally sterilized medical devices
Sterilization of medical devices. Requirements for medical devices to be designated "STERILE" - Part 1. Requirements for terminally sterilized medical devices
- Статус документа:
- Отменён
- Формат:
- Электронный (PDF)
- Дата публикации:
- 11 декабря 2001 г.
- ICS:
- 11.080.01
- SKU:
- BS EN 556-1:2001
Abstract
BS EN 556-1:2001 Sterilization of medical devices. Requirements for medical devices to be designated "STERILE". Requirements for terminally sterilized medical devices BS EN 556-1 is the standard that specifies the requirements for a terminally sterilized medical device to be designated “STERILE”. BS EN 556-2 specifies the requirements for an aseptically processed medical device to be designated “STERILE”. Designation of a medical device as “STERILE” is only permissible when a validated sterilization process has been applied. Also available for sterilization of medical devices: BS EN 556-2:2015 Sterilization of medical devices. Requirements for medical devices to be designated "STERILE". Requirements for aseptically processed medical devices
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