-
-
Available Formats
- Availability
- Priced From ( in USD )
-
Available Formats
-
- Secure PDF 🔒
- Immediate download
- $169.28
- Add to Cart
-
- Printed Edition
- Ships in 1-2 business days
- $204.48
- Add to Cart
-
- Printed Edition + PDF
- Immediate download
- $228.90
- Add to Cart
Customers Who Bought This Also Bought
-
ISO 11135:2014
Priced From $250.00 -
DIN 4049-3
Priced From $183.67 -
DIN 58910-1
Priced From $50.14 -
DIN EN 868-10
Priced From $81.64
About This Item
Document History
-
DIN EN ISO 11135
Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014 + Amd.1:2018) (includes Amendment :2019)- Most Recent
-
DIN EN ISO 11135/A1 - DRAFT
Draft Document - Sterilization of health-care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014/DAM 1:2017); German and English version EN ISO 11135:2014/prA1:2017- Historical Version
-
DIN EN ISO 11135
Sterilization of health care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2014)- Historical Version
-
DIN EN ISO 11135 - DRAFT
Draft Document - Sterilization of health care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO/DIS 11135:2012); German version prEN ISO 11135:2012- Historical Version
-
DIN EN ISO 11135 - DRAFT
Draft Document - Sterilization of health care products - Ethylene oxide - Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135:2011); German version prEN ISO 11135:2011- Historical Version
-
DIN EN ISO 11135-1
viewing
Sterilization of health care products - Ethylene oxide - Part 1: Requirements for the development, validation and routine control of a sterilization process for medical devices (ISO 11135-1:2007)- Historical Version