| 1. |
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AFNOR NF EN ISO 11135-1 |
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2007-AUG-01 • 现用 •
Sterilization of health care products - Ethylene oxide - Part 1 : requirements for development, validation and routine control of a sterilization process for medical devices
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| 2. |
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BSI BS EN ISO 11135-1 |
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2007-JUN-29 • 现用 •
Sterilization of health care products — Ethylene oxide — Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
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| 3. |
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CEN EN ISO 11135-1 |
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2007-MAY-01 • 现用 •
Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
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| 4. |
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DIN DIN EN ISO 11135-1 |
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2007-AUG-01 • 现用 •
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); German version EN ISO 11135-1:2007
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| 5. |
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DIN DIN EN ISO 11135-1 |
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2007-AUG-01 • 现用 •
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)
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| 6. |
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DS DS/EN ISO 11135-1 |
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2007-JUN-14 • 现用 •
Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
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| 7. |
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ISO 11135-1 |
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2007-MAY-01 • 现用 •
Sterilization of health care products — Ethylene oxide — Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices-First Edition
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| 8. |
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SN NS-EN ISO 11135-1:2007 |
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2007-SEP-01 • 现用 •
Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices (ISO 11135-1:2007)
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| 9. |
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UNI UNI EN ISO 11135-1 |
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2008-JAN-24 • 现用 •
Sterilization of health care products - Ethylene oxide - Part 1: Requirements for development, validation and routine control of a sterilization process for medical devices
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