Medical Device Documents collection

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ANSI/AAMI/ISO 11607-2:2006 Identical : ISO 11737-1: 2006 ANSI/AAMI/ISO 11737-1:2006 : Identical ISO 11737-2:2009 : ANSI/AAMI/ISO 11737-2:2009 Identical

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ISO 11607-2:2006 ANSI/AAMI/ISO 11607-2:2006 Identical ISO 11737-1: 2006 ANSI/AAMI/ISO 11737-1:2006 Identical ISO 11737-2:1998 ANSI/AAMI/ISO 11737-2:1998 Identical

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ISO 11607-2:2006 Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and embly processes. ISO 11737-1:2006 &

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Reference number ISO 11737-1:2006(E) © ISO 2006 INTERNATIONAL STANDARD ISO 11737-1 Second edition 2006-04-01 Sterilization of medical devices — Microbiological ...

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ANSI/AAMI/ISO 11607-2:2006 : Identical : ISO 11737-1: 2006 : ANSI/AAMI/ISO 11737-1:2006 : Identical : ISO 11737-2:2009 : ANSI/AAMI/ISO 11737-2:2009 : Identical

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en iso 11737-1:2006/ac:2009 en iso 11737-2:2009 en 1422:1997+a1:2009 en iso 14161:2009 en iso 11138-2:2009 en iso 14937:2009 en iso 11607-1:2009

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ANSI/AAMI/ISO 11737-1:2006 Sterilization of medical devices—Microbiological methods, Part 2: Tests of sterility performed in the validation of a sterilization process,

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ISO/CD 2006-2 Rubber latex, synthetic – Determination of mechanical stability ... ISO/CD 11737-2 Sterilization of medical devices – Microbiological methods – Part 2 ...

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(31.10.2006) EN ISO 11737-1:2006/AC:2009 2.12.2009 CEN EN ISO 11737-2:2009 Sterilization of medical devices - Microbiological methods - Part 2:

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EN ISO 11607-1:2006 Note 2.1 21.3.2010 CEN EN ISO 11737-1:2006 Sterilisation of medical devices — Microbiological methods — Part 1: Determination of a population of

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... medical devices 23.7.2008 EN 980:2003 Note 2.1 Date expired (31.5.2010) CEN EN ISO 11737-2 ... medical equipment IEC 61010-2-101:2002 (Modified) 17.12.2002 Cenelec EN 61326-2-6:2006 ...

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ISO 11137-2: 2006 - Sterilization of health care products – Radiation – Part 2: Establishing the sterilization dose ISO 11737-1: 2006 – Sterilization of ...

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AAMI/ANSI/ISO 11737-1: 2006. Sterilization of Medical devices-Microbiological methods-Part 1: Estimation of the population of microorganisms on product

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2: Guidance BS EN 1174-2:1997 Replaced by BS EN ISO 11737-1:2006 CEN EN 1174-3:1996 OJ97/C149/05 OJ2005/C153/20 OJ2006/C129/02 Sterilisation of medical

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2.09(3) 6 EN ISO 11737 – 1:2006 : Sterilization of medical devices – Microbiological methods – Part 1: Determination of a population of microrganisms on products

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BS EN ISO 11737-1:2006 CEN EN ISO 11737-2:2009 OJ2010/C183/02 Sterilization of medical devices – Microbiological methods – Part 2: Tests of

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EN ISO 11737-1 -2 - Microbiological control methods. Confirmed LR - LVS EN ISO 11737-1: 2006 /AC: 2009 Insight available at: https: //. lvs. lv/lv/std 4 /LVS%20 EN%20 ...

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... 2006 Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and embly processes (ISO 11607-2:2006) EN ISO 11737-1:2006 ...

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... Chest Seal is also biocompatible (cytotoxicity, irritation, and sensitization tested per ISO 10993), sterile (validated per ISO 11137-1:2006, ISO 11137-2:2007, ISO 11737 ...

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... EN 556:1994 + A1:1998 Note 2.1 Date expired (30.4.2002) CEN EN 556-1:2001/AC:2006 EN 556-2 ... 23.7.2008 EN 980:2003 Note 2.1 Date expired (31.5.2010) CEN EN ISO 11737-2:2009 ...