Comment Closes On
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Committee
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CH/150/2 |
Document Type
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Draft |
ISBN
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|
Pages
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|
Published
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|
Publisher
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British Standards Institution
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Status
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Withdrawn |
ISO 10993-4:2017
|
Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood |
ISO 11135:2014
|
Sterilization of health-care products Ethylene oxide Requirements for the development, validation and routine control of a sterilization process for medical devices |
ISO 8638:2010
|
Cardiovascular implants and extracorporeal systems Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters |
ISO 14937:2009
|
Sterilization of health care products General requirements for characterization of a sterilizing agent and the development, validation and routine control of a sterilization process for medical devices |
ISO 10993-11:2017
|
Biological evaluation of medical devices — Part 11: Tests for systemic toxicity |
ISO 10993-7:2008
|
Biological evaluation of medical devices Part 7: Ethylene oxide sterilization residuals |
ISO 10993-1:2009
|
Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
ISO 11134:1994
|
Sterilization of health care products — Requirements for validation and routine control — Industrial moist heat sterilization |
ISO 7000:2014
|
Graphical symbols for use on equipment Registered symbols |
ISO 11137:1995
|
Sterilization of health care products Requirements for validation and routine control Radiation sterilization |
ISO 594-2:1998
|
Conical fittings with 6 % (Luer) taper for syringes, needles and certain other medical equipment Part 2: Lock fittings |
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