Comment Closes On
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|
Committee
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CH/150/2 |
Document Type
|
Draft |
ISBN
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|
Pages
|
|
Published
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|
Publisher
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British Standards Institution
|
Status
|
Withdrawn |
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 34:1979
|
Rubber, vulcanized — Determination of tear strength (trouser, angle and crescent test pieces) |
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 |
ASTM D 792 : 2013 : REDLINE
|
Standard Test Methods for Density and Specific Gravity (Relative Density) of Plastics by Displacement |
ASTM D 1044 : 2013 : REDLINE
|
Standard Test Method for Resistance of Transparent Plastics to Surface Abrasion |
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 11607:2003
|
Packaging for terminally sterilized medical devices |
ISO 11134:1994
|
Sterilization of health care products — Requirements for validation and routine control — Industrial moist heat sterilization |
ASTM D 1242 : 1995 : REV A
|
Standard Test Methods for Resistance of Plastic Materials to Abrasion (Withdrawn 2004) |
ISO 11137:1995
|
Sterilization of health care products Requirements for validation and routine control Radiation sterilization |
ISO 527-1:2012
|
Plastics Determination of tensile properties Part 1: General principles |
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