Biological evaluation of medical devices - Establishment of allowable limits for leachable substancesBS EN ISO 10993 17: 2009 Biological evaluation of medical devices. Establishment of allowable limits for leachable substances BS EN ISO 10993 17 specifies a method for the determination of allowable limits for substances leachable from medical devices. It is intended for use in deriving standards and estimating appropriate limits where standards do not exist. It describes a systematic process through which identified risks arising from toxicologically

Manufacturers and suppliers of shafts

whereas reducers have a larger male thread than female thread

BS 7371-12:2008 contains:

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and wear property of composite materials based on a high-purity alumina matrix with zirconia reinforcement for surgical implants

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or system administrators who are not end users

All dimensions given in this standard are nominal

and where appropriate the British Standard to which they should conform

NA to BS EN 1992-4 helps you in the design of fastenings for use in concrete

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NOTE 3 Where domestic cooking appliances are installed in commercial or industrial premises in conjunction with catering appliances