AS ISO 10993.17-2004

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Specifies a method for the determination of allowable limits for substances leachable from medical devices. It describes a systematic process through which identified risks arising from toxicologically hazardous substances present in medical devices can be quantified. Not applicable to devices that have no patient contact, e.g. in vitro diagnostic devices. The Standard is identical to, and has been reproduced from, ISO 10993-17:2002.

Product Details

Edition:

1st

Published:

01/01/2004

ISBN(s):

0733762271

Number of Pages:

25

File Size:

1 file , 810 KB

Product Code(s):

10159165, 10159173, 10159143