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ISO 10993-17:2002

Withdrawn

Withdrawn

A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.

Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substances

Available format(s)

Hardcopy , PDF 1 User , PDF 3 Users , PDF 5 Users , PDF 9 Users

Language(s)

English, French

Published date

27-11-2002

Withdrawn date

09-04-2025

$142.98
Including GST where applicable
Summarise this standard

ISO 10993-17:2002 specifies 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 hazardous substances present in medical devices can be quantified.

ISO 10993-17:2002 is not applicable to devices that have no patient contact (e.g. in vitro diagnostic devices).

Exposure to a particular chemical substance may arise from sources other than the device, such as food, water or air. ISO 10993-17:2002 does not address the potential for exposure from such sources.

DevelopmentNote
Supersedes ISO/DIS 10993-17. (12/2002)
DocumentType
Standard
Pages
25
PublisherName
International Organization for Standardization
Status
Withdrawn

⚠

This standard has been withdrawn and is no longer current. No replacement edition is available.

$142.98
Including GST where applicable