Abstract
This document specifies the procedure for the assessment of medical devices and their constituent materials with regard to their potential to produce irritation. The tests are designed to predict and classify the irritation potential of medical devices, materials or their extracts according to ISO 10993‑1 and ISO 10993‑2.
This document includes:
— pre-test considerations for irritation, including in silico and in vitro methods for dermal exposure;
— details of in vitro and in vivo irritation test procedures;
— key factors for the interpretation of the results.
General information
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Status: PublishedPublication date: 2021-01
Corrected version (fr): 2021-02Stage: International Standard published [60.60] -
Edition: 1Number of pages: 60
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Technical Committee :ISO/TC 194ICS :11.100.20
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Life cycle
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Now
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Preliminary
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10
Proposal
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20
Preparatory
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30
Committee
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40
Enquiry
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50
Approval
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60
Publication
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90
Review
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95
Withdrawal
Amendments
Provide additional content; available for purchase; not included in the text of the existing standard.Under developmentISO 10993-23:2021/DAmd 1
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