ISO 10993-23:2021 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.
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Edition: 1st Published: 01/01/2021 Number of Pages: 68 File Size: 1 file , 2.6 MB Same As: BS EN ISO 10993-23:2021, DIN EN ISO 10993-23 Note: This product is unavailable in Ukraine, Russia, Belarus