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Biological evaluation of medical devices - Part 17 : Establishment of allowable limits for leachable subtances

Publication details: Switzerland: International Organization of Standardization, 2002Edition: First edition

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Item type	Current library	Collection	Call number	Vol info	Status	Date due	Barcode
Standard	Perpustakaan LGM 260 Jalan Ampang	Reference	ISO 10993-17:2002 (Browse shelf(Opens below))	File SIRIM Standard 10000 - 13999	Available

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Previous	ISO 10993-1:1992 Biological evaluation of medical devices - Part 1: Guidance on selection of tests	ISO 10993-1:2018 Biological evaluation of nedical devices - Part 1 : Evaluation and testing within a risk management process	ISO 10993-12:2012 Biological evaluation of medical devices - Part 12: Sample preparation and reference materials	ISO 10993-17:2002 Biological evaluation of medical devices - Part 17 : Establishment of allowable limits for leachable subtances	ISO 10993-3:1992 Biological evaluation of medical devices - Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity	ISO 10993-4:1992 Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood	ISO 10993-5:1992 Biological evaluation of medical devices - Part 5: Test for cytotoxicity, in vitro methods	Next

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