BS EN ISO 10993-3:2014
$189.07
Biological evaluation of medical devices – Tests for genotoxicity, carcinogenicity and reproductive toxicity
Published By | Publication Date | Number of Pages |
BSI | 2014 | 48 |
This part of ISO 10993 specifies strategies for risk estimation, selection of hazard identification tests and risk management, with respect to the possibility of the following potentially irreversible biological effects arising as a result of exposure to medical devices:
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genotoxicity;
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carcinogenicity;
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reproductive and developmental toxicity.
This part of ISO 10993 is applicable when the need to evaluate a medical device for potential genotoxicity, carcinogenicity, or reproductive toxicity has been established.
NOTE Guidance on selection of tests is provided in ISO 10993-1.
PDF Catalog
PDF Pages | PDF Title |
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4 | Foreword |
5 | Annex ZA (informative) Relationship between this European Standard and the Essential Requirements of EU Directive 93/42 EEC on medical devices Table ZA.1 — Correspondence between this European Standard and Directive 93/42/EEC on medical devices |
7 | Annex ZB (informative) Relationship between this European Standard and the Essential Requirements of EU Directive 90/385/EEC on active implantable medical devices Table ZB.1 — Correspondence between this European Standard and Directive 90/385/EEC on active implantable medical devices |
9 | Foreword |
11 | Introduction |
12 | Section sec_1 Section sec_2 1 Scope 2 Normative references |
13 | Section sec_3 Section sec_3.1 Section sec_3.2 Section sec_3.3 Section sec_3.4 Section sec_3.5 Section sec_3.6 Section sec_4 Section sec_4.1 3 Terms and definitions 4 Requirements for test strategies 4.1 General |
14 | Section sec_4.2 Section sec_4.3 4.2 Additional requirements for carcinogenicity testing 4.3 Additional requirements for reproductive toxicity testing |
15 | Section sec_5 Section sec_5.1 Section sec_5.2 Section sec_5.2.1 Section sec_5.2.2 5 Genotoxicity tests 5.1 General 5.2 Test strategy |
16 | Section sec_5.2.3 |
17 | Section sec_5.3 5.3 Sample preparation |
18 | Section sec_6 Section sec_6.1 Section sec_6.2 6 Carcinogenicity tests 6.1 General 6.2 Evaluation strategy |
19 | Section sec_6.3 Section sec_6.4 6.3 Sample preparation 6.4 Test methods |
20 | Section sec_7 Section sec_7.1 Section sec_7.2 7 Reproductive and developmental toxicity tests 7.1 General 7.2 Test strategy |
21 | Section sec_7.3 Section sec_7.4 7.3 Sample preparation 7.4 Test methods |
22 | Section sec_8 8 Test report |
23 | Annex sec_A Annex sec_A.1 Annex A (informative) Guidance on selecting an appropriate sample preparation procedure in genotoxicity testing |
24 | Annex sec_A.2 Annex sec_A.2.1 Annex sec_A.2.2 Annex sec_A.2.2.1 Annex sec_A.2.2.2 |
25 | Annex sec_A.2.2.3 Annex sec_A.2.3 Annex sec_A.3 Annex sec_A.3.1 |
26 | Figure fig_A.1 |
27 | Table tab_A.1 Annex sec_A.3.2 Annex sec_A.3.3 Annex sec_A.3.3.1 |
28 | Annex sec_A.3.3.2 Annex sec_A.3.3.3 |
29 | Annex sec_A.3.3.4 Annex sec_A.3.4 Annex sec_A.3.4.1 Annex sec_A.3.4.2 Annex sec_A.3.4.2.1 Annex sec_A.3.4.2.2 Annex sec_A.3.4.2.3 |
30 | Annex sec_A.3.4.2.4 Annex sec_A.3.4.2.5 Annex sec_A.4 Annex sec_A.4.1 Annex sec_A.4.2 Annex sec_A.4.3 |
31 | Annex sec_B Figure fig_B.1 Annex B (informative) Flowchart for follow-up evaluation |
32 | Annex sec_C Annex sec_C.1 Annex C (informative) Rationale of test systems |
33 | Annex sec_C.2 Annex sec_C.3 |
34 | Annex sec_D Annex D (informative) Cell transformation test systems |
35 | Annex sec_E Annex sec_E.1 Annex sec_E.2 Annex E (normative) Considerations for carcinogenicity studies performed as implantation studies |
36 | Annex sec_F Table tab_F.1 Annex F (informative) In vitro tests for embryo toxicity |
37 | Table tab_F.2 |
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