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Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO/DIS 10993-11:2025); German and English version prEN ISO 10993-11:2025

Biological evaluation of medical devices - Part 12: Sample preparation and reference materials - AMENDMENT 1 (ISO 10993-12:2021/FDAM 1:2025); German and English version EN ISO 10993-12:2021/FprA1:2025

Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices

Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics

Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables

Biological evaluation of medical devices - Part 17: Toxicological risk assessment of medical device constituents - Amendment 1 (ISO 10993-17:2023/DAM 1:2024); German and English version EN ISO 10993-17:2023/prA1:2024

Biological evaluation of medical devices - Part 23: Tests for irritation - Amendment 1: Additional in vitro reconstructed human epidermis models (ISO 10993-23:2021/DAM 1:2024); German and English version EN ISO 10993-23:2021/prA1:2024

Compressed air - Energy efficiency - Assessment

Ergonomic design of control centres - Part 3: Control room layout

Soil quality - Vocabulary (ISO 11074:2025); German version EN ISO 11074:2025

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