Biological evaluation of medical devices—Part 17:Establishment of allowable limits for leachable substances

Norma vydána dne 4.11.2005

Biological evaluation of medical devices—Part 17:Toxicological risk assessment of medical device constituents
K dispozici od: září 2026

Norma vydána dne 29.8.2025

Biological evaluation of medical devices—Part 18:Chemical characterization of medical device materials within a risk management process

Norma vydána dne 30.12.2022

Biological evaluation of medical devices—Part 19:Physico-chemical,morphological and topographical characterization of materials

Norma vydána dne 30.12.2022

Biological evaluation of medical devices - Part 2: Animal welfare requirements

Norma vydána dne 30.12.2011

Biological evaluation of medical devices—Part 2: Animal welfare requirements
K dispozici od: únor 2027

Norma vydána dne 28.1.2026

Biological evaluation of medical devices—Part 20:Principles and methods for immunotoxicology testing of medical devices

Norma vydána dne 10.12.2015

Biological evaluation of medical devices—Part 22:Guidance on nanomaterials

Norma vydána dne 30.12.2022

Biological evaluation of medical devices—Part 23:Tests for irritation

Norma vydána dne 27.11.2023

Biological evaluation of medical devices—Part 3:Tests for genotoxicity, carcinogenicity and reproductive toxicity

Norma vydána dne 4.6.2019