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Glavni meni

ISO 10993-18:2020

Biological evaluation of medical devices — Part 18: Chemical characterization of medical device materials within a risk management process
13. 1. 2020.

Опште информације

90.93     10. 6. 2025.

ISO

ISO/TC 194

Međunarodni standard

11.100.20  

engleski   francuski  

Kupovina

Objavljen

Jezik na kome želite da primite dokument.

Apstrakt

This document specifies a framework for the identification, and if necessary, quantification of constituents of a medical device, allowing the identification of biological hazards and the estimation and control of biological risks from material constituents, using a generally stepwise approach to the chemical characterization which can include one or more of the following:
— the identification of its materials of construction (medical device configuration);
— the characterization of the materials of construction via the identification and quantification of their chemical constituents (material composition);
— the characterization of the medical device for chemical substances that were introduced during manufacturing (e.g. mould release agents, process contaminants, sterilization residues);
— the estimation (using laboratory extraction conditions) of the potential of the medical device, or its materials of construction, to release chemical substances under clinical use conditions (extractables);
— the measurement of chemical substances released from a medical device under its clinical conditions of use (leachables).
This document can also be used for chemical characterization (e.g. the identification and/or quantification) of degradation products. Information on other aspects of degradation assessment are covered in ISO 10993-9, ISO 10993-13, ISO 10993-14 and ISO 10993-15.
The ISO 10993 series is applicable when the material or medical device has direct or indirect body contact (see ISO 10993-1 for categorization by nature of body contact).
This document is intended for suppliers of materials and manufacturers of medical devices, to support a biological evaluation.

Životni ciklus

PRETHODNO

POVUČEN
ISO 10993-18:2005

TRENUTNO

OBJAVLJEN
ISO 10993-18:2020
90.93 Odluka o potvrđivanju standarda
10. 6. 2025.

ISPRAVKE / IZMENE

OBJAVLJEN
ISO 10993-18:2020/Amd 1:2022

Nacionalna preuzimanja

Biološko vrednovanje medicinskih sredstava - Deo 18: Hemijska karakterizacija materijala medicinskih sredstava u okviru procesa upravljanja rizikom

60.60   Standard objavljen