Comparison of the Cobalt Content in Needles Stainless Steel.

Q3 Medicine
Laura Berardi
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引用次数: 0

Abstract

Cobalt (Co) alloys are used extensively in a wide range of medical devices due to their biocompatibility, durability, and properties. In 2017 the European Chemical Agency (ECHA) proposed to classify Co metal as a category 1B carcinogen (i.e. presumed to have carcinogenic potential for humans), as a reproductive hazard category 1B (i.e. presumed human reproductive toxicant) and as a category 2 mutagen. Even more, the European Medical Device Regulation (MDR) requires that medical devices contain > 0,1 w/w of substances that are category 1 A and 1B (CMR). As far as the European Medical Device Regulation, it is not specified if the Co content and concentration had to be determined/measured on the entire product or only on the product components. The object of this work is the comparison of Co profile in three different suppliers of stainless-steel needles as is and after being processed (i.e. sterilized) and then provide the proper interpretation and application of MDR requirements. The study and the extractable profile demonstrate the low cobalt content on needles and on a total syringe, thus suggesting to consider the Co content only on the syringe component.

针头不锈钢中钴含量的比较。
钴(Co)合金因其生物相容性、耐久性和特性,被广泛应用于各种医疗器械中。2017 年,欧洲化学品管理局(ECHA)提议将钴金属列为 1B 类致癌物(即推定对人类具有致癌潜力)、1B 类生殖危害物(即推定对人类具有生殖毒性)和 2 类致突变物。此外,《欧洲医疗器械法规》(MDR)还要求医疗器械必须含有大于 0.1 w/w 的第 1 A 类和第 1B 类(CMR)物质。就欧洲医疗器械法规而言,没有明确规定 Co 的含量和浓度是必须针对整个产品还是仅针对产品组件进行测定/测量。这项工作的目的是比较三家不同供应商的不锈钢针头在原样和加工(即灭菌)后的钴含量,然后对 MDR 要求进行适当的解释和应用。这项研究和可萃取曲线表明,针头和整个注射器中的钴含量都很低,因此建议只考虑注射器部件中的钴含量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
1.90
自引率
0.00%
发文量
34
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