由蛋鸡科(DSM 11798)菌株组成的用于猪和所有禽类(1m01)的饲料添加剂的更新授权评估(BIOMIN GmbH)

IF 3.3 3区 农林科学 Q2 FOOD SCIENCE & TECHNOLOGY
EFSA Panel on Additives and Products or Substances used in Animal Feed (FEEDAP), Roberto Edoardo Villa, Giovanna Azimonti, Eleftherios Bonos, Henrik Christensen, Mojca Durjava, Birgit Dusemund, Ronette Gehring, Boet Glandorf, Maryline Kouba, Marta López-Alonso, Francesca Marcon, Carlo Nebbia, Alena Pechová, Miguel Prieto-Maradona, Ilen Röhe, Katerina Theodoridou, Baltasar Mayo, Montserrat Anguita, Jaume Galobart, Jordi Ortuño, Fabiola Pizzo, Rosella Brozzi
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引用次数: 0

摘要

应欧盟委员会的请求,欧洲食品安全局被要求就含有 DSM 11798 细菌活细胞的制剂作为技术添加剂(功能类别:减少霉菌毒素对饲料污染的物质)用于猪和所有禽类饲料的授权续展申请提供科学意见。申请人提供的证据表明,目前市场上销售的添加剂符合现有的授权条款。活性剂的标识已经更改,它属于蛋壳菌科。欧洲食品安全局动物饲料中使用的添加剂和产品或物质专家小组(FEEDAP)得出结论认为,根据批准的授权条款,该添加剂对仔猪、育肥猪和所有禽类物种、消费者和环境仍然安全。在用户安全方面,该添加剂对皮肤和眼睛没有刺激性。然而,它应被视为皮肤和呼吸道致敏物质,任何通过皮肤和呼吸道的接触都是有风险的。这一结论原则上适用于任何含有该活性剂的制剂。在延长授权的情况下,没有必要评估该添加剂的功效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Assessment of the feed additive consisting of a strain belonging to Eggerthellaceae family (DSM 11798) for pigs and all avian species (1m01) for the renewal of its authorisation (BIOMIN GmbH)

Following a request from the European Commission, EFSA was asked to deliver a scientific opinion on the assessment of the application for renewal of the authorisation of the preparation containing viable cells of the bacterium DSM 11798 intended for use as a technological additive (functional group: substances for reduction of the contamination of feed by mycotoxins) in feed for pigs and all avian species. The applicant provided evidence that the additive currently on the market complies with the existing terms of the authorisation. The identification of the active agent has been changed and it belongs to the Eggerthellaceae family. The EFSA Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) concluded that the additive remains safe for piglets, pigs for fattening and all avian species, consumers and the environment under the approved terms of the authorisation. Regarding user safety, the additive is not a skin or eye irritant. However, it should be considered a skin and respiratory sensitiser, and any exposure through the skin and respiratory tract is a risk. This conclusion would apply, in principle, to any preparation containing the active agent. There is no need for assessing the efficacy of the additive in the context of the renewal of the authorisation.

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来源期刊
EFSA Journal
EFSA Journal Veterinary-Veterinary (miscellaneous)
CiteScore
5.20
自引率
21.20%
发文量
422
审稿时长
5 weeks
期刊介绍: The EFSA Journal covers methods of risk assessment, reports on data collected, and risk assessments in the individual areas of plant health, plant protection products and their residues, genetically modified organisms, additives and products or substances used in animal feed, animal health and welfare, biological hazards including BSE/TSE, contaminants in the food chain, food contact materials, enzymes, flavourings and processing aids, food additives and nutrient sources added to food, dietetic products, nutrition and allergies.
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