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对由(原)帝斯曼12856组成的饲料添加剂进行评估,该添加剂适用于所有动物物种,以更新其授权(Lactosan GmbH & Co KG)。

Assessment of the feed additive consisting of (formerly ) DSM 12856 for all animal species for the renewal of its authorisation (Lactosan GmbH & Co KG).

作者信息

Bampidis Vasileios, Azimonti Giovanna, Bastos Maria de Lourdes, Christensen Henrik, Dusemund Birgit, Fašmon Durjava Mojca, Kouba Maryline, López-Alonso Marta, López Puente Secundino, Marcon Francesca, Mayo Baltasar, Pechová Alena, Petkova Mariana, Ramos Fernando, Sanz Yolanda, Villa Roberto Edoardo, Woutersen Ruud, Galobart Jaume, Vettori Maria Vittoria, Brozzi Rosella

出版信息

EFSA J. 2022 Feb 24;20(2):e07148. doi: 10.2903/j.efsa.2022.7148. eCollection 2022 Feb.

Abstract

Following a request from the European Commission, the Panel on Additives and Products or Substances used in Animal Feed (FEEDAP) was asked to deliver a scientific opinion on the assessment of the application for renewal of authorisation of (formerly ) DSM 12856 as a technological additive for use in forage for all animal species. The additive aims at improving the production of silage and is authorised for all animal species. The applicant has provided evidence that the additive currently on the market complies with the existing conditions of authorisation. There is no evidence to lead the FEEDAP Panel to reconsider its previous conclusions. Thus, the Panel concludes that the additive remains safe for all animal species, consumers and the environment under the authorised conditions of use. Regarding user safety DSM 12856 is not irritant to skin and eyes but is considered a skin and respiratory sensitiser. There was no need for assessing the efficacy of the additive in the context of the renewal of the authorisation.

摘要

应欧盟委员会要求,动物饲料添加剂及产品或物质专家委员会(FEEDAP)被要求就DSM 12856(原 )作为所有动物物种饲料用技术添加剂的授权续展申请评估发表科学意见。该添加剂旨在提高青贮饲料产量,已被授权用于所有动物物种。申请人已提供证据证明市场上现有的添加剂符合现有授权条件。没有证据促使FEEDAP专家委员会重新考虑其先前的结论。因此,专家委员会得出结论,在授权使用条件下,该添加剂对所有动物物种、消费者和环境仍然是安全的。关于用户安全,DSM 12856对皮肤和眼睛无刺激性,但被认为是皮肤和呼吸道致敏剂。在授权续展时无需评估该添加剂的功效。

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