欧盟评估布氏乳杆菌DSM 22501作为所有动物饲料添加剂的授权更新申诶�/h1>

时间�?024-01-22 10:51 来源：食品伙伴网 作者： 泽夕

核心提示�?024�?�?9日，欧盟食品安全局（EFSA）发布消息，欧盟食品安全局发布关于布氏乳杆菌DSM 22501作为所有动物饲料添加剂的授权更新申请的评估、�/div>

　　 食品伙伴网讯2024�?�?9日， 欧盟食品安全局＇�a href='//www.sqrdapp.com/news/tag_10.html' class='zdbq' title='EFSA相关食品资讯' target='_blank'>EFSA）发布消息，欧盟食品安全局发布关于布氏 乳杆菋�/a>DSM 22501作为所月�a href='//www.sqrdapp.com/news/tag_4566.html' class='zdbq' title='动物相关食品资讯' target='_blank'>动物 饲料添加剁�/a>的授权更新申请的评估�

　　经过评估，专家小组得出结论，该添加剂在授权使用条件下对所有动物物种、消费者和环境都是安全的。在授权更新的情况下，无需评估添加剂的功效。部分原文报道如下：

　　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 additive co nsisting of Lentilactobacillus buchneri DSM 22501 as a technological feed additive to improve ensiling of fresh material for all animal species. The applicant has provided evidence that the additive currently on the market complies with the existing co nditions of authorisation. There is no new evidence that would lead the FEEDAP Panel to reco nsider its previous conclusions. Thus, the Panel co ncludes that the additive remains safe for all animal species, co nsumer and the enviro nment under the authorised co nditions of use. Regarding user safety, the additive is not irritant to skin and eye, but owing to its proteinaceous nature it should be co nsidered a respiratory sensitiser. No co nclusions could be drawn on the skin sensitisation potential of the additive. There is no need for assessing the efficacy of the additive in the co ntext of the renewal of the authorisation.

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日期９�a href="//www.sqrdapp.com/news/2024-01-22.html">2024-01-22

地区９�/font>欧盟国外
行业９�/font>添加剂配斘�/font>乳业进出叢�/font>
标签９�/font>动物乳杆菋�/font>饲料添加剁�/font>欧盟食品安全局EFSA
科普９�/font>动物乳杆菋�/font>饲料添加剁�/font>欧盟食品安全局EFSA

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