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萬邦德(002082.SZ):子公司醫用外科口罩通過美國FDA 510 (K)審核
格隆匯 01-12 20:36

格隆匯1月12日丨萬邦德(002082.SZ)公佈,近日,公司控股子公司萬邦德醫療科技有限公司(“萬邦德醫療”)收到 U.S. Food and Drug Administration (美國食品藥品監督管理局,“美國FDA”)通知,萬邦德醫療醫用外科口罩正式通過美國FDA 510 (K)的審核

醫用外科口罩是一種一次性使用的平褶口罩,口罩內外層均為聚丙烯無紡布,中間層為由聚丙烯熔噴織物製成,鼻夾由聚丙烯和鐵絲製成,耳環由氨綸製成。此醫用外科口罩僅供一次性使用,以非無菌形式提供。

醫用外科口罩旨在防止患者和醫護人員之間微生物、體液和顆粒物質的轉移,減少血液和體液的潛在接觸。

公司本次醫用外科口罩產品通過美國 FDA 510 (K)的審核,標誌着公司生產醫用外科口罩獲得了美國市場的准入資格,有利於進一步增加公司產品開拓國際市場的綜合競爭力,帶動公司原有醫用防護口罩業務的發展,對公司未來的經營將產生積極影響。

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