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華盛昌(002980.SZ):公司是紅外人體測温領域的標杆企業,產品累計銷售超數百萬台
格隆匯 02-09 14:53

格隆匯2月9日丨華盛昌(002980.SZ)於2023年2月7日、2月8日接受機構調研時表示,公司是紅外人體測温領域的標杆企業,產品累計銷售超數百萬台,廣泛用於各級醫院、企事業單位、家庭和個人等場合,強大的研發實力,多年市場經營,公司積累大量的醫療客户資源和醫療器械產品研發、生產經驗。在醫療領域,公司看好家用醫療和體外診斷領域。

(1)家用醫療:家用醫療器械在歐美日發達國家己進入穩定成熟期,我國起步雖晚,但人口眾多,醫療衞生系統改善空間大,已是全球第二大醫療市場。近年來在亞健康羣體增加、慢病患者激增、老齡化加重等因素驅動下,家用檢測、康復治療類醫療器械需求逐步上升。公司以“將測量科技創新應用於醫療健康,使專業技術平價化,讓更多的人享受科技帶來的美好生活”為出發點,根據市場需求,研發相關產品。

(2)體外診斷:隨着人口老齡化、保險覆蓋率及支出不斷增加、收入增長等因素的驅動,加之體外診斷能夠便捷、低成本、低傷害的為醫護人員和個人提供精確、早期的臨牀診斷信息,為疾病發現、治療、監測提供有效依據,並能大大節省醫療費用,已成為醫療決策的重要依據。目前,體外診斷產業已成為當今世界上最活躍、發展最快的行業之一。公司自上市以來積極向醫療大健康領域拓展,憑藉以往積累的經驗和技術,在人體紅外測温技術平台的基礎上,深入IVD體外診斷醫療領域,建立了分子診斷技術平台、免疫層析技術平台,投資建立了新冠抗原檢測試劑研發實驗室和萬級潔淨生產車間,具有ISO13485醫療器械-質量管理體系認證、醫療器械生產許可和醫療器械經營許可資質。公司在疫情蔓延初期,投入建設免疫層析技術平台,加大新冠免疫層析膠體金抗原檢測產品研發投入,組建新冠抗原試劑研發團隊。公司新冠病毒抗原快速檢測試劑盒已取得歐盟專業類CE認證、自測類CE認證和俄羅斯註冊,在積極申報國內註冊。公司自研的實時熒光定量PCR分析儀已取得歐盟CE認證、英國MHRA註冊和美國FDA註冊,在積極申報國內註冊。公司建立了生物醫療實驗室,加強生物、醫學專業團隊建設,努力抓住醫療行業不斷呈現的新發展機遇。

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