维力医疗(603309.SH)发布公告，公司于近日收到广东省药品监督管理局颁发的《中华人民共和国医疗器械注册证》，涉及产品：“一次性使用可视双腔支气管插管”。

本次注册的“一次性使用可视双腔支气管插管”是原有产品可视双腔支气管插管的升级产品，升级后的产品可通过无线WiFi直接连接显示屏，不再需要连接线，临床使用更便捷、更安全。根据国家药品监督管理局官网数据查询了解到的信息，截至目前，国内暂无同行业厂家取得同类产品注册证。

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