GentleCath Air for Men; GentleCath Glide 间歇性导尿管; GentleCath Air for Women
K号: K252943 · 2026-04-01
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器械摘要
常见问题
What is the GentleCath Air for Men; GentleCath Glide Intermittent Catheter; GentleCath Air for Women?
GentleCath Air for Men; GentleCath Glide Intermittent Catheter; GentleCath Air for Women is a medical device that received FDA 510(k) clearance on 2026-04-01. The listed applicant is Convatec Limited. The 510(k) number is K252943.
When did GentleCath Air for Men; GentleCath Glide Intermittent Catheter; GentleCath Air for Women receive FDA 510(k) clearance?
GentleCath Air for Men; GentleCath Glide Intermittent Catheter; GentleCath Air for Women received FDA 510(k) clearance on 2026-04-01, under 510(k) number K252943.
Who is the listed applicant for GentleCath Air for Men; GentleCath Glide Intermittent Catheter; GentleCath Air for Women?
The FDA 510(k) record lists Convatec Limited as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GentleCath Air for Men; GentleCath Glide Intermittent Catheter; GentleCath Air for Women?
The FDA product code for GentleCath Air for Men; GentleCath Glide Intermittent Catheter; GentleCath Air for Women is EZD.
相关临床试验
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。
列明Convatec Limited为申报人的其他记录
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。
相关器械(代码:EZD)
关联记录通过名称、产品代码或其他元数据自动匹配。匹配不意味着已验证临床、科学、企业或监管关系;请查阅链接的官方来源。
官方来源
在 FDA 数据库中查看 →数据来源于FDA开放API。如需最新且权威的信息,请务必参考官方记录。
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