翻新 LigaSure XP Maryland 齿轮封口器/分隔器 无纳米涂层
K号: K260636 · 2026-06-18
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器械摘要
常见问题
What is the Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coating?
Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coating is a medical device that received FDA 510(k) clearance on 2026-06-18. The listed applicant is Stryker Sustainability Solutions. The 510(k) number is K260636.
When did Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coating receive FDA 510(k) clearance?
Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coating received FDA 510(k) clearance on 2026-06-18, under 510(k) number K260636.
Who is the listed applicant for Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coating?
The FDA 510(k) record lists Stryker Sustainability Solutions as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coating?
The FDA product code for Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coating is GEI.
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Stryker Sustainability Solutions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:GEI)
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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