FDA 510(k)

再製LigaSure XP Maryland 齒輪式封合器/分隔器，無納米塗層

K 號：K260636 · 2026-06-18

決定日期2026-06-18

產品代碼GEI

諮詢委員會SU 請提供完整的描述文本，以便我進行翻譯。

決定相當於

器材摘要

Remanufactured LigaSure XP Maryland Jaw Sealer/Divider Without Nano-coating is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Sustainability Solutions. It received FDA 510(k) clearance on 2026-06-18 under 510(k) number K260636. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

常見問題

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.

其他以 Stryker Sustainability Solutions 為申請人之記錄

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相關器械（代碼：GEI）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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官方來源

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