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General| Technology | LigaSure Technology |
|---|---|
| Generator Compatibility | LigaSure generators |
| Application | Laparoscopic and open surgical procedures |
| Sterility | Sterile, single-use |
| Frequency | Generator dependent |
| Shaft Diameter | 5mm |
This reprocessed device is intended for single patient use, subject to physician order.
Defines symbols related to sterilization, reprocessing dates, and usage limitations.
Lists compatible generator models and software versions for the LF4318 instrument.
Details the instrument's dimensions, controls, and operation methods for sealing.
Specifies surgical procedures and vessel types for which the LF4318 is intended.
Lists conditions or scenarios where the device should not be used.
Highlights critical safety precautions and potential hazards associated with device use.
Covers initial checks, inspection, and connection procedures before surgery.
Details how to use the LigaSure system during surgery, including fire and pacemaker warnings.
Covers tissue manipulation, jaw rotation, vessel sealing, and tissue cutting procedures.
Details cautions regarding hot jaws, grasping tissue, electrical contact, and seal completion.
Explains how to clean jaws during use and addresses alert situations like incomplete seals.
Details the 'Check Instrument/Seal Cycle Incomplete' alert and corrective actions.
Provides guidance for incomplete seal cycles and reactivation procedures.
Covers instrument disposal, pre-clinical study findings, and transport/storage conditions.
Details Stryker's warranty for reprocessed products, excluding damages from original manufacturer.
Covers Stryker's warranty for products manufactured by Stryker itself.
Outlines express warranty, limitations of liability, and conditions for warranty claims.
