At Teleflex, we provide a growing portfolio of innovation that can help you reduce costs, drive positive clinical outcomes, and increase patient satisfaction. We are committed to supporting our partnership with your facility through our Weck® 360 Service Program where we offer educational tools on Weck® applier care and maintenance.
All appliers should be cleaned and sterilized per instructions provided in the IFUs
Follow hospital, Association of the Advancement of Medical Instrumentation (AAMI), Association of Perioperative Registered Nurses (AORN), or regional standards for cleaning your appliers.
Opening the box lock:
Some Weck® Endoscopic Clip Appliers and Removers are provided with a cleaning port which permits access to the interior channels and cavities. Uncap the cleaning port, but do not remove the cap tether completely from the instrument. Flush with warm distilled or filtered water for approximately two minutes or until the visible gross debris is removed from the device.
Lubrication is essential every time instruments are processed. Do not use mineral oil, petroleum, or silicone-based products. Lubricate joints using a non-silicone, water-based surgical-grade lubricant.
Please examine endoscopic and open appliers and removers for potential damage before use in surgery. Pay particular attention to the jaws. Damaged or misaligned jaws may not allow clips to close acceptably for occlusion of intended structure. Damaged remover jaws may not allow for clip removal. If repair is required, clean, sterilize and return damaged instrument to Teleflex Medical.
Check the following components of your open clip appliers:
Your local Teleflex Surgical sales representative is your primary resource for support. Additional sales resources, including our sales trainers and regional management, are available for additional consultation as needed.
Caution: U.S. federal law restricts this device to sale by or on the order of a physician.
Weck Ligating Clips are contraindicated for use as a fallopian contraceptive tubal occlusion device and contraindicated for use in ligating the renal artery during laparoscopic donor nephrectomies.
Teleflex, the Teleflex logo, Hem-o-lok, Horizon, and Weck are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries. Other names may be trademarks of their respective owners.
Information in this material is not a substitute for the product Instructions for Use. Not all products may be available in all countries. Please contact your local representative.
© 2021 Teleflex Incorporated. All rights reserved. Revised 05/2021. MC-006240 Rev 2