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LaaGuarder™ Left Atrial Appendage Closure System

LaaGuarder™ by Shenqi Medical is a left atrial appendage closure system. Explore its device references, dedicated access and delivery components, and preparation for a product demonstration.

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  • Shenqi Medical · Structural Heart · LAA Closure

    LaaGuarder™ Left Atrial Appendage Closure System

    A catheter-delivered left atrial appendage closure system from Shanghai Shenqi Medical Technology Co., Ltd. The manufacturer describes its use in non-valvular atrial fibrillation patients at high stroke risk who are unsuitable for long-term anticoagulation.

    Official LaaGuarder illustration. Select the image to view the complete manufacturer graphic.

    Five device diameters

    The current manufacturer table lists 21, 24, 27, 30 and 33 mm devices, references LP0121, LP0124, LP0127, LP0130 and LP0133. These are catalogue options; anatomical assessment and the applicable IFU govern selection.

    Dedicated access and delivery

    The listed access sheath is 14F with a 770 mm effective length. The delivery catheter is 12F with an 830 mm effective length. The manufacturer highlights flexible petal tips in the device design.

    Start with a complete system discussion

    A useful evaluation connects the proposed implant to the whole service. Ask EUKON to identify the product reference, compatible dedicated components and documentation for the configuration being offered.

    • Which imaging and clinical assessment pathway will the team use?
    • Who will review device selection, implantation and follow-up?
    • Which access and delivery components are included in the proposed supply?
    • What operator training and supervised team education will be arranged?

    Bring clinical, technical and purchasing colleagues into the same discussion. Request the proposed configuration in writing so the department can check supply, consumables, traceability and support arrangements together.

    Make the demonstration practical

    Use a labelled model or manufacturer illustration to identify the closure device and distinguish the access sheath from the delivery catheter. Ask each participant to explain which component they would prepare, supply or document in their role.

    For a clinical introduction, request an authorised anonymised case discussion. Agree in advance which questions the session should answer, and record the points that require further manufacturer confirmation.

    Documentation and clinical use

    The manufacturer identifies CE certification M.2025.MDR.1061. Eligibility, preparation, release criteria, antithrombotic management and follow-up must follow the locally supplied IFU and the treating team’s assessment. A brochure or demonstration does not establish these requirements.

    Explore LaaGuarder with EUKON

    Contact us for a structural heart product discussion and a configuration review. Education supports technical familiarisation and team learning; arrange formal manufacturer training before clinical operation.

    Contact EUKON · Open Education

    Manufacturer source

    Reviewed 6 October 2026: Shenqi Medical LaaGuarder product information, including the English product introduction, design features and Models and Specifications panel. Confirm current local availability and supplied instructions with EUKON.

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