Amplatzer Delivery System

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Amplatzer™ Duct Occluders Abbott

    https://www.structuralheartsolutions.com/us/index.php?id=131&L=0
    The AMPLATZER TM Duct Occluder and 180° Delivery System should only be used by those physicians trained in transcatheter defect closure techniques. Physicians must be prepared to deal with urgent situations which require removal of embolized devices that result in critical hemodynamic compromise. This includes the availability of an on-site surgeon.

TM Septal Occluder and Delivery System

    https://professional.sjm.com/~/media/pro/resources/ifu/amplatzer-us/sh-asd/600208-011_ASD_eIFU_Secure_amplatzer_septal_occluder_us.ashx
    The AMPLATZER Delivery System is intended to facilitate the attachment, loading, delivery, and deployment of the AMPLATZER Septal Occluder device. See Figure 2 for the delivery system …

Duct Occluder and Delivery System - SJM

    https://professional.sjm.com/~/media/pro/resources/ifu/amplatzer-us/sh-pda/600207-008_PDA_eIFU_clean_amplatzer_duct_occluder_us.ashx
    The AMPLATZER 180° Delivery System is composed of a delivery sheath, dilator, loader, plastic vise, and delivery cable. 180° indicates the curve of the delivery sheath. Indications and Usage The AMPLATZER Duct Occluder is a percutaneous, transcatheter occlusion device intended for the nonsurgical closure of a patent ductus arteriosus (PDA).

TorqVue™ 45° and 180° Delivery Systems

    https://manuals.sjm.com/~/media/manuals/product-manual-pdfs/f/c/fcba81dd-ae2f-46fb-9306-40d1418d6240.pdf
    The AMPLATZER™ TorqVue™ delivery system is intended to provide a pathway through which devices are introduced within the chambers and coronary vasculature of the …

Class 2 Device Recall AMPLATZER Delivery System

    https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRES/res.cfm?id=71805
    The AMPLATZER Delivery System was designed to facilitate attachment, loading, delivery and deployment of the AMPLATZER Septal Occluder and comprised of a delivery …

Duct Occluder and Delivery System

    https://manuals.sjm.com/~/media/manuals/product-manual-pdfs/1/6/166a8499-7df8-4502-82b8-1ab2d0bd6cc7.pdf
    The AMPLATZER™ 180° Delivery System is composed of a delivery sheath, dilator, loader, plastic vise, and delivery cable. 180° indicates the curve of the delivery sheath. Indications and Usage The AMPLATZER™ Duct Occluder is a percutaneous, transcatheter occlusion device intended for the nonsurgical closure of a patent ductus arteriosus (PDA).

Amplatzer™ Septal Occluder Features Abbott

    https://www.structuralheartsolutions.com/us/index.php?id=120&L=0
    amplatzer tm septal occluder and delivery system INDICATION FOR USE The AMPLATZER TM Septal Occluder is a percutaneous, transcatheter, atrial septal defect closure device intended for the occlusion of atrial septal defects (ASD) in secundum position or patients who have undergone a fenestrated Fontan procedure and who now require closure of the fenestration.

For Patients - Amplatzer Portfolio

    https://www.myamplatzer.com/patients/
    The AMPLATZER™ Muscular VSD Occluder and delivery system should only be used by those physicians trained in transcatheter defect closure techniques. Physicians must be prepared to deal with urgent situations, such as device embolization, which require removal of the device. This includes the availability of an on-site surgeon.

Amplatzer PFO Occluder Centennial Heart Cardiovascular ...

    https://centennialheart.com/patient-center/patient-education/amplatzer.dot
    The AMPLATZER PFO Occluder is a percutaneous, transcatheter occlusion device intended to close all types of PFO's (i.e., classical as well as those with aneurysm of the septum) in patients with a history of stroke or transient ischemic attacks (TIA's)). U.S.A. Humanitarian Use DeviceLocation: 2400 Patterson St Suite 502, Nashville, 37203, TN

Amplatzer PFO Occluder PFO Closure Device

    https://www.cardiovascular.abbott/us/en/hcp/products/structural-heart/amplatzer-pfo.html
    The AMPLATZER™ PFO Occluder device consists of a nickel-titanium alloy, which is generally considered safe. However, in vitro testing has demonstrated that nickel is released from this device for a minimum of 60 days.

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