The device is intended for use in the revascularization of acute ischemic stroke, within 8 hours of symptoms onset, caused by the intracranial occlusive vessels of patients who are not eligible for intravenous tissue plasminogen activator, IV tPA, or who fail IV tPA therapy.
The catheter is indicated for general intravascular use to facilitate introduction of diagnostic or therapeutic devices, including the neuro and peripheral vasculature.
This catheter is intended to temporarily or selectively block blood flow by expanding a balloon inside blood vessels during operations.
The micro catheter is intended for the controlled selective infusion of physician-specified therapeutic agents or contrast media into the vasculature of the peripheral and neuro anatomy.
The Aspiration System is intended for use in the revascularization of patients with acute ischemic stroke secondary to intracranial large vessel occlusive disease (within the internal carotid, middle cerebral M1 and M2 segments, basilar, and vertebral arteries) within 8 hours of symptom onset.
For medical institutions to use negative pressure to extract liquid and/or solids from the human body, including blood during and after surgery. It is not suitable for abortion and thoracic vacuum suction.
The device is intended for treatment of intracranial atherosclerosis. You can use it for dilatation of a stenosis in the cerebral arteries, meanwhile release the anti-proliferative drug to maintain the inner lumen and improve perfusion.
The device is indicated for use in improving cerebral artery lumen diameter in patients with intracranial atherosclerotic disease.
The device is indicated for dilatation of a stenosis in the cerebral arteries in order to improve perfusion.
The device is a neuro stent applied to patients suffer from TIA or stroke due to intracranial atherosclerosis.
The device is indicated for use as an embolic protection system to contain and remove embolic material (thrombus/debris) while performing angioplasty, stenting or thrombectomy procedures in coronary, peripheral and carotid arteries.
The occluder is a stroke prevention device designed to be permanently implanted at the opening of the LAA of patients with non-valvular atrial fibrillation (AF) to prevent thrombus escaping from the LAA, thus causing embolization.
The equipment houses the components and software needed to perform cryoablation procedures. It controls the delivery and disposal of cryoablation refrigerant safely and efficiently.
The device is intra-cardiac electrophysiology diagnostic catheter, which allow for the assessment of pulmonary vein isolation during the cryoablation procedure. The catheter is deployed through the cryoballoon guide wire lumen, minimizing the number of catheter exchanges and allowing the procedure to be performed using a single transseptal puncture. The catheter may also provide recording of real-time PV potentials during cryoablation with the cryoballoon.
The device delivers a refrigerant through an inflatable balloon to freeze tissue and disable unwanted electrical signals that contribute to AF originated from pulmonary vein.
The sheath is a unidirectional, deflectable sheath used to help position an ablation catheter and facilitates better positioning and maneuverability in coronary artery and chamber and peripheral artery
The system is intended for the endovascular embolization of intracranial aneurysms and other neurovascular abnormalities such as arteriovenous malformations and arteriovenous fistulae. It is also intended for vascular occlusion of blood vessels within the neurovascular system to permanently obstruct blood flow to an aneurysm or other vascular malformation and for arterial and venous embolization in the peripheral vasculature.
The device is indicated for the endovascular treatment of adults (22 years of age or older) with large or giant wide-necked intracranial aneurysms (IAs) in the internal carotid artery from the petrous to the superior hypophyseal segments.
The device is intended for use with embolic coils for the treatment of intracranial neurovascular diseases
The device is indicated for femoral artery puncture site closure, reducing times to hemostasis and ambulation in patients who have undergone diagnostic or interventional catheterization procedures using a standard 5F, 6F, or 7F vascular sheath introducer with up to a 12cm working length.
The guide wire is indicated for general intravascular use to aid in the selective placement of catheters in the peripheral and cerebral vasculature during diagnostic and/or therapeutic procedures.
The device can be applied to cerebral and coronary blood vessels and peripheral blood vessels to help deliver diagnostic or therapeutic catheters and devices into the vessel.
The catheter is intended for the introduction of non-liquid interventional devices (such as coils/stents/flow diverters) and infusion of diagnostic (such as contrast media) or non-liquid therapeutic agents into the neuro, peripheral, and coronary vasculature.