ENHANCE STABILITY FROM THE START

A THREE-DIMENSIONAL APPROACH TO ANEURYSMS

Provides an even distribution of coil loops at the treatment site

• Designed to provide greater coverage1
• Conforms to diverse morphologies1
• Available in .018” and 035” systems

The Azur system is intended to reduce or block the rate of blood flow in vessels of the peripheral vasculature. It is intended for use in the interventional radiologic management of arteriovenous malformations, arteriovenous fistulae, aneurysms, and other lesions of the peripheral vasculature. This device should only be used by physicians who have undergone training in the use of the Azur system for embolization procedures as prescribed by a representative from Terumo or a Terumo-authorized distributor. 

CONTRAINDICATIONS

Use of the Azur system is contraindicated in any of the following circumstances:

• When superselective coil placement is not possible.

• When end arteries lead directly to nerves.

• When arteries supplying the lesion to be treated are not large enough to accept emboli.

• When the A-V shunt is larger than the coil.

• In the presence of severe atheromatous disease.

• In the presence of vasospasm (or likely onset of vasospasm). 

Potential complications include, but are not limited to: hematoma at the site of entry, vessel/aneurysm perforation, unintended parent artery occlusion, incomplete filling, vascular thrombosis, hemorrhage, ischemia, vasospasm, edema, coil migration or misplacement, premature or difficult coil detachment, clot formation. revascularization, post-embolization syndrome, and neurological deficits including stroke and possibly death. The physician should be aware of these complications and instruct patients when indicated. Appropriate patient management should be considered.