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April 22, 2019

Surmodics' Sublime Guide Sheath Receives FDA Clearance

April 23, 2019—Surmodics, Inc. announced that it has received FDA 510(k) clearance for its Sublime guide sheath. The device is intended to introduce therapeutic or diagnostic devices into the vasculature, excluding the coronary and neuro vasculature, via radial artery access. The sheath will be available in 5- and 6-F diameters and 120- and 150-cm lengths.

According to the company, the highly flexible Sublime guide sheath is reinforced with Surmodics' Xtreme braid technology. It is designed to resist kinking and maximize strength while retaining a low profile. The Serene hydrophilic coating provides a lubricious surface along the entire working length of the guide sheath. It is preloaded with a dilator and has a hemostasis valve with side arm for flushing. The dilators are available with 0.018- and 0.035-inch guidewire compatibility.

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April 23, 2019

Rapid Medical Receives Financing to Support Development of Stroke Treatment Devices

April 23, 2019

Rapid Medical Receives Financing to Support Development of Stroke Treatment Devices