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CE Mark granted for ER-REBOA emergency occlusion balloon catheter in support of hemorrhage control.-Prytime Medical Devices.

Read time: 1 mins
Last updated:19th Nov 2016
Published:19th Nov 2016
Source: Pharmawand

Prytime Medical Devices, a company based outside of San Antonio, Texas formerly known as Pryor Medical Devices,has won CE Mark clearance to introduce its ER-REBOA emergency occlusion balloon catheter in Europe. Designed to occlude large vessels, the aorta in particular, it provides time for doctors to stabilize a patient before too much blood loss occurs.

In October 2015 the FDA granted 510(k) approval for the device to temporarily occlude large vessels using a balloon in support of hemorrhage control.

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