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Home » Prytime Gets CE Mark and UK Clearance for Next-Generation Catheter
Prytime Gets CE Mark and UK Clearance for Next-Generation Catheter
![CE mark](https://www.fdanews.com/ext/resources/images/ce-mark.gif?t=1627682539&width=430)
Prytime Medical Devices received both CE mark certification and UK approval for its ER-REBOA PLUS catheter.
The device has now been cleared in the UK and EU for controlling noncompressible truncal hemorrhages. It features a leave-behind guidewire capability up to 0.025 inches for use in endovascular procedures.
The Plus catheter previously received clearance from the FDA and Health Canada.
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