Risk Information
Caution:
Prior to use, please refer to the Instructions for Use for complete product indications, contraindications, warnings, precautions, potential adverse events, and detailed instructions for use.
BENCHMARK Intracranial Access System – Intended Use
The BENCHMARK Intracranial Access System is intended for the introduction of interventional devices into the peripheral, coronary, and neuro vasculature.
Potential Adverse Events
Possible complications include, but are not limited to, the following:
acute occlusion; air embolism; death; distal embolization; emboli; false aneurysm formation; hematoma or hemorrhage at puncture site; infection; intracranial hemorrhage; ischemia; neurological deficits including stroke; vessel spasm, thrombosis, dissection, or perforation.
NEURON Intracranial Access System – Intended Use
The NEURON Intracranial Access System is intended for the introduction of interventional devices into the peripheral, coronary, and neuro vasculature.
Potential Adverse Events
Possible complications include, but are not limited to, the following:
acute occlusion; air embolism; death; distal embolization; emboli; false aneurysm formation; hematoma or hemorrhage at puncture site; infection; intracranial hemorrhage; ischemia; neurological deficits including stroke; vessel spasm, thrombosis, dissection, or perforation.
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Overview
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.071″ (1.80 mm) lumen, enabling dual device delivery
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Proximal shaft engineered for support throughout aortic arch
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Full radiopaque distal shaft
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Offered pre-packaged with Penumbra 5 F (1.65 mm) Select™ Catheter, designed for coaxial delivery to final position without an over-the-wire exchange
Last Modified: October 2020
