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Penumbra 5F Select Catheters

Device-Type

Guiding Catheters

Targated Speciality

Neuro vascular

Manufacturer

Penumbra

Penumbra Select Catheters are designed to enable primary delivery of our access devices for placement into final position and to eliminate the need for an over-the-wire exchange.


Features and Benefits

  • Engineered to aid selection off of arch into desired vessel
  • Designed to facilitate placement into distal vasculature
  • Large .040″ (1.02 mm) lumen
  • Compatible with .035″–.038″ (.89 mm–.97 mm) guidewires


  • 5 F (1.65 mm) Select designed for use with Neuron 070 and BENCHMARK 071


Safety informations

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.

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.


Neuron MAX System – Intended Use

The Neuron MAX System is intended for the introduction of interventional devices into the peripheral, coronary, and neuro vasculature.


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

Neuron Intracranial Access System

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 MAX System

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.


Benchmark Intracranial Access System

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.

Device Documents

Questions & Answers

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