Ruby^® Coil

Indication For Use
The Ruby Coil System is indicated for arterial and venous embolizations in the peripheral vasculature.
Contraindications
There are no known contraindications.
Warnings
• The RubyCoil System should only be used by physicians who have received appropriate training in interventional techniques.
Precautions
• The device is intended for single use only. Do not resterilize or reuse. Resterilization and/or reuse may compromise the structural integrity of the device or increase the risk of contamination or infection leading to device failure and/or cross-infection and potential patient injury, illness or death.
• Do not use kinked or damaged devices Do not use opened or damaged packages. Return all damaged devices and packaging to the manufacturer/distributor.
• Use prior to the “Use By” date.
• Use device in conjunction with fluoroscopic guidance.
• Do not advance or retract the device against resistance without careful assessment of the cause using fluoroscopy.
• Moving or torquing the device against resistance may result in damage to the vessel or device.
• Maintain a constant infusion of an appropriate flush solution
Potential Adverse Events
Potential complications include but are not limited to:
• acute occlusion
• air embolism
• death
• distal embolization
• emboli
• false aneurysm formation
• hematoma or hemorrhage at puncture/access site/site of entry
• infection
• intracranial hemorrhage
• ischemia
• neurological deficits including stroke
• vessel spasm, thrombosis, dissection or perforation
• thromboembolic episodes
• neurological deficits including stroke and possibly death
• vascular thrombosis
• post-embolization syndrome
• revascularization
• recanalization
• inadequate occlusion
• aneurysm rupture
• parent artery occlusion
• incomplete aneurysm filling

Indication For Use
The Penumbra Delivery Microcatheters are indicated to assist in the delivery of diagnostic agents, such as contrast media, and therapeutic devices, such as occlusion coils, to the peripheral and neuro vasculature.
Contraindications
There are no known contraindications.
Warnings
• The Penumbra Delivery Microcatheters should only be used by physicians who have received appropriate training in interventional techniques.
Precautions
• The devices are intended for single use only. Do not resterilize or reuse. Resterilization and/or Reuse may result in ineffective catheter coating lubrication, which may result in high friction and the inability to access the target location.
• Do not use kinked or damaged devices. Do not use open or damaged packages. Return all damaged devices and packaging to the manufacturer / distributor.
• Use prior to the “Use By” date.
• Use the Penumbra Delivery Microcatheters in conjunction with fluoroscopic visualization.
• Do not advance or withdraw the Penumbra Delivery Microcatheters against resistance without careful assessment of the cause using fluoroscopy. If the cause cannot be determined, withdraw the device. Moving or torquing the device against resistance may result in damage to the vessel or device.
• Maintain a constant infusion of appropriate flush solution.
• If flow through the device becomes restricted, do not attempt to clear the lumen by infusion. Remove and replace the device.
Potential Adverse Events
Possible complications include, but are not limited to, the following:
• Acute occlusion
• Hematoma or hemorrhage at access site
• Death
• Intracranial hemorrhage
• Hemorrhage
• Infection (at access site)
• Distal embolization
• Ischemia (cardiac and/or cerebral)
• Embolus (air, foreign body, thrombus, plaque)
• Aneurysm perforation
• False aneurysm formation
• Neurological deficits including stroke
• Vessel spasm, thrombosis, dissection, perforation or rupture
• Air embolism
• Emboli