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COPILOT Bleedback Control Valve
Indications & Important Safety Information ›› IFU (Full Version) ››
COPILOT Bleedback Control Valve - Because each drop lost is one too manyEngineered to Reduce Bleeding
The COPILOT Bleedback Control Valve / RHV is designed to reduce the blood loss commonly associated with interventional procedures.
The Difference Is in the Design
The COPILOT Valve's unique bleedback control seal features an innovative push-and-release mechanism. Opening the seal with a simple push facilitates the insertion and removal of devices. Once the seal is closed (released position), devices can still be moved freely.
Compatible With RX and OTW Platform Interventional Devices
Switching to the COPILOT Control Valve is simple and seamless. Abbott Vascular has designed the COPILOT valve to be completely compatible with a wide range of interventional devices on both rapid exchange and over-the-wire platforms.1
1 Less than or equal to 0.096" O.D. Data on file, Abbott Vascular.
Tests performed by and data on file at Abbott Vascular.
| Description | Contents | Part Number |
|---|---|---|
| COPILOT | COPILOT Bleedback Control Valve, single unit | 1003331 |
The COPILOT Bleedback Control Valve is also available in Priority Packs with other accessories. Please contact your sales representative or Abbott Customer Service for additional information.
AP2932925 Rev.A
Indications and Important Safety Information
COPILOT Bleedback Control Valve
INDICATIONS
The COPILOT Bleedback Control Valve is indicated for maintaining a seal around diagnostic/interventional devices with an outside diameter < .096" (2.44mm) during interventional procedures.
CONTRAINDICATIONS
The COPILOT Bleedback Control Valve is not intended for use with pressure injections > 400 psi.
WARNINGS
This device is intended for one time use only. Do NOT resterilize and/or reuse.
Do not inject any fluid if air bubbles are visible within the COPILOT Bleedback Control Valve.
To prevent damage to a balloon, it must be completely deflated during advancement/withdrawal through the COPILOT Bleedback Control Valve.
Failure to depress the cap prior to inserting a guide wire introducer could cause seal damage resulting in leakage and/or particulate embolization.
Failure to open the BBC seal and the clamp seal prior to inserting/withdrawing a diagnostic/interventional device could cause damage to the diagnostic/interventional device.
Power injection at pressures greater than 400 psi could result in leakage or detachment of components.
Care should be taken to avoid overtightening the clamp seal, as this may compromise the integrity of the diagnostic/interventional device lumen.
PRECAUTIONS
Prior to use, inspect the COPILOT Bleedback Control Valve for any damage. Do not use a damaged COPILOT Bleedback Control Device.


