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Arterial Clamp

For the safety of centrifugal perfusion

Arterial Clamp Image
Arterial Clamp

The arterial clamp is designed for operation with the centrifugal pump for the safety of centrifugal perfusion.

 

When certain conditions are detected (low level, bubble or retrograde flow), an alarm is triggered, and the arterial clamp occludes the arterial line immediately to minimize the danger of air delivery.

Arterial Clamp
Safety Information

1. INDICATIONS FOR USE / INTENDED PURPOSE

EU: The Stöckert S5 System /Sorin Centrifugal Pump System (CP5) /Electrical Venous Occluder (EVO) /Electrical Remote-Controlled Tubing Clamp are intended to perform, control, monitor and support extracorporeal blood circulation replacing the mechanical pumping function of the heart, monitoring and regulating physiologic parameters during procedures requiring extracorporeal circulation.

US: The Stöckert S5 System is intended to be used during cardiopulmonary bypass for procedures lasting six (6) hours or less. Canada: In accordance with the applicable regulations, the Stöckert S5 System is used to perform, control and monitor extracorporeal blood circulation during an operation.

2. CONTRAINDICATIONS

There are no known contraindications for the Stöckert S5 System.

3. WARNINGS

The device must be used in accordance with the instructions for use. For a complete listing of warnings, please refer to the Instructions for Use which accompany each product

4. PRECAUTIONS

Federal law (U.S.A.) restricts this device to sale by or on the order of a physician. For a complete listing of precautions/cautions please refer to the Instructions for Use which accompany each product

The devices should be used by qualified and skilled personnel, able to follow the indications and instructions for use contained in the information provided by the manufacturer. Please contact us through our website (www.sorinmanuals.com) to receive instructions for use containing full prescribing information including indications, contraindications, warnings, precautions and adverse events.

The information contained in this summary represents partial excerpts taken from the product labeling. The information is not intended to serve as a substitute for a complete and thorough understanding of the device nor does this information represent full disclosure of all pertinent information concerning the use of this product.

Legal Manufacturer:

LivaNova Deutschland

Lindberghstrasse 25

D-80939 Munich, Germany

Distributed in the USA by:

LivaNova USA

14401 W 65th Way

Arvada, CO 80004

 

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