Tendril™ SDX Pacing Lead
CARDIOVASCULAR
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TendrilSDX

Pacing Lead

Tendril<sup>®</sup> SDX

PRODUCT HIGHLIGHTS

  • Radiopaque suture sleeve, ultra-thin lead body and Fast-Passcoating for easy implantation
  • Steroid elution and titanium nitride fractal coating on electrodes for low thresholds
  • Shorter tip-to-ring spacing and silicone insulation for high performance and reliability

ORDERING INFORMATION

Contents: Cardiac pacing lead


Reorder Number Insulation Fixation Minimum Introducer (F) Connector Length (cm)
1688TC/100 Silicone Rubber Ext/Ret Helix 7 IS-1 bipolar 100


Brief Summary: Prior to using these devices, please review the Instructions for Use for a complete listing of indications, contraindications, warnings, precautions, potential adverse events and directions for use. Devices depicted may not be available in all countries. Check with your St. Jude Medical representative for product availability in your country.

Indications: The Tendril SDX lead is designed for permanent sensing and pacing in either the atrium or the ventricle, in combination with a compatible pulse generator. An active lead, such as the Tendril SDX, may be indicated for patients where permanent fixation of passive leads is suspected to be unstable. In atrial applications, the use of a screw-in lead, such as the Tendril SDX, may be indicated in the presence of an abnormal, surgically altered or excised atrial appendage.

Contraindications: The Tendril SDX lead is contraindicated: In the presence of tricuspid atresia, for patients with mechanical tricuspid valves, in patients who are expected to be hypersensitive to a single dose of one milligram of dexamethasone sodium phosphate.

Adverse Events: Potential complications associated with the use of Tendril™ SDX leads are the same as with the use of other active fixation leads and include: cardiac tamponade, diaphragmatic stimulation, embolism, excessive bleeding, induced ventricular ectopy, infection, loss of pacing and/or sensing due to dislodgment or mechanical malfunction of the pacing lead, phrenic nerve stimulation, thrombosis. Complications reported with direct subclavian venipuncture include pneumothorax, hemothorax, laceration of the subclavian artery, arteriovenous fistula, neural damage, thoracic duct injury, cannulation of other vessels, massive hemorrhage and, rarely, death.

Refer to the User’s Manual for detailed indications, contraindications, warnings, precautions and potential adverse events.

Item GMCRM910EN

Last Updated: January 02, 2019

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