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CAPSUREFIX NOVUS MRI™ SURESCAN®

5076 MRI Lead Specifications

MR-Conditional
Initial Implant
MR
Existing Implant

Physical Characteristics
Polarity Bipolar
Shape Straight
Chamber Atrium/Ventricle
Fixation Helical Screw-
Extendable/Retractable
MR-Conditional 35, 45, 52, 58, 65, 85 cm Electrode Surface Area
Lengths Helix 4.2 mm2
Contraindicated 110 cm Ring 22 mm 2
for MRI*
Connector IS-1 BI Other Characteristics
DXAC
Materials Steroid (Dexamethasone Acetate)
Inner/Outer Insulation Silicone (MED-4719) 1.0 mg maximum
Conductor MP35N Helix Length 1.8 mm
Distal Electrode Platinized Helix Tip-to-Ring Spacing 10 mm
Ring Electrode Conductor Resistance 58 cm
Connector pin: Platinized
Connector ring: Stainless Steel Unipolar 33 Ω
Bipolar 61 Ω
Diameter Serial Prefix PJN
Body 2.0 mm (6 Fr)
Helix O.D. 1.17 mm Stylets
Ring Electrode 2.0 mm Inserted Gray Straight
Packaged (1) Blue J
Recommended introducer Size (1) Gray J
Without Guide Wire 7 Fr (1) Blue Straight
(1) Gray Straight
With Guide Wire 9 Fr
(1) White J

* Lead length is contraindicated because it was not tested in the MR environment.


Brief Statement: SureScan® Pacing Systems

Medtronic SureScan pacing systems are MR Conditional and as such are Contraindications
designed to allow patients to undergo MRI under the specified conditions Medtronic SureScan pacing systems are contraindicated for:
for use. A complete SureScan pacing system, which consists of an MRI • Concomitant implantation with another bradycardia device
SureScan device with two SureScan leads, is required for use in the MRI • Concomitant implantation with an implantable cardioverter defibrillator
environment. Consult the device manuals to ensure all system components
There are no known contraindications for the use of pacing as a
are MR Conditional.
therapeutic modality to control heart rate. The patient’s age and medical
Indications condition, however, may dictate the particular pacing system, mode of
Medtronic SureScan pacing systems are indicated for the following: operation, and implant procedure used by the physician.
• Rate adaptive pacing in patients who may benefit from increased pacing • Rate-responsive modes may be contraindicated in those patients who
rates concurrent with increases in activity cannot tolerate pacing rates above the programmed Lower Rate
• Accepted patient conditions warranting chronic cardiac pacing include: • Dual chamber sequential pacing is contraindicated in patients with
– Symptomatic paroxysmal or permanent second or third-degree chronic or persistent supraventricular tachycardias, including atrial
AV block fibrillation or flutter
– Symptomatic bilateral bundle branch block • Asynchronous pacing is contraindicated in the presence (or likelihood) of
– Symptomatic paroxysmal or transient sinus node dysfunctions with competition between paced and intrinsic rhythms
or without associated AV conduction disorders • Single chamber atrial pacing is contraindicated in patients with an AV
– Bradycardia-tachycardia syndrome to prevent symptomatic bradycardia conduction disturbance
or some forms of symptomatic tachyarrhythmias • ATP therapy is contraindicated in patients with an accessory antegrade
Note: The Advisa MRI™ pacing system includes the following additional pathway
indication:
Warnings and Precautions
– Vasovagal syndromes or hypersensitive carotid sinus syndromes
Changes in patient’s disease and/or medications may alter the efficacy of
The systems are also indicated for dual chamber and atrial tracking modes the device’s programmed parameters. Patients should avoid sources of
in patients who may benefit from maintenance of AV synchrony. Dual magnetic and electromagnetic radiation to avoid possible underdetection,
chamber modes are specifically indicated for treatment of conduction inappropriate sensing and/or therapy delivery, tissue damage, induction
disorders that require restoration of both rate and AV synchrony, which of an arrhythmia, device electrical reset, or device damage. Do not place
include: transthoracic defibrillation paddles directly over the device. Use of the
• Various degrees of AV block to maintain the atrial contribution to cardiac device should not change the application of established anticoagulation
output protocols.
• V VI intolerance (for example, pacemaker syndrome) in the presence of Patients and their implanted systems must be screened to meet the MRI
persistent sinus rhythm Conditions of Use. Do not scan patients who do not have a complete
Medtronic SureScan pacing system consisting of a SureScan device and
Antitachycardia pacing (ATP) is indicated for termination of atrial
two SureScan leads; patients who have broken, abandoned or intermittent
tachyarrhythmias in bradycardia patients with one or more of the above
leads; or patients who have a lead impedance value of
pacing indications.
< 200 Ω or > 1,500 Ω. Do not scan patients with a SureScan pacing system
implanted in sites other than the left or right pectoral region.
Potential Complications
Potential complications include, but are not limited to, rejection
phenomena, erosion through the skin, muscle or nerve stimulation,
oversensing, failure to detect and/or terminate arrhythmia episodes,
acceleration of tachycardia, and surgical complications such as hematoma,
infection, inflammation, and thrombosis. Potential lead complications
include, but are not limited to, valve damage, fibrillation, thrombosis,

UC201305283 EN © Medtronic, Inc. 2014. Minneapolis, MN. All Rights Reserved. Printed in USA. 09/2014
thrombotic and air embolism, cardiac perforation, heart wall rupture,
cardiac tamponade, pericardial rub, infection, myocardial irritability, and
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pneumothorax. Other potential complications related to the lead may
include lead dislodgement, lead conductor fracture, insulation failure,
World Headquarters threshold elevation, or exit block. The SureScan system has been designed
Medtronic, Inc. to minimize potential complications in the MRI environment. Potential
710 Medtronic Parkway MRI complications include, but are not limited to, lead electrode heating
Minneapolis, MN 55432-5604
USA and tissue damage resulting in loss of sensing or capture or both, or
Tel: (763) 514-4000 induced currents on leads resulting in continuous capture, VT/VF, and/or
Fax: (763) 514-4879 hemodynamic collapse.
Medtronic USA, Inc. See the device manuals before performing an MRI Scan for detailed information
Toll-free: 1 (800) 328-2518 regarding the implant procedure, indications, MRI conditions of use,
(24-hour technical support for
physicians and medical professionals) contraindications, warnings, precautions, and potential complications/adverse
events. For further information, call Medtronic at 1 (800) 328-2518 and/or consult
Medtronic’s website at www.medtronic.com.
Caution: Federal law (USA) restricts these devices to sale by or on the
order of a physician.