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U6ULTRA35SHA

DxTerity™ TRA diagnostic catheter

The DxTerity™ TRA cardiac and vascular diagnostic catheters are indicated to deliver radiopaque media, guidewires and therapeutic agents to selected sites.

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Indications, Safety, and WarningsIndicationsDxTerity™ diagnostic catheters are indicated for cardiac and vascular procedures. The diagnotic catheters are designed to deliver radiopaque media, guidewires, and theraputic agents to selected sites in the cardiovascular system. The different configurations of the diagnostic catheter are designed to be used in arteries, from access sites such as the radial, brachial, and femoral arteries.ContraindicationsNone specific to this device.General warnings and precautions

Read all instructions carefully. Failure to follow the instructions, warnings, and precautions may lead to serious consequences or injury to the patient.

Warning: This device was designed for single-patient use only. Do not reuse, reprocess, or resterilize this product. Reuse, reprocessing, or resterilization may compromise the structural integrity of the device or create a risk of contamination of the device, which could result in patient injury, illness, or death.

Visually inspect all sterile-barrier packaging before use. If the device is damaged or the integrity of the sterilization barrier has been compromised, do not use the product. Contact your Medtronic representative for return information.

Do not use after the Use-by date.

Use aseptic technique during the entire procedure.

Warning: Administer appropriate anticoagulation therapy to reduce potential thrombosis. If the patient is not appropriately anticoagulated, thrombus formation may occur. Testing without anticoagulation shows variable amounts of thrombus formation on the device surface.

After use, this product may be a biohazard. Handle and dispose of all such devices in accordance with accepted medical practice and applicable local, state, and federal laws and regulations.

Only physicians trained in intravascular angiographic procedures should use or supervise use of the diagnostic catheter.

Select a diagnostic catheter with an optimal tip shape and optimal size, taking into account the access site, the target site, and the patient’s anatomy. Carefully inspect the diagnostic catheter before use to verify that the size, shape, and condition of the catheter are suitable for the intended procedures.

Store the device at room temperature in a dry place. Keep away from sunlight or UV light.

The diagnostic catheter is supplied sterile and nonpyrogenic.

Do not heat or bend the diagnostic catheter before use.

Adverse eventsAdverse events that may occur or require intervention include, but are not limited to, the following conditions:

Thrombus formation

Embolization

Infection

Arterial, venous, or heart wall damage or perforation

Hematoma at puncture site

Cardiac arrhythmia

Myocardial infarction

Vascular occlusion

Death

Access pain site

Allergic and neurological reactions

Stroke and transient ischemic attack

Vasospasm

False aneurysm

Arteriovenous fistula

If a serious incident related to the device occurs, immediately report the incident to Medtronic and the applicable competent authority or regulatory body.Caution: Federal (USA) law restricts this device to sale by or on the order of a physician. See package inserts for the full product information.UC202311547 EN

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U6ULTRA35SHA

DxTerity™ TRA diagnostic catheter

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U6ULTRA35SHA DxTerity™ TRA diagnostic catheter

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United States

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U6ULTRA35SHA

DxTerity™ TRA diagnostic catheter