Carotid stents

Protege RX

by Covidien LP

A non-bioabsorbable tubular device dedicated to implantation in a carotid artery to maintain arterial patency and improve luminal diameter in patients with atherosclerotic disease. It is made of metal [e.g., nickel-titanium alloy (Nitinol)] typically in a tubular mesh structure, and is typically delivered to the site of implantation by a dedicated instrument where it self-expands upon release. It is available in a variety of lengths and diameters and may be used in conjunction with an embolic protection device. Disposable devices associated with implantation may be included.

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Where to buy Protege RX

Contact Covidien LP directly; they can quote, ship, or point you to the distributor for your country.

From medtronic.com, checked October 2026.

No reply, or outside their markets? Send us a request and we route it to a rep or distributor for your country.

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Protege RX models and sizes

From the FDA Global Unique Device Identification Database. Confirm with the manufacturer's instructions for use.

Model / catalog no.SizeMRIStatus
SEBX-8-40-135Outer Diameter 8.00 mm; Length 135 cm; Catheter Gauge 6 Fr Not statedAvailable
SECX-6-20-135Length 20 mm; Catheter Gauge 6 Fr MR ConditionalAvailable
SECX-6-30-135Length 30 mm; Catheter Gauge 6 Fr MR ConditionalAvailable
SECX-6-40-135Length 40 mm; Catheter Gauge 6 Fr MR ConditionalAvailable
SECX-6-60-135Length 60 mm; Catheter Gauge 6 Fr MR ConditionalAvailable
SECX-7-20-135Length 20 mm; Catheter Gauge 6 Fr MR ConditionalAvailable
SECX-7-30-135Length 30 mm; Catheter Gauge 6 Fr MR ConditionalAvailable
SECX-7-40-135Length 40 mm; Catheter Gauge 6 Fr MR ConditionalAvailable
SECX-7-60-135Length 60 mm; Catheter Gauge 6 Fr; Outer Diameter 7 mm MR ConditionalAvailable
SECX-8-20-135Length 20 mm; Catheter Gauge 6 Fr MR ConditionalAvailable
SECX-8-30-135Length 30 mm; Catheter Gauge 6 Fr MR ConditionalAvailable
SECX-8-40-135Length 40 mm; Catheter Gauge 6 Fr MR ConditionalAvailable
SECX-8-60-135Length 60 mm; Catheter Gauge 6 Fr MR ConditionalAvailable
SECX-9-20-135Length 20 mm; Catheter Gauge 6 Fr MR ConditionalAvailable
SECX-9-30-135Length 30 mm; Catheter Gauge 6 Fr MR ConditionalAvailable
SECX-9-40-135Length 40 mm; Catheter Gauge 6 Fr MR ConditionalAvailable
SECX-9-60-135Length 60 mm; Catheter Gauge 6 Fr MR ConditionalAvailable
SECX-10-20-135Length 20 mm; Catheter Gauge 6 Fr MR ConditionalAvailable
SECX-10-30-135Length 30 mm; Catheter Gauge 6 Fr MR ConditionalAvailable
SECX-10-40-135Length 40 mm; Catheter Gauge 6 Fr MR ConditionalAvailable
SECX-10-60-135Length 60 mm; Catheter Gauge 6 Fr MR ConditionalAvailable

FDA clearances

  • PMA P060001 July 2024

Procedures that use carotid stents

Frequently asked questions

What is Protege RX used for?

A non-bioabsorbable tubular device dedicated to implantation in a carotid artery to maintain arterial patency and improve luminal diameter in patients with atherosclerotic disease. It is made of metal [e.g., nickel-titanium alloy (Nitinol)] typically in a tubular mesh structure, and is typically delivered to the site of implantation by a dedicated instrument where it self-expands upon release. It is available in a variety of lengths and diameters and may be used in conjunction with an embolic protection device. Disposable devices associated with implantation may be included.

Who makes Protege RX?

Protege RX is made by Covidien LP. It is listed under carotid stents, biliary drainage catheters in our device library.

What sizes does Protege RX come in?

Sizes listed for Protege RX: Length: 20–60 mm; Catheter Gauge: 6 Fr; Outer Diameter: 7 mm. Confirm availability with the manufacturer's instructions for use.

Is Protege RX MRI safe?

The FDA device database lists Protege RX as MR Conditional. Always follow the specific MRI conditions in the labeling.

Is Protege RX FDA cleared?

Protege RX is covered by FDA submission P060001.

How do I contact a Covidien LP sales representative?

Covidien LP has not listed representatives on LA Vascular yet. Visit the Covidien LP company page for contact details.

Models, sizes and MRI status come from the FDA Global Unique Device Identification Database (GUDID); descriptions marked "provided by the manufacturer" are reviewed before publishing. Not an endorsement; follow the manufacturer's instructions for use.

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