Luminor 14m

Paclitaxel-eluting balloon catheter

Safe and precise delivery of Paclitaxel

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iVascular advises that product IFUs should be downloaded, issued and reviewed for operators reference before or during procedures with our devices.


The Paclitaxel-eluting balloonLuminor 14m” is a coaxial catheter (OTW, over-the-wire) designed for percutaneous transluminal angioplasties of small peripheral arteries.

The guidewire runs into the inner lumen while the outer lumen is intended for contrast medium flow. The maximum diameter of the guide wire must not exceed 0.36 mm = 0.014 inches.

On the catheter’s distal part, just before the tip, there is the balloon (inflatable segment) that will dilate the artery upon inflating by means of infusion of contrast fluid inside it. The connector is Y-shaped and it has two entry ports:

  • The straight port is intended for guidewire passage.
  • The side port allows contrast medium flow to dilate the balloon.

The balloon is coated with a homogeneous mixture of Paclitaxel, a derivative of Taxol, and a  physiologically innocuous matrix, the excipient. The drug’s dose is 3 µg/mm2 of balloon surface and it is intended to avoid cellular proliferation, consequently decreasing re-intervention rate.

The drug is released from the balloon by means of a rapid inflation so that a high dose is released in a very short period of time. In order to assure a sufficient dosage of Paclitaxel onto the arterial wall, inflation process must last from 30 seconds to 1 minute. Dilation of the lesion can be optimized by using longer inflation times at operator’s discretion.

The balloon is designed to reach different diameters at different pressures, as predicted by the compliance curve included on the primary packaging.

Two radiopaque markers are located at each end of the balloon in order to mark its length and help the user to see the catheter while navigating inside the patient.

See IFU for further information. Available to download.


Dilatation of stenosis in femoral, popliteal and infra-popliteal arteries, with a nominal diameter from 1.5 mm to 4.0 mm and lengths from 40 mm up to 200 mm.


  • iVascular’s proprietary coating technology “Transfertech”. Nanotechnology drop dosage system that yields a multilayer thin coating.
  • Improved coating mechanical resistance. Better adhesion to the balloon
  • Homogeneous and precise Paclitaxel concentration of 3 µg/mm2 on the balloon for an effective treatment of the whole injury
  • Microcrystalline coating for faster drug absorption rate. Rapid release of Paclitaxel with long-term efficacy.
  • Segmented catheter design for excellent pushability and trackability. Balanced transition of forces. Anti-kinking performance.
  • 2 metallic radiopaque markers of Platinum / Iridium
  • Very short balloon deflation rates.
  • Wide balloon size range (200mm balloons)


  • Catheter materials: Nylon/Pebax (the product does not contain latex components)
  • Drug: 3 µg/mm2 Paclitaxel
  • Excipient: Organic ester. Lipophilic, biocompatible and biodegradable.
  • Balloon: Semi-compliant (10-15% from nominal pressure to RBP)
  • Nominal Presure: 7 atm
  • Rated Burst Pressure (RBP): 16 atm
  • Average Burst Pressure (AVP): 22 atm
  • Recommended guidewire: 0.014”
  • Crossing profile: from 0.026” up to 0.042”
  • Tip profile: 0.017”
  • Introducer compatibility: 4F for all diameters
  • Deflation time: < 5s
  • Available references
luminor 14m

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Clinical Support

Paclitaxel-eluting balloons have shown antiproliferative efficacy in the treatment and prevention of restenosis. Nevertheless, not all available devices are equally effective, which makes it interesting to compare results in a preclinical swine model (overexpansion 1.2 to 1.0). In this model, iVascular’s luminor 14m DEB significantly reduced in-stent restenosis compared with the control balloons. Study published in the Spanish Journal of Cardiology (Rev Esp Cardiol. 2014;67:456-62 – Vol. 67 Num.06) and available for download on website.

LUMINOR Registry: An observational, prospective and multicentre study with single-arm treatment for native stenotic or occlusive lesions or in-stent stenosis of the femoro-poplietal (FP) and below the knee (BTK) vessels. The objective is to evaluate the performance of luminor drug-eluting balloons in terms of primary patency and freedom of serious adverse events. A maximum of 250 Rutherford 2-5 cases will be recruited following an intention to treat basis.
Since Q3 2014 until Q2 2016, 215 cases with 252 lesions (121 CTO and 131 stenosis) have been included and monitored. Those were split as 154 FP and 86 BTK vessels treated. 12 cases combined both segments.
In the BTK subgroup the baseline demographics and lesion characteristics shown the ischemic status severity of patients. It is important to emphasize that 93% of patients were classified as Rutherford 4 or 5. Technical success was achieved in 97,4% of the cases. Bailout stenting was necessary in 3 lesions (2,6%).
30-day-mortality was 7,1%. At 1 year, primary patency was 88,3%, freedom from TLR 94,8%, freedom from major amputation 85,0% and survival 86,0%.

Package Contents

  • A paclitaxel-eluting dilatation balloon catheter OTW, covered by a protective shaft over the balloon and a protection stylet on the guidewire lumen. All the set is introduced in a circular dispenser to avoid damaging the catheter, and it is packed into a sterile bag.
  • One card with the compliance curve showing the nominal inflation pressure and the recommended maximum pressure
  • One leaflet with instructions for use


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iVascular advises that product IFUs should be downloaded, issued and reviewed for operators reference before or during procedures with our devices.