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Overview

The drug-coated balloon catheter Paclitaxel is intended for performing the procedure of percutaneous transluminal angioplasty (PTA) of peripheral arteries (iliac, femoral artery, arteries of the iliofemoral segment, popliteal artery, arteries of the leg, renal artery), as well as for eliminating obstructive lesions of natural or artificial arteriovenous fistulas.

Specifications

Diameter: 2, 2.5, 3.0, 3.5, 4.0, 5.0, 6.0, 7,0,8,0 mm
Length: 20, 40, 60, 80, 120, 150,200 mm
Catheter on delivery system (OTW)
Catheter working length:100 cm, 140 cm and 150 cm
Guide compatibility: 0.018’’(0.014’’ compatible)
Nip profile:0.019’’ maximum
Crossing profile:from 0.035’’ up to 0.063’’
Nominal pressure:7 atm
Rated burst pressure (RBP): 16 atm(8 mm diameter: 14 atm)
Average burst pressure (ABP): 20 atm

Clinical trials

Luminor has demonstrated its safety and effectiveness in long-term follow-up and across a variety of indications:

Multicenter, randomized and controlled trial, Luminor vs POBA.

82.10% fTLR
at 5 years

Prospective, multicenter trial, with Luminor and Angiolite BTK as bailout stenting in BTK.

81.6% fTLR
at 1 year

Prospective, single-arm, multicentre study to evaluate the efficacy and safety of BTK treatment

86.6% fTLR
at 1 year
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