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Effortless Deliverability. Exceptional Outcomes.

Ranger Drug-Coated Balloon

Ranger™️drug-coated balloon consistently delivers exceptional outcomes with effortless deliverability

Ranger™ consistently delivers exceptional outcomes with effortless deliverability

Restenosis poses a significant, prevalent challenge in superior femoral artery (SFA) management. Boston Scientific is dedicated to overcoming peripheral arterial disease (PAD) challenges with bold innovation using next-generation drug-eluting technology. Boston Scientific is the first company to voluntarily evaluate our drug-coated balloon against another drug-coated balloon (DCB) in a level-1 randomised controlled trial for comparative effectiveness.

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Consistently high 12-month primary patency demonstrated across multiple randomised controlled trials (RCT)1,2

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Similar outcomes observed with low dose Ranger Drug-Coated Balloon (DCB) compared to higher dose IN.PACT2 DCB

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Significantly lower 12-month clinically driven target lesion revascularisation (CD-TLR) rate with Ranger versus uncoated percutaneous transluminal angioplasty (PTA)1

RANGER II clinical trial
COMPARE clinical trial

Ranger demonstrated consistently high primary patency versus uncoated PTA (RANGER II) and IN.PACT (COMPARE) at 12 months¹⁻²

Ranger patency versus PTA and IN.PACT
RANGER II clinical trial
COMPARE clinical trial

Ranger demonstrated similar primary patency to IN.PACT™ DCB, using around half the paclitaxel dose at 12 months²

Ranger low-dose patency versus IN.PACT

Ranger demonstrated a significantly lower 12-month CD-TLR rate versus uncoated PTA, resulting in a 67% relative reduction in repeat procedures¹

Ranger CD-TLR versus uncoated PTA
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References

1. Sachar R et al. RANGER II SFA Investigators. 1-year results from the RANGER II SFA randomized trial of the Ranger drug-coated balloon. JACC Cardiovasc Interv. 2021;10:1123–1133.

2. Steiner S, et al. COMPARE: prospective, randomized, non-inferiority trial of high- vs. low-dose paclitaxel drug-coated balloons for femoropopliteal interventions. Eur Heart J. 2020;41:2541–2552.

Caution:
The law restricts these devices to sale by or on the order of a physician. Indications, contraindications, warnings, and instructions for use can be found in the product labelling supplied with each device or at www.IFU-BSCI.com. Products shown for INFORMATION purposes only and may not be approved or for sale in certain countries. This material not intended for use in France.