It is designed to ​dilate stenotic lesions in the iliac, femoral, ilio-femoral, ​popliteal, infra-popliteal, and renal arteries.

In addition, it is indicated for treating obstructive ​lesions in native or synthetic arteriovenous ​dialysis fistulae, as well as for stent post-dilatation in the peripheral vasculature. ​

The guidewire lumen measures 30 cm for ​balloon lengths of 20–150 mm, and 40 cm for the 200 mm option. ​ Hydrophilic coating spans 28 cm for balloons of 20–150 mm, and 38 cm for the 200 mm balloon. The catheter shaft diameter is 3.5 Fr (1.16mm). ​

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• Stiff core wire for improved pushability^{1 ​}

designed to reach and cross very distal target lesions. ​

• ​Low-profile balloon design¹ and hydrophilic coating ​

facilitate lesion access and crossing for below-the-knee and below-the-ankle interventions. ​

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Here you can find a comprehensive summary of guidewire and sheath compatibility, ​balloon folding configuration, and the nominal and rated burst pressure specifications ​of the Crosperio™ RX Balloon Dilatation Catheter. ​

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Please use the corresponding reference codes provided in the ordering table when placing your order.​

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^{Disclaimer​}

^{Not all products are available for sale in all countries. This information is provided only in respect to markets where these products are approved or cleared. Please contact your Terumo local sales representative for more information. Refer to Instructions for Use for contraindications, warnings, precautions and additional information. All brand names are trademarks or registered trademarks owned by TERUMO CORPORATION, its affiliates, or unrelated third parties.​}

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