Terumo 25-1011 Runthrough NS Extra Floppy PTCA Guidewire 180cm Length .014" I.D. BX/5
Terumo 25-1011 Runthrough NS Extra Floppy PTCA Guidewire 180cm Length .014" I.D. BX/5 is backordered and will ship as soon as it is back in stock.
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Terumo 25-1011 Runthrough NS Extra Floppy PTCA Guidewire 180cm Length .014" I.D. BX/5
• Model: 25-1011
• Length: 180cm
• Diameter / Nominal Size: 0.014 in (≈ 0.36 mm)
• Tip Shape: Straight / shapeable distal tip
• Box of 5
The Terumo Runthrough NS Extra Floppy guidewire is engineered as a versatile “workhorse” coronary wire, aimed to navigate both routine and more challenging coronary lesions with consistent performance. Its critical advantage lies in the combination of a nitinol core that extends to the tip (core‑to‑tip) and the Direct Joint – Duo Core™ technology, which seamlessly fuses stainless steel and nitinol segments. This hybrid construction helps the wire deliver 1:1 torque response (the distal tip rotates in sync with the proximal end), enhancing steering precision and responsiveness in tortuous vessel paths.
To aid smooth traversal through complex vessel geometry, the distal ~24.8 cm is coated with Terumo’s proprietary “M‑coat” hydrophilic layer, reducing friction and improving trackability through curves and bends. Meanwhile, the very tip (~2 mm) is coated with silicone, offering tactile feedback to operators and providing a stable interface for devices (balloons, stents) to follow. The 3 cm radiopaque tip allows visual confirmation under fluoroscopy.
Because of its “Extra Floppy” tip design, the wire exerts minimal radial force on vessel walls, reducing the risk of vessel trauma, dissection, or perforation, especially in delicate or highly tortuous segments. Its softer tip suits crossing subtle side branches or navigating fragile anatomy. At the same time, the shaft’s balance of flexibility and pushability supports device delivery over the wire. In sum, the Runthrough NS Extra Floppy is intended to pair responsive handling, safety in complex anatomy, and broad applicability in interventional cardiology workflows.
This medical supply or implant item is not in its original equipment manufacturer (OEM) packaging but remains sterile and intact within its inner sterilization package. Despite the absence of the outer box, the item is unused and maintains sterility, ensuring it is suitable for medical use.
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