The BioMimics 3D Vascular Stent System is indicated to improve luminal diameter in the treatment of symptomatic de-novo or restenotic lesions in native superficial femoral and/or proximal popliteal arteries with reference vessel diameters ranging from 3.5 mm – 7.0 mm.
Stent Diameter (mm) |
Stent Length (mm) |
Reference Vessel Diameter (mm) |
Stent Delivery System OD (inch) |
Sheath Compatability* Fr/minimum ID (mm) |
Guidewire Compatability (inch) |
5 | 60,80,100,125,150 | 3.5 - 4.0 | 0.079 | 6FR/2.2mm | 0.035 |
6 | 60,80,100,125,150 | 4.0 - 5.0 | 0.079 | 6FR/2.2mm | 0.035 |
7 | 60,80,100,125,150 | 5.0 - 6.0 | 0.079 | 6FR/2.2mm | 0.035 |
Catheter Design | Over-the-wire |
Working Length | 113cm |
Shaft Profile | 6Fr / 2mm |
Sheath compatibility | 6Fr* (minimum iD of 2.2mm) |
Radiopaque markers | Radiopaque atraumatic system tip |
Distal tip outer sheath | |
Tantalum proximal system marker | |
Guidewire compatibility | 0.035" |
Stent material | Nickel-titanium alloy: nitinol |
Radiopaque markers number and location | 3 distal and 3 proximal |
Radiopacity | Excellent1 |
Fracture resistance | Excellent1 |
MRI compatibility | MRI conditional |
* Sheath compatibility evaluated with 6Fr Cordis™ Brite Tip and 6Fr TerumoRadifocus Introducer II sheath introducers.
1 – Zeller T. Oral Presentation VIVA 2014;
2 – Caro CG et al. 2013 J R Soc Interface10: 20130578
3, 4 – Data on file at Veryan Medical;
5 – Zeller T. et al; Circ Cardiovasc Interv. 2016;9
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