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Clinically proven stent with pull-back delivery system and 5.2F proximal shaft

Indicated for use in patients with atherosclerotic disease of the iliac arteries and for the treatment of insufficient results after Percutaneous Transluminal Angioplasty (PTA), e.g. residual stenosis and dissection.*


Vascular Intervention Coronary Stent Systems

Product Highlights


Clinically proven stent for the treatment of iliac disease


Pull-back delivery system for simple stent deployment


5.2F proximal shaft for contrast injection with device in sheath

Clinically proven stent for the treatment of iliac disease¹

Designed to provide suficient chronic outward force and flexibility

Segmented stent design and strut thickness to provide sufficient chronic outward force in the iliac territory, while the peak-to-valley design and S-articulating connecting bars provide multi-directional flexibility and avoid fish-scaling in tortuous arteries

proBIO® silicon carbide coating reduces ion release by acting as an effective and reliable barrier to nickel and other heavy metal ion diffusion2

Pull-back delivery system for simple stent deployment

Pull-back delivery system enables simple stent deployment, while the easy release relieves friction of introducer valve on the retractable shaft during stent deployment, providing a smoother action

5.2F proximal shaft for contrast injection with device in sheath³

6F distal shaft with a 5.2F proximal shaft allows contrast injection while the device is positioned inside the introducer and across the lesion

Technical Data

Catheter type OTW
Recommended guide wire 0.035”
Stent material Nitinol
Strut thickness 225 μm (ø 10 mm = 230 μm)
Stent coating proBIO® (Amorphous Silicon Carbide)
Stent markers 4 gold markers each end
Sizes ø 7 - 10 mm; L: 30 - 80 mm
Proximal shaft 5.2F, hydrophobic coating
Usable length 70 and 120 cm

Ordering Information

ø (mm)
Catheter length 70 cm
Stent length (mm)
    30 40 60 80
6F 7.0 343773 343774 343775 343776
8.0 343777 343778 343779 343780
9.0 343781 343782 343783 343784
10.0 - 349214 349215 349216
ø (mm)
Catheter length 120 cm
Stent length (mm)
6F   30 40 60 80
7.0 343785 343786 343787 343788
8.0 343789 343790 343791 343792
9.0 343793 343794 343795 343796


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1. BIOFLEX I Astron Clinical Report; 2. Nickel release test result: J.M. Schmehl et al. / Cardiovascular Revascularization Medicine 9 (2008); 3. BIOTRONIK Data on file.

* Indication as per IFU. Astron and proBIO are trademarks or registered trademarks of the BIOTRONIK Group of Companies.