Astron Self-Expanding Stent System

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.*


Product Highlights

Clinically proven stent for the treatment of iliac disease1

Pull-back delivery system for simple stent deployment1

5.2F proximal shaft for contrast injection with device in sheath1

Stent
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
Stent
ø (mm)
Catheter length 70 cm
Stent length (mm)
30 40 60 80
6F 7 343773 343774 343775 343776
6F 8 343777 343778 343779 343780
6F 9 343781 343782 343783 343784
6F 10 - 349214 349215 349216
Stent
ø (mm)
Catheter length 120 cm
Stent length (mm)
30 40 60 80
6F 7 343785 343786 343787 343788
6F 8 343789 343790 343791 343792
6F 9 343793 343794 343795 343796

IFU Link

Refer to this IFU link for a copy of the Instructions for Use and for a complete listing of the indications, contraindications, warnings and precautions.

References:

*Indication as per IFU

  1. Data on file.

Teleflex, the Teleflex logo, Astron and proBIO are trademarks or registered trademarks of Teleflex Incorporated or its affiliates in the U.S and/or other countries. All other names are the trademarks or registered trademarks of their respective owners. Refer to this IFU link for a copy of the Instructions for Use and for a complete listing of the indications, contraindications, warnings and precautions. Information in this material is not a substitute for the product Instructions for Use. Not all products may be available in all countries.

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