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Europe, Middle East, Africa / Product Areas / Interventional Cardiology/Radiology / Peripheral Interventions / Pulsar-35

Pulsar^™-35 Self-Expanding Stent System

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

Product Highlights

140 μm thin struts

Pulsar-35 struts are thinner than the leading brands.¹

Clinically Proven^¤2,3

Long term safety and efficacy (24-month data), even in calcified lesions^4,5

Tri-axial delivery system

Accurate stent deployment⁶

Technical Data
Ordering Information

Balloon catheter
Catheter type	OTW
Recommended guide wire	0.035”
Stent material	Nitinol
Strut thickness	140 μm
Strut width	85 μm
Stent coating	proBIO™ (Amorphous Silicon Carbide)
Stent markers	6 gold markers each end
Sizes	ø 5.0 - 7.0 mm; L: 30 - 200 mm
Proximal shaft	6F, hydrophobic coating
Usable length	90 and 135 cm

	Stent ø (mm)	Catheter length 90 cm Stent length (mm)
6F		30	40	60	80	100	120	150	170	200
	5	379878	379879	379880	379881	379917	379918	379919	379920	379921
	6	379883	379884	379885	379886	379922	379923	379924	379925	379926
	7	379888	379889	379890	379891	379927	379928	379929	379930	379931

	Stent ø (mm)	Catheter length 135 cm Stent length (mm)
6F		30	40	60	80	100	120	150	170	200
	5	379898	379899	379900	379901	379937	379938	379939	379940	379941
	6	379903	379904	379905	379906	379942	379943	379944	379945	379946
	7	379908	379909	379910	379911	379947	379948	379949	379950	379951

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.

Data on file. 6.0 mm diameters. Leading competitors have been selected based on the PV Stent Revenue Market Shares EU, 2017 and PV Revenue Market Shares APAC 2015; (Source: Millennium Research Group Inc.); 2. Bosiers M. et al. 4-French - compatible endovascular material is safe & effective in the treatment of femoropopliteal occlusive disease: Results of the 4EVER Trial. ENDOVASC THER 2013; 20: 746-756; 3. Lichtenberg M. Superficial Femoral Artery TASC D registry: 12-month effectiveness analysis of the Pulsar-18 SE nitinol stent in patients with critical limb ischemia. J Cardiovasc Surg (Torino). 2013 ; 54(4):433-9; 4. Lichtenberg et al. Effectiveness of the Pulsar-18 self-expanding stent with optional drug-coated balloon angioplasty in the treatment of femoropopliteal lesions - the BIOFLEX PEACE All-Comers Registry.Vasa (2019), 1-9. doi_10.10240301-1526a0007853. 5. Bosiers M. 4EVER 24 month results: long-term results of 4F Pulsar stent in femoropopliteal lesions. Presented at: CIRSE 2013; Barcelona, Spain; 6. Data on file. ¤Clinical outcomes of Pulsar-18 can be used to illustrate clinical outcomes of Pulsar-35 due to identical stent platforms

Teleflex, the Teleflex logo, and proBIO and Pulsar 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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