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Europe, Middle East, Africa / Product Areas / Interventional Cardiology/Radiology / Peripheral Interventions / Pulsar-18

Pulsar^™18 Self-Expanding Stent System

Indicated for use in patients with atherosclerotic disease of the femoral and infrapopliteal arteries and for the treatment of insufficient results after Percutaneous Transluminal Angioplasty (PTA).*

Product Highlights

140 μm thin struts

Thinner than the leading brands¹

4F low profile

Improved acute outcomes vs. 6F²

Clinically proven^2,3

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

Technical Data
Ordering Information

Proximal Shaft
Catheter type	OTW
Recommended guide wire	0.018”
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 4.0 - 7.0 mm; L:20 - 200 mm
Proximal shaft	3.6F, hydrophobic coating
Usable length	90 cm and 135 cm

	Stent ø (mm)	Catheter length 90 cm Stent length (mm)
		20	30	40	60	80	100	120	150	170	200
4F	4	377456	377457	377458	377459	377460	366808	366809	3366810	366811	3366812
	5	377461	377462	377463	377464	377465	366813	366814	3366815	3366816	366817
	6	377466	377467	377468	377469	377470	366818	366819	3366820	366821	366822
	7	377471	377472	377473	377474	377475	366823	3366824	366825	366826	366827

	Stent ø (mm)	Catheter length 135 cm Stent length (mm)
		20	30	40	60	80	100	120	150	170	200
4F	4	377476	377477	377478	377479	377480	366828	366829	366830	366831	366832
	5	377481	377482	377483	377484	377485	366833	366834	366835	366836	366837
	6	377486	377487	377488	377489	377490	366838	366839	366840	366841	366842
	7	377491	377492	377493	377494	377495	366843	366844	366845	366846	366847

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:

1. 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.

Teleflex, the Teleflex logo, 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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