Peripheral Drug-eluting Stent System

OVERVIEW

Peripheral Drug-eluting Stent System

ZENFLEX® Pro Peripheral Drug-eluting Stent System, the 3rd peripheral drug-eluting medicated stentin the world, is designed especially for complex lesions and restenotic symptomatic lesions.

PRODUCT FEATURES

Peripheral Drug-eluting Stent System

Based on ZENFLEX Peripheral stent platform

UNIQUE STENT DESIGN

Open helical structure

Segmented MicroMesh design

Offset Peak-Valley design

Results in superior flexibility and great radial force of the stent

Promises immediate wall apposition and precise stent placement

Polymer free Coating

The special ZENFLEX® Pro coating technology is a ultrasound spray crystalline paclitaxel.

Uses a special auxiliary gas to recrystallize the drug coating and obtain a stable uniform drug coating layer bonded on the stent surface.

Free from any polymer, adhesive, or excipient, while eliminating the potential risks that polymers may cause.

Provides the effective Paclitaxel tissue concentration within 90 days, and the stent converts into bare stent with complete drug delivery after 180 days

ORDERING INFORMATION

Usable Length(80cm)	Usable Length(125cm)	Stent Length(mm)	Stent Diameter(mm)	Sheath
ZX05020080A	ZX05020125A	20	5	6F
ZX05030080A	ZX05030125A	30
ZX05040080A	ZX05040125A	40
ZX05060080A	ZX05060125A	60
ZX05080080A	ZX05080125A	80
ZX05100080A	ZX05100125A	100
ZX05120080A	ZX05120125A	120
ZX05150080A	ZX05150125A	150
ZX06020080A	ZX06020125A	20	6	6F
ZX06030080A	ZX06030125A	30
ZX06040080A	ZX06040125A	40
ZX06060080A	ZX06060125A	60
ZX06080080A	ZX06080125A	80
ZX06100080A	ZX06100125A	100
ZX06120080A	ZX06120125A	120
ZX06150080A	ZX06150125A	150
ZX07020080A	ZX07020125A	20	7	6F
ZX07030080A	ZX07030125A	30
ZX07040080A	ZX07040125A	40
ZX07060080A	ZX07060125A	60
ZX07080080A	ZX07080125A	80
ZX07100080A	ZX07100125A	100
ZX07120080A	ZX07120125A	120
ZX07150080A	ZX07150125A	150

If you want to know more types of paclitaxel stent, please visit our website.

Zylox TonbridgeMedical Technology Co., Ltd. ("Zylox-Tonbridge" or "the Company", "2190.HK") announced on February 28 that it has received approval from Hong Kong Stock Exchange, regarding implementation of full circulation of its H shares. The approval was for the conversion and listing of the Company’s 194 million domestic unlisted shares.

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