VIVO ISAR

Polymer Free Sirolimus Eluting Cobalt Chromium stent (Hybrid Cell Design) mounted on a rapid exchange PTCA Balloon Catheter. The Device is coated with a proprietary formulation of Sirolimus Drug in a Polymer Free Drug delivery matrix of Probucol (Matrix Builder) with Shellac Resin.

VIVO ISAR is the longest studied DES in terms of clinical data of Safety and Efficacy. VIVO ISAR has robust clinical data at 2,5 and 10 years published in indexed journals including high-risk Diabetes and STEMI patient subset.

A balloon expandable intra-coronary Cobalt Chromium stent platform. The unique microporous surface, called PEARL surface, is coated abluminal with Sirolimus and a biodegradable polymer coating. The stent surface has approximately 1 million micro-pores per cm2, average micro pore depth of approximately 2 µm and pore covers 100% of the surface. The microporous surface shows a trend towards a reduced rate of binary restenosis with equivalent safety, which proves that it is safe and feasible to use as a drug reservoir. *VIVO ISAR is the longest studied DES in terms of clinical data of Safety and Efficacy. VIVO ISAR has robust clinical data at 2,5 and 10 years published in indexed journals including high-risk Diabetes and STEMI patient subset.
The micro-porous surface allows a reduction of coating thickness to 3-5 µm

The Protégé DEB balloon catheter is a rapid exchange (Rx) catheter with a non-compliant and semi compliant balloon near the distal tip. The balloon is designed to provide an inflatable segment of known diameter and length at recommended pressures. During inflation, a controlled dosage of paclitaxel is delivered to the vessel wall. A balloon protector is placed over the balloon to maintain a low profile and an eyed stylet is placed into the inner lumen to protect the patency of the catheter. The catheter’s tip is tapered to facilitate advancement of the catheter to and through a stenosis or stent. The shaft has a hydrophilic coating. 

Supreme design for ULTIMATE Crossability and Deliverability

Supreme design for ULTIMATE Crossability and Deliverability

The device ADVA GLIDE - PTCA Balloon Catheter-Semi-Compliant, manufactured by AMS, is a Semi-compliant, rapid exchange, PTCA Balloon Catheter. There are 2 markers on the proximal shaft which aids in positioning of the catheter. The lumen of the catheter is used for inflating and deflating the balloon. The balloon material is Polyamide PA12.  

The device ADVA GLIDE - PTCA Balloon Catheter-Semi-Compliant, manufactured by AMS, is a Semi-compliant, rapid exchange, PTCA Balloon Catheter. There are 2 markers on the proximal shaft which aids in positioning of the catheter. The lumen of the catheter is used for inflating and deflating the balloon. The balloon material is Polyamide PA12.

The device NC ADVA GLIDE- PTCA Balloon Catheter- Non Compliant, manufactured by AMS, is a Non-compliant, rapid exchange, PTCA Balloon Catheter. There are 2 markers on the proximal shaft which aids in positioning of the catheter. The lumen of the catheter is used for inflating and deflating the balloon. The balloon material is Polyamide PA12.  

Ten‐Year Clinical Outcomes of Biodegradable Versus Durable Polymer New‐Generation Drug‐Eluting Stent in Patients With Coronary Artery Disease With and Without Diabetes Mellitus