Paris, May 24th, 2018 – ANGIOLITE Trial 12-month results revealed at Euro PCR 2018 ANGIOLITE Trial 12-month results were presented for the first time at Euro PCR by Dr. J. Moreu Burgos at the “Clinical outcomes with new DES” session. The randomized prospective multicentric controlled trial enrolled 223 patients and had the objective of demonstrating […]
2 Major Randomized Controlled Trials demonstrating benefits of leading iVascular products have been presented at Euro PCR 2018.
Paris, May 24th, 2018 – 2 Major Randomized Controlled Trials demonstrating benefits of leading iVascular products have been presented at Euro PCR 2018. Dr Moreu Burgos and Prof Ulf Teichgraber have shared the latest 12-month results of ANGIOLITE and EFFPAC RCTs in Paris, during the “Clinical outcomes with new DES” and “Hotline Peripheral and Stroke […]
iVascular will attend Euro PCR 2018 in Paris from May 22nd to 25th. We are looking forward to meeting you on our booth (F12) to learn more about the company innovations and proprietary technology. The latest clinical trials updates will be presented during the following scientific sessions. Thursday 24th of May 2018 at 2:45pm […]
London, April 25th, 2018 – EFFPAC RCT 12-month outstanding results with Luminor DCB have been revealed at CX Symposium 2018. The 12-month results from the full clinical cohort of the EFFPAC randomized controlled trial (RCT), were presented for the first time at CX Symposium 2018 at the DCB session on April 24th. Main objective was […]
Barcelona, March 8th, 2018 – EFFPAC-RCT 12-month results will be presented for the first time on April 24th at CX Symposium 2018 The 12-month results from the full clinical cohort of the EFFPAC randomized control trial (RCT), comparing the Luminor DCB (iVascular) to POBA, are going to be presented for the first time at Charing […]
Barcelona, February 14th, 2018 – iVascular Luminor DCB proves to be the best! The EFFPAC 6-month results have been presented by Prof. Dierk Scheinert (Park-Krankenhaus Leipzig, Germany) at the opening of the LINC 2018 main session dedicated to latest results with new technologies for femoropopliteal obstructions. EFFPAC is a Randomized Controlled Study comparing the Luminor […]
Oceanus 35, PTA balloon dilatation catheter receives CE Mark Approval for new catheter length of 200 cm.
Barcelona, December 28th, 2017- Oceanus 35, PTA balloon dilatation catheter receives CE Mark Approval for new catheter length of 200 cm. iVascular is pleased to announce that its Oceanus 35 PTA balloon dilatation catheter has received CE mark approval for its new usable catheter length of 200cm. With this, iVascular offers a complete portfolio including […]
Barcelona, December 18th, 2017- Luminor DCB has received approval for commercialization in New Zealand. IVascular is pleased to announce that the Luminor Drug Coated Balloon (DCB) indicated for peripheral arteries, has received approval for commercialization in New Zealand. Luminor is a Paclitaxel Coated Balloon specifically designed for dilatation of stenosis located in the iliac, femoral, […]
Barcelona, December 5th, 2017- iVascular starts partnership with TD Medical. In September of this year, TD Medical announced that in 2018 they will become exclusive distributors of iVascular in Netherlands. TD Medical stated “IVascular fully fits our objectives. They offer us the space to adapt to the dynamic changes in Dutch healthcare. This offers many […]
Barcelona, December 4th, 2017- Oceanus 14 Pro, PTA balloon catheter receives CE Mark Approval. iVascular is pleased to announce the release of the new Oceanus 14 Pro PTA balloon catheter, which has received CE Mark Approval to dilate stenoses in femoral, popliteal, and infrapopliteal arteries, and to treat obstructive lesions in arteriovenous dialysis fistulae. Oceanus 14 […]
Barcelona, September 25th, 2017 – iVascular S.L.U. has announced the initiation of the T.I.N.T.I.N. trial, evaluating the combined therapy of Luminor drug coated balloon (DCB) and iVolution self-expandable stent. T.I.N.T.I.N. study is prospective, investigator-initiated, non-randomized, multi-center trial, investigating the 12 months safety and efficacy of combined Luminor DCB and iVolution self-expandable stent in TASC C […]
Barcelona, September 21th, 2017 – iVascular S.L.U. has announced that Luminor 14m, the Drug Coated Balloon (DCB) indicated for below the knee BTK arteries, has received the Canadian Medical Device License (MDL). Luminor 14m is a Paclitaxel Coated Balloon specifically designed for BTK indications, thanks to its extra low crossing profile combined with TransferTechTM, iVascular […]